Hao Liang
Yang Liu1,2†
Xiaoyi Zhang
Jun Chen- 1Department of Urology, Qilu Hospital of Shandong University, Jinan, Shandong, China
- 2Department of Urology, Weifang People’s Hospital, Weifang Medical University, Weifang, Shandong, China
- 3Department of Immunology, School of Basic Medical sciences, Weifang Medical University, Weifang, Shandong, China
Prostate cancer is one of the most common malignant cancers of the male genitourinary system and has high morbidity and mortality. Currently, treatment modalities for localized prostate cancer focus mainly on radical prostatectomy or radical radiation therapy. Some patients still experience disease recurrence or progression after these treatments, while others are already at an advanced stage or have metastases at the time of diagnosis. With the continuous development and progress of medicine in recent years, immunotherapy has become a revolutionary cancer treatment, and has achieved remarkable accomplishments in the treatment of hematologic malignancies. A variety of immunotherapies have also appeared in the field of advanced prostate cancer treatment, including therapeutic vaccines and immune checkpoint therapies. Despite the discrepancy between the results of some immunotherapy studies, immunotherapy for prostate cancer has shown some initial success, especially in combination immunotherapies. Currently, immunotherapy is mainly used in advanced prostate cancer, especially in patients with metastatic castration-resistant prostate cancer. However, with the development of more clinical trials of immunotherapy, more evidence will be provided supporting the rational application of immunotherapy in the future.
1 Introduction
Prostate cancer is one of the most common cancers among men worldwide, with an incidence of 1.4 million new cases per year. Approximately ten million men currently have prostate cancer worldwide, of which about 700,000 have metastasis, causing about 400,000 deaths each year (1, 2).
Current guidelines recommend radical prostatectomy or radiation therapy for early-stage localized prostate cancer (3–6). Some patients still experience disease recurrence or progression after treatment (7). For hormone-sensitive prostate cancer that responds to endocrine therapy, androgen-deprivation therapy (ADT) is typically maintained. Patients have a high response rate when they are initially treated with ADT, but long-term ADT leads to drug resistance. Androgen receptor (AR) amplification, AR mutation, AR splice variation, and the emergence of compensatory pathways are possible resistance mechanisms. Studies have shown that within 1–3 years of ADT, most patients experience progression of the cancer to metastatic castration-resistant prostate cancer (mCRPC), which defines patients who are at an advanced stage of the disease (8). The 5-year survival rate for patients with mCRPC is approximately 30% (9). Compared with conventional examinations such as CT and bone scan, the new PSMA-PET/CT and FDG-PET/CT have higher sensitivity for metastases, especially in patients with lower PSA levels (10–12). The advancement of imaging technology has further increased the number of mCRPC patients. Currently, a variety of drugs have been approved for the treatment of patients with mCRPC, such as the new generation of AR signaling inhibitors, chemotherapy drugs, bone-targeted therapy drugs, and poly-ADP-ribose polymerase (PARP) inhibitors (13). However, mCRPC remains an incurable fatal disease. In recent years, many new drugs have been approved for the treatment of hormone-sensitive prostate cancer (HSPC), and reports of cross-drug resistance in mCRPC patients have attracted wide attention (14), prompting us to explore a new, safer, and more effective cancer treatment. Immunotherapy for malignancies has achieved exciting results and a series of exploratory studies on immunotherapy for prostate cancer have been conducted. Immunotherapy enhances the immune system’s ability to recognize and kill cancer cells by regulating the autoimmune system, improving the antigen presentation ability, destroying the inhibitory tumor microenvironment, and reducing the apoptosis of effector cells to achieve the purpose of anti-tumor therapy (15–17). Prostate cancer has unique tumor characteristics compared to other tumors. First, it expresses multiple tumor-associated antigens: e.g., prostate-specific antigen (PSA), prostate-specific membrane antigen (PSMA), and prostate stem cell antigen (PSCA), which provide a reliable therapeutic target for prostate cancer immunotherapy (18–20). Second, the relatively “inert” tumor growth characteristics of prostate cancer also provide an extended window for cancer immunotherapy to establish an effective immune response. However, prostate cancer is a “cold” tumor that lacks immune cell infiltration (21). The low number of lymphocytes and the predominance of immunosuppressive components in the tumor microenvironment may limit the efficacy of immunotherapy (22, 23).
We review current research advances, clinical applications, and the risks and challenges related to prostate cancer immunotherapy. Most of these studies have been conducted in patients with advanced prostate cancer represented by mCRPC, so this will help us to understand some of the latest progress in the field of immunotherapy for advanced prostate cancer.
2 Therapeutic vaccine
There are various types of vaccines for prostate cancer treatment currently available, including cellular vaccines, viral vaccines, DNA vaccines, and other classifications, and in this section, we will present several representative vaccines.
Sipuleucel-T: first introduced in April 2010 and was the first therapeutic cancer vaccine approved by the Food and Drug Administration (FDA), primarily for use in asymptomatic or minimally symptomatic patients with mCRPC (24). The vaccine utilizes leukocyte isolation technology to isolate monocytes from the peripheral blood of the patient, which are cocultured in vitro with a recombinant fusion protein (PA2024) of prostatic acid phosphatase (PAP) and colony-stimulating factor (GM-CSF). granulocyte-macrophage. PA2024 stimulates the maturation of monocytes into dendritic cells that specifically present PAP. Dendritic cells activate PAP-specific cytotoxic T cells in patients after transfusion, enhancing their ability to recognize and kill prostate tumor cells. The results of the IMPACT phase III clinical trial (NCT00065442) demonstrated a survival benefit of Sipuleucel-T (25), compared to the placebo group, it prolonged the median overall survival (OS) of mCRPC patients by 4.1 months (median OS: 25.8 vs 21.7 months) and reduced the risk of death by 22%, hazard ratio (HR): 0.78, 95% CI: 0.61–0.98. This is consistent with another study showing an OS benefit of 4.5 months with Sipuleucel-T (26). However, there was no improvement in the time to disease progression. The study observed a more significant benefit in patients with low tumor load, suggesting a more significant OS benefit with early use of Sipuleucel-T in mCRPC patients. Similarly, an inverse association between PSA level and OS benefit was also seen in PROCEED study (27). Sipuleucel-T also exhibits a satisfactory safety profile, with studies reporting common adverse events (AEs) such as chills, fever, headache, muscle pain, and flu-like symptoms, which were associated with cytokine release after infusion. 65.2% of AEs were G1-G2, and most symptoms lasted no more than 2 days. Only 0.9% of the patients did not complete the infusion because of infusion-related adverse reactions (21). Several studies have recently been conducted to explore combination therapy regimens of Sipuleucel-T to analyze the most significant therapeutic benefit of Sipuleucel-T (28). It is still uncertain whether combination therapy can provide more benefit to specific groups, and we will introduce it in the subsequent combination therapy section of the article.
PROSTVAC: PROSTVAC is composed of a heterologous prime-boost regimen using two different live poxviral-based vectors: PROSTVAC-V, a recombinant vaccinia virus, and PROSTVAC-F, a recombinant fowlpox virus. The two vectors contain transgenes for human PSA and three costimulatory molecules (TRICOM: b7.1, LFA-3, ICAM-1). In phase II clinical trials (29), PROSTVAC prolonged median OS by 8.5 months and reduced the risk of death by 44% compared with placebo control, and corrected data expanded the survival benefit (median OS: 26.2 vs 16.3 months) and the survival advantage (HR=0.50) (30). Regarding safety, most AEs reported by PROSTVAC were local injection reactions, with fewer systemic AEs. The phase III PROSPECT trial compared patients treated with PROSTVAC+GMC-CSF, PROSTVAC alone, and placebo to further examine the effects of treatment (31). Contrary to the positive results of the phase II clinical trial, neither of the treatment groups effectively improved OS in the interim analysis, and the alive without events (AWE) rate was similar in both groups at six months. Events including radiographic progression, pain progression, initiation of chemotherapy for prostate cancer, or death, forced early termination of the trial. Regarding the differences in efficacy shown in the PROSPECT trial, an imbalanced allocation of prognostic-related factors in the phase II trial, may have amplified the benefits of OS in the treatment group; also, the smaller number of patients and possible observer bias may have affected the results. Additionally, including patients with multiple prior life-prolonging treatments in the PROSPECT trial may have influenced the positive outcome. Although the results of the phase 3 trial did not meet expectations, the PROSTVAC combination therapy study is still ongoing, and a study (NCT02933255) is exploring the safety and efficacy of PROSTVAC in combination with Nivolumab, and these combination therapies will provide more evidence on the appropriate use of PROSTVAC in the future (32, 33).
DCVAC/PCa is an active immunotherapy based on the activation of antitumor immunity by autologous dendritic cells. Dendritic cells are isolated from mononuclear cells in the peripheral blood of the patient by leukapheresis and brought into contact with dead human prostate adenocarcinoma cell lines, thus enhancing their antitumor activity. A single-arm phase I/II clinical trial in mCRPC patients confirmed that DCVAC/PCa combined with chemotherapy had a good safety profile. No serious adverse events (SAEs) related to DCVAC/PCa were reported in the study, and the median OS was 19 months, which was significantly improved compared with the predicted value of Halabi and MSKCC nomograms (34). Another study demonstrated that DCVAC/PCa produced durable immune responses and significantly prolonged PSA doubling time (PSADT) in prostate cancer patients with low tumor burden (35). The study also reported that the common AEs of DCVAC/PCa were local injection site reactions, fatigue, influenza like-illness, and mild infections, all of which were G1-G2. However, the VIABLE trial (NCT02111577) reported different results (36), with no significant OS benefit in the DCVAC/PCa combination chemotherapy group compared to the placebo group. No difference was observed in either of the primary efficacy endpoints. The VIABLE trial further provided good safety evidence for DCVAC/PCa, with most treatment-related AEs (TRAEs) associated with chemotherapy rather than DCVAC/PCa. The 119 patients who did not develop DCVAC/PCa were included in the efficacy analysis of the VIABLE trial. However, the shorter OS in this group of patients weakened the DCVAC/PCa treatment effect. Study found a dose-dependent treatment effect, with a subgroup of patients receiving more than ten doses of vaccine showing a propensity to benefit OS. Studies evaluating the efficacy of DCVAC/PCa in prostate cancer are still lacking, and more studies are needed to confirm its potential therapeutic value.
pTVG-HP[MVI-816] is a DNA vaccine that encodes the human PAP cDNA. pTVG-HP[MVI-816] has been previously studied for its favorable safety profile in patients with early PSA recurrent prostate cancer, and enhanced vaccine-induced PAP-specific Th1 cell responses have been observed (37). There are no reports on the efficacy and safety of the pTVG-HP[MVI-816] vaccine alone in large trials in patients with mCRPC. In the phase II clinical trial of non-metastatic hormone-sensitive prostate cancer (nmHSPC) with biochemical recurrence (38), there was no significant difference in 2-year metastasis-free survival (MFS) in the pTVG-HP[MVI-816] group (41.8% vs 42.3% P=0.97). Regarding secondary endpoints, no significant differences were observed between the two groups in median MFS and median PSADT; partial immune responses were observed early in treatment but then disappeared. Difficulty in maintaining long-term immune responses may be the main obstacle limiting the antitumor efficacy of pTVG-HP. There is no substantial evidence to support that a single regimen of MVI-816 may make a meaningful difference for patients, and we are counting on whether a combination regimen can enhance its efficacy. A recently published study comparing the effectiveness of MVI-816 in combination with pembrolizumab in patients with mCRPC reported a preliminary exploration of the optimal dosing regimen for combination therapy. The results showed that the combination therapy was superior to PD-1 or PD-L1 monotherapy in PSA declines, tumor volume decreases, and 6-months DCR, while the combination therapy had a good safety profile. G2 or higher TRAEs occurred in 42% of the patients, and common TRAEs were thyroid dysfunction, adrenal insufficiency, colitis, and hepatitis (39). Another DNA vaccine, pTVG-AR [MVI-118], which contains cDNA encoding the ARligand-binding domain (AR-LBD), has been evaluated in a completed multicenter phase Ι trial (NCT02411786) and showed a favorable safety profile and durable immune responsiveness (40).
In summary, durable immune responses specific to tumor antigens have been observed in studies of multiple prostate cancer therapeutic vaccines. However, there is still a lack of consistent clinical evidence confirming the therapeutic efficacy of vaccines, except for Sipuleucel-T, for which several recent large trials have provided conflicting results. Vaccine combination therapy appears to have gained more attention in recent years, which may provide new approaches for subsequent treatment and provide a rationale guiding and supporting the exploration and use of prostate cancer vaccine therapy.
3 Immune checkpoint therapy
There are antagonistic mechanisms of promotion and suppression of the immune system in the development of tumors: Conversely, when some activating signals stimulate cytotoxic cells with tumor-killing capacity, they will promote functional phenotype transformation and accelerate cell proliferation, which can enhance their ability to kill cancer cells. Conversely, when cytotoxic cells are stimulated by inhibiting signals from the surrounding environment, they will cause their dysfunction and inhibit their proliferation, thus weakening their ability to kill tumor cells. Cells exhibit negative regulatory function via a receptor or ligand called an immune checkpoint, and anti-tumor therapy targeting the regulating of immune checkpoints is called Immune Checkpoint Therapy (ICT) (41, 42). Food And Drug Administration (FDA) has approved ICT for the treatment of solid malignancies in multiple organs (43–45). The main therapeutic targets of ICT in prostate cancer are the cytotoxic T lymphocyte-associated antigen 4 (CTLA-4), programmed cell death protein 1 (PD-1) and its ligand (PD-L1) (46, 47).
Ipilimumab is a humanized monoclonal antibody that blocks CTLA-4 and enhances the immune effect of T cells. It was approved in 2011 for the treatment of melanoma (48). Some early clinical trials that confirmed the anti-tumor activity of Ipilimumab in solid tumors included patients with prostate cancer. However, the results of a phase III trial in patients with asymptomatic or minimally symptomatic mCRPC without visceral metastases who had not previously been treated with chemotherapy (49), did not show a benefit in OS following treatment with ipilimumab compared to placebo. In a separate phase III study (50), the ipilimumab group did not show any significant OS benefit compared with placebo in a population of minimally symptomatic mCRPC patients who had received prior docetaxel chemotherapy and were chemotherapy-sensitive, despite the presence of long-term responders. However, we found that a small group of patients in this study achieved a significant and sustained clinical response with ipilimumab. A follow-up study found that a subgroup of patients with mCRPC with immune characteristics such as higher intratumor infiltrating CD8+ T cells, high IFN-γ response gene signals, and more robust antigen-specific T cell responses was more likely to achieve control of progression with ipilimumab monotherapy and more extended survival benefits, despite the relatively low tumor mutational load in this subset of patients (51). This finding indicates that a more careful selection of appropriate patients is required for ipilimumab treatment.
PD-1 is expressed in activated T cells and binds to PD-L1 and PD-L2 to mediate inhibition of the activity of variable tumor effector cells (52). In patients with metastatic melanoma, objective response rates (ORR) ranging from 20% to 45% were observed after CTLA-4 or PD-1 (53), with response rates up to 60% observed when CTLA-4 was combined with PD-1 blockade (54, 55). However, similar to ipilimumab monotherapy, studies have found that nivolumab and pembrolizumab alone do not achieve the expected treatment outcomes in patients with advanced prostate cancer (56–58). In the KEYNOTE-199 trial (58), the ORR (5% vs 3%) and disease control rate (DCR) (13% vs 18%) in PD-L1-positive patients were similar to the PD-L1-negative patient group; no differences in OS were observed between the two groups, which may be related to the more advanced stage of the disease in the positive PD-L1 group. It is believed that the immunosuppressive tumor microenvironment, tumor mutation burden and immune escape mechanism of prostate cancer are the reasons that hinder the efficacy of immune checkpoint inhibitors (59). At the same time, the shorter duration of treatment in KEYNOTE-199 could diminish the OS benefit. Previous studies have found that ipilimumab treatment significantly increased the number of tumor-infiltrating T cells in prostate cancer patients. However, it induced a compensatory immunosuppressive pathway mediated by PD-1/PD-L1 signaling, negatively affecting antitumor therapy (60). Based on this finding, the subsequent CheckMate650 Phase II trial (NCT02985957) focused on improving treatment outcomes for patients with prostate cancer when ipilimumab was administered in combination with nivolumab (61). We will describe this study in more detail below with regard to the combination therapy strategies. The European Association of Urology (EAU) guidelines suggest that pembrolizumab may be a valuable additional management strategy for mCRPC patients with high microsatellite instability, and with continuous advances in genome sequencing technology, it will be helpful to screen patients who can benefit from immunosuppressive therapy (62, 63).
The difficulty of producing substantial clinical benefits with ICT alone in unselected patients with prostate cancer has been widely recognized. However, earlier studies have reported that a subgroup of prostate cancer patients with defects in the DNA mismatch repair gene and high microsatellite instability characteristics tended to have higher response rates to single ICT (64, 65). The results of the subgroup analysis also suggested that single immunological checkpoint blockade had better efficacy in these patients. However, this idea has been questioned in recent studies: it has been shown that there is no positive correlation between CD8+ T cell numbers and neoantigen load in breast and prostate cancers and that the characteristics of high tumor mutational load is not predictive of the efficacy of ICT in patients with breast and prostate cancer. Therefore, the search for additional biomarkers as predictors of immune checkpoint efficacy may be required in the future (66, 67). This highlights the importance of tumor signature screening for prostate cancer patients and individualized treatment regimens for prostate cancer in terms of immunotherapy strategies.
4 Adoptive cell therapy
Adoptive cell therapy is a rapidly expanding field of medicine in recent years that mediates antitumor, antiviral, or anti-inflammatory effects by isolating, modifying, and expanding autologous or allogeneic tumor-responsive lymphocytes and reinfusing processed lymphocytes back into the patient (68, 69). Of these, cell therapies involving chimeric antigen receptor T (CAR-T) have demonstrated high response rates and durable disease remission in the treatment of hematologic malignancies (70–72), and several companies have received FDA approval for their CAR-T products for the treatment of refractory and complex hematologic diseases in the last 5 years (73).
CAR-T therapy genetically modifies T cells by in vitro transfection technology to express engineered chimeric receptors (74). Currently, CAR-T technology has developed to the fourth generation, as the latest generation technology, the structure not only has a co-stimulatory protein intracellular domain but also promotes the release of cytokines such as IL-12, IL15, and IL18 after receptor activation, which can enhance the killing efficiency of T cells (75). When CAR-T cells are cultured and expanded in vitro and transfused back to patients, the transmembrane region converts the CAR recognition signal for extracellular targeted tumor antigens into a signal for activation of T cells through the intracellular domain. When CAR-T cells arrive inside the tumor, they cause cytotoxic particles such as cytokines and perforins to be secreted by cytotoxic T cells, leading to the destruction of tumor cells (76). This technique is being applied to treat solid malignancies, including prostate cancer (77, 78). This is a new T cell-mediated antitumor therapy in which cytotoxic T cells can be activated independently of major histocompatibility complex (MHC), thus eliminating dependence on the traditional T cell receptor-MHC pathway, can be severely compromised in the “cold” tumor microenvironment of prostate cancer (79).
Narayan et al. reported the results of the latest phase I clinical trial of CAR-T therapy in patients with mCRPC (80): In terms of safety, a cytokine release syndrome (CRS) was the most common drug-related SAEs, predominantly G1-3, and most patients exhibiting a CRS resolved spontaneously or with symptomatic treatment, confirming its good safety profile. In terms of tumor responsiveness, PSA levels decreased by at least 30% in 4 of the 13 patients; one patient had a >98% decrease in PSA levels accompanied by significant proliferation of CAR-T cells in vivo, and 38.5% of patients maintained stable disease status at three months posttreatment assessed by imaging. The study showed a median OS of 15.9 months and a median progression free survival (PFS) of 4.4 months in patients receiving CAR-T therapy. Although a general immune response was observed in the study, it does not seem to translate into a survival benefit for mCRPC patients. The study also observed that patients had a dose-dependent decrease in peripheral blood CAR-T cell proliferation, inflammatory cytokine expression, clinical CRS, and PSA, which could help guide the appropriate dose selection for future CAR-T therapies in clinical applications (81). This result is generally consistent with the results of the earlier P-PSMA-101-001 trial (NCT04249947). Currently, there is no consensus on whether to receive lymphatic clearance prior to CAR-T therapy, and studies have shown that lymphatic clearance enhances T cell proliferation and viability, thus improving efficacy but also increasing hematologic and systemic toxicity. Thus, more research is needed to select suitable patients to receive lymphatic clearance to achieve maximum therapeutic benefit.
Although CAR-T therapy has shown good therapeutic potential in the treatment of advanced prostate cancer, several barriers remain to be addressed to enhance CAR-T therapy efficacy in solid tumors: 1) physical interference of CAR-T cells by the stroma surrounding solid tumors; 2) abnormal CAR-T function due to the specific suppressive tumor microenvironment of prostate cancer; and 3) CAR-T cell defects: reduced self-replication ability (82, 83). Multiple studies of CAR-T therapies are ongoing (NCT03873805; NCT02744287). A preclinical study has shown that CAR-T combined with docetaxel has synergistic efficacy (84), and this feasibility needs to be supported by evidence in future clinical trials. With the improvement of the structure of CAR-T cells, as well as the determination of therapeutic dose and treatment cycle, CAR-T may become an alternative treatment for prostate cancer patients.
5 Bispecific antibody therapies
Bispecific antibody therapies, especially bispecific T-cell engagers (BiTE) (85), have shown significant therapeutic promise in the treatment of refractory hematologic malignancies. Recently, BiTE therapies have been explored to treat advanced malignant solid tumors. The studies conducted to date have mainly included patients with mCRPC. BiTEs utilize single chain variable fragment (ScFv) technology to recognize specific tumor antigens. Antibodies on one side of the BiTE bind specifically to tumor cell surface tumor antigens, such as PSMA, generating activation signals delivered to the T cell CD3 surface receptors via antibodies on the other side (86). Direct engagement of co-stimulatory CD3 receptors bypasses the need for traditional monosynaptic binding and enables MHC non-dependent T cell activation. In recent preclinical studies (87), AMG160 showed promising durable specific antitumor activity and an acceptable nonclinical safety profile in a model of prostate cancer tumor graft. There is a lack of solid evidence supporting the clinical application of BiTE in large trials, with safety and efficacy results of BiTE in patients with prostate cancer reported only in phase I clinical trials (88). In terms of imaging, there is evidence that AMG160 does not interfere with the signal intensity of 68Ga-PSMA-11PET/CT compared to non-PSMA specific BiTE, which has important implications for the post-treatment efficacy assessment (89). BiTE is more readily available for widespread use than CAR-T therapy because it is not a separately produced cellular product. In terms of tumor penetration capacity, BiTE therapy is superior to CAR-T, and in terms of safety, the incidence of BiTE adverse events is lower and relatively controllable. However, there are still many challenges for BiTE therapy, such as loss of target antigen, formation of resistant antibodies, and up-regulation of immune checkpoints (90, 91). The up-regulation of immune checkpoint is a possible resistance mechanism of BiTE, which provides theoretical support for the combination of BiTE therapy and ICI (92). In addition to targeting PSMA, exploring other alternative tumor antigens, such as PSCA, disintegrin and metalloproteinase 17 (ADAM17M) and delta-like ligand 3 (DDL3), may also be a future direction (93–95).
6 Combination therapy
Current evidence shows that treatment with single immunotherapy regimens appear have not achieved the expected therapeutic effects. With the increasing understanding of the regulatory mechanisms of immunotherapy in various preclinical studies, immunotherapy-based combination therapy strategies are gradually becoming and increasing trend. Current combination treatment options include the combination of multiple immunotherapy regimens, immunotherapy combined with hormone therapy, immunotherapy combined with radiation therapy, and immunotherapy combined with chemotherapy.
6.1 Immune dual combination therapy
Uncertainty about the efficacy of immune checkpoint therapy monotherapy regimens facilitated the exploration of combination regimens, and the establishment of the CheckMate650 phase II trial (NCT02985957) (61). The no-chemotherapy cohort and the post-chemotherapy cohort received ipilimumab (3 mg/kg) in combination with nivolumab (1 mg/kg) with a median follow-up of 11.9 months and 13.5 months, respectively, ORR of 25% and 10% in the two groups, and median OS of 19.0 months and 15.2 months, respectively. Although combination therapy demonstrated significant treatment effects, the study reported a significantly increased incidence of TRAEs, with approximately 40% of patients in both groups requiring the application of high-dose cortisol for immune-mediated AEs. Approximately half of the patients exhibited G3-G4-grade TRAEs and 4 patients experienced TRAE-related deaths. Higher drug-related mortality in patients with mCRPC compared to the same dose regimen previously applied in patients with metastatic melanoma may be associated with advanced age and worse ECOG scores. The significant treatment effect observed in the CheckMate650 trial revealed the therapeutic promise of dual immunosuppressant combinations, and a concomitant increase in drug toxicity needs to be investigated in future studies. We must explore different dosing strategies to find the balance between efficacy and toxicity. The other study investigated the combination of Sipuleucel-T and Ipilimumab in patients with mCRPC, and the combination did not achieve greater efficacy than Ipilimumab monotherapy, which is similar to the results of the previous study (96, 97). It was found that the timing of Ipilimumab administration after Sipuleucel-T vaccination may affect the activation of antigen-specific T cells, but no differences in patient survival benefit and disease progression were observed. Similarly, no additional benefit was shown with Sipuleucel-T plus pTVG-HP as an immune-boosting regimen (98).
6.2 Immunotherapy combined with hormone therapy
Hormone therapy plays an important role in the treatment strategy of prostate cancer patients, and the new generation of AR pathway inhibitors provide more options to treat patients with advanced prostate cancer (99, 100). In recent years, as the mechanisms of androgen activity in prostate cancer have been studied, we have gained a richer understanding of the immune regulatory mechanisms played by androgens and AR in patients with prostate cancer. AR is expressed not only in tumor cells but also in various immune cells in vivo, playing an immunomodulatory role (101, 102). Androgens have long been known to inhibit the development and activation of T and B cells through multiple mechanisms (103). In patients with prostate cancer, immunotherapy combined with hormone therapy has emerged as a new combination therapy. However, the efficacy of immunotherapy combined with hormone therapy in patients with prostate cancer has produced uncertain findings. Conflicting treatment outcomes are usually attributed to differences in patient populations. Recent studies have found that AR antagonists interfere with initial T cell activation and may diminish the therapeutic effect of combination therapy (104). However, this immunosuppressive effect can be avoided by judicious selection of the sequential dose timing (105, 106). A recent study published in Nature revealed a potential mechanism by which AR antagonists in combination with anti-PD-1 monoclonal antibodies in clinical trials led to high patient responsiveness (105). The study reported that enzalutamide prevented T cell depletion by inhibiting AR in CD8+ T cells while increasing IFN-γ release and improving responsiveness to targeted PD-1 therapy, which provided a theoretical basis for the administration of hormone therapy in combination with immune checkpoint inhibitors. The IMbassador250 trial (NCT03016312) investigated the impact of co-administration of atezolizumab with enzalutamide compared to enzalutamide alone on the survival benefit of patients with mCRPC (107). Although the incidence of AEs in the combination group was essentially identical to enzalutamide alone, the combination group (median OS: 15.2 months) did not show a survival benefit compared to enzalutamide alone (median OS: 16.6 months) (HR=1.12 95% CI 0.91–1.37), forcing the early termination of the study. In terms of secondary outcomes, the combination group similarly did not show any benefit. It is difficult to provide a plausible explanation for the IMbassador250 trial results. However, previous single-arm studies have found that pembrolizumab combined with enzalutamide produced an 18% response rate in unselected mCRPC. In the latest Nature study, the ADT+enzalutamide+anti-PD-L1 triplet regimen provided a superior OS benefit and the most significant reduction in tumor volume in prostate cancer and sarcoma models compared to the duplex regimen, and it appears that ADT enhanced the synergistic effect of enzalutamide in combination with immunotherapy. A clinical trial of triple combination therapy ADT + enzalutamide + pembrolizumab (NCT04191096) is underway in patients with mHSPC, which will further validate the safety and patient responsiveness of the triple combination regimen. We cannot help but look forward to the therapeutic potential of the triple combination regimen for advanced prostate cancer.
6.3 Immunotherapy combined with radiation therapy
Radiation therapy has been one of the practical tools for the treatment of various malignant tumors, and it can stimulate the production of tumor-specific immune responses by inducing tumor cell death, enhancing the release of tumor-associated antigens, and upregulating the expression of tumor suppressor proteins and cytokines through various pathways and mechanisms (107, 108). In recent years, targeted radiotherapy, represented by Ra-223, has gradually gained clinical popularity as an emerging therapeutic tool for patients with advanced prostate cancer, especially for those with combined bone metastases (109). Ra-223 is a radioactive calcium analogue that selectively binds to areas of increased bone transformation and has a certain degree of “bone targeting”. It produces antitumor effects by releasing alpha particles into surrounding tissues to destroy cellular DNA. Due to the small diameter of the action of the alpha particle (2–10 cell diameters), Ra-233 causes less damage to surrounding normal tissues, giving it a better safety profile (110). In 2013, Ra-223 was approved by the FDA for the treatment of patients with symptomatic mCRPC with bone metastases (111). The survival benefit and the improvement of bone-related events in mCRPC patients have been supported by the results of several large clinical trials, in which Ra-223 significantly prolonged OS and PFS in patients with advanced prostate cancer, reduced bone pain symptoms considerably, and delayed the onset of bone-related events during treatment (112, 113). Several trials have recently explored the feasibility of a combination immunotherapy regimen with Ra-223. A recently completed trial of Sipuleucel-T in combination with Ra-223 demonstrated superiority to Sipuleucel-T administered alone in patients with mCRPC with bone metastases (114). The study found that Sipuleucel-T in combination with Ra-223 did not increase the incidence or severity of adverse events; however, the combination group did not demonstrate an advantage in secondary outcome indicators related to the immune response. The combination group showed higher PSA responsiveness (33% vs 0%) and longer time to tumor progression in the observation of patient clinical outcomes (median PFS 39w vs 12w; HR=0.32), which was consistent with the findings obtained in previous studies (115), in which Sipuleucel-T combined with Ra-223 produced a more significant benefit in patients with mCRPC without additional toxicity. However, not all combination therapies with Ra-223 produced exciting results; for example, trials exploring the administration of atezolizumab in combination with Ra-223 did not produce any additional therapeutic benefits in the combination group but instead resulted in more significant drug toxicity in the combination group compared to monotherapy, Thus, combination therapy with Ra-223 needs to be further studied (116).
Another radiopharmaceutical with great therapeutic potential, 177Lu-PSMA-617, specifically identifies tumor cells with high expression of PSMA and releases β-particles to destroy tumor cells, was recently evaluated in the just concluded VISION trial (117). Significant benefits in radiology progression-free survival (rPFS) (8.7 vs 3.4 months, HR=0.40) and OS (15.3 vs 11.3 months, HR=0.62) have been reported, and significant improvements were also observed in all secondary endpoints of the study. Because 177Lu-PSMA-617 also has a favorable safety profile, it has been described as a revolutionary precision radiotherapy modality for the treatment of mCRPC. The PSA response rate was superior to that reported for cabazitaxel and docetaxel in other studies (118, 119). The efficacy and safety of 177Lu-PSMA-617 combined with immunotherapy or other drugs have been explored in patients with mCRPC. Considering the low possibility of overlap in toxicity of radiotherapy combined with other therapeutic agents, 177Lu-PSMA-617 combination therapy may provide a relatively safe treatment option for patients with mCRPC.
6.4 Immunotherapy combined with chemotherapy
Chemotherapy, a conventional treatment for cancer patients, is widely used in the treatment of various malignant diseases. Docetaxel and cabazitaxel have been successively approved for the treatment of patients with mCRPC and have been shown to prolong patient survival and control disease progression. Some studies have shown that chemotherapy-induced tumor cell destruction may enhance the development of specific immune responses (120). A study evaluating pembrolizumab in combination with docetaxel for mCRPC reported the efficacy of combination therapy in patients with mCRPC previously treated with enzalutamide or abiraterone. The PSA response rate was 27% and ORR and DCR were 23% and 52%, respectively. The median OS of combination therapy was 20.2 months, which was significantly prolonged compared to the median OS of 9.5 months in the PD-L1 positive cohort in KEYNOTE-199. KEYNOTE-365 showed initial success with PD-L1 antibodies in combination with chemotherapy. However, the patients included in the study were previously chemotherapy naïve patients. All KEYNOTE-199 patients were treated with docetaxel chemotherapy prior to treatment with PD-L1 antibodies. Nonetheless, we cannot define the specific impact of chemotherapy on the benefit of combination therapy. The ongoing KEYNOTE-921 trial includes patients with mCRPC after chemotherapy and will provide further evidence to support this combination strategy (121).
6.5 Immunotherapy combined with PARP inhibitors
PARP inhibitors have recently become one of the most popular drugs in the mCRPC therapeutic area, and is represented by olaparib and rucaparib. PARP plays an important role in DNA damage repair in vivo, and PARP1 and PARP2 mediate DNA damage repair through base excision. The restoration of single-stranded DNA (ssDNA) damage can be blocked by PARP inhibitors. Homologous recombination repair proteins can compensate for the above by repairing broken double-stranded DNA. However, under the homologous recombination repair gene defect (HRD), this compensatory pathway is blocked. PARP inhibitors and HRD cause a synthetic lethality of tumor cells, generating tumor neoantigens that increase immunogenicity and improve immune responsiveness in the tumor microenvironment (122). The safety and significant therapeutic effects of olaparib and rucaparib monotherapy in patients with mCRPC have been reported in several studies (123, 124). In the TOPARP-A trial, the ORR to treatment was 32%, with a response rate of 88% in patients with DNA repair gene mutations, and other studies have confirmed that patients with genetic defects such as BRCA1, BRCA2, ATM, FANC, and CHEK2 have higher sensitivity to PARP inhibitors (125). PARP inhibitors have been shown to have synergistic effects with PD-1/PD-L1 or CTLA-4 blockade (126, 127). A recent study of rucaparib in combination with nivolumab for mCRPC reported its results: regardless of previous chemotherapy (128), the CheckMate 9KD study showed significantly improved ORR and PSA response rates with combination therapy in the HRD+ cohort, particularly in patients with BRAC1/2 mutations; in terms of OS and rPFS, the median OS for the A2 cohort without chemotherapy was 20.2 months (95% CI 14.1–22.8 months) and the median rPFS was 8.1 months (95% CI 5.6–10.9 months). Regarding safety, common TRAEs observed following combination therapy were nausea, fatigue, anemia, and loss of appetite, with G3-G4 TRAEs occurring in half of the patients in both cohorts, and neutropenia warranting focus during treatment. In general, rucaparib combined with nivolumab did not appear to show additional benefits in unselected mCRPC patients, which is consistent with the findings of the previous KEYLYNK-010 trial of olaparib combined with pembrolizumab. It is also encouraging that a significant response to combination therapy was observed in the subgroup of patients with BRAC1 and BRAC2 mutations, but the failure to translate into a survival benefit is difficult to explain and will require further evidence. Many studies have been conducted to screen and identify new, highly effective therapeutic predictive factors for mCRPC patients (129). Continued advances in next-generation exon sequencing technology and liquid biopsy technology will contribute to the precise treatment of mCRPC patients and will provide more significant benefits to patient.
6.6 Immunotherapy combined tyrosine kinase inhibitors (TKIs)
TKIs represented by Cabozantinib and Masitinib belong to the class of small-molecule inhibitors with RARP inhibitors, and both drugs have shown antitumor activity in previous studies. Cabozantinib is a mesenchymal-epithelial transition factor (c-MET) and vascular endothelial factor receptor 2 (VEGFR2) inhibitor that has been approved for the treatment of patients with advanced renal cell carcinoma. In a phase 2 study, cabozantinib significantly prolonged PFS in patients with CRPC (130). However, in the COMET-1 study, mCRPC patients after chemotherapy failed to show an OS benefit (131). Studies have shown that Cabozantinib has immunomodulatory effects and may be synergistic with other immunotherapy combinations (132, 133). The COSMIC 021 trial evaluated the safety and clinical benefit of Cabozantinib in combination with atezolizumab in patients with mCRPC. The study found that the combination regimen had better PSA response rate and DCR than either drug monotherapy. In terms of safety, 95% of patients experienced TRAEs at any grade and 55% of patients experienced G3-G4. The most common G3-G4 AEs were pulmonary embolism, diarrhea, fatigue, and hypertension. The safety profile of cabozantinib combined with atezolizumab was generally consistent with that of the individual agents, but the incidence of pulmonary embolism is higher than that of monotherapy (134). Elderly age and concurrent use of ADT are possible causes of pulmonary embolism. Due to the differences in patient groups included in different studies, it is difficult to compare the specific benefits of combination therapy at present, and future evidence support from other studies is needed.
7 Limitations and future prospects
There are still many obstacles and challenges in prostate cancer immunotherapy, such as the balance between efficacy and toxicity of immunotherapy, the timing of sequential administration, the requirement of individualized dosing regimen for prostate cancer due to tumor heterogeneity, the lack of appropriate biomarkers for efficacy evaluation, and the insufficient understanding of the mechanism of drug resistance. These issues need to be focused on in the future. Due to the extensive differences between the studies of immunotherapy, there is a lack of direct evidence to support the comparison of the treatment effects of different regimens, and more large-scale controlled trials are needed in the future. Immunotherapy of prostate cancer is a promising treatment. With the deepening of research, new tumor-specific antigens have been discovered, which provides more potential targets for immunotherapy. The continuous progress of high-throughput sequencing technology and liquid biopsy technology has promoted the identification of tumor heterogeneity of prostate cancer and promoted the precision treatment of prostate cancer patients. The continuous exploration of drug combination is helpful to the study of drug interaction mechanism. The development of imaging technology represented by PSMA-PET/CT provides a powerful aid in disease diagnosis and efficacy evaluation.
8 Conclusion
Over the past decade, as immunotherapy for solid tumors continues to be explored, our understanding of immunotherapy and immunomodulation of solid tumors, including prostate cancer, has also improved, and a variety of immunotherapeutic agents, including tumor vaccines and immune checkpoint inhibitors, have achieved exciting results in clinical trials for advanced prostate cancer. Although most current trials on immunotherapy for prostate cancer have focused on patients with mCRPC, there is reason to believe that immunotherapy may bring earlier clinical benefits to prostate cancer patients as immunotherapy continues to improve and mature. In this review, we summarize the experience and lessons learnt from recent immunotherapy studies and update the theoretical basis and regulatory mechanisms underlying immunotherapy for prostate cancer, helping to understand the latest progress in immunotherapy for prostate cancer. As more and more clinical trials are conducted, these will provide strong evidence to support and compare the efficacy of immunotherapy for prostate cancer, providing a valuable reference that will allow more patients with prostate cancer to choose their treatment regimen and prolong survival and also improve the quality of patient survival.
Author contributions
HL and YL wrote the first draft of the manuscript. YL, JG, MD, and HL wrote sections of the manuscript. XZ and LH polished the language and searched the literature. All authors contributed to the article and approved the submitted version.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
1. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin (2021) 71(3):209–49. doi: 10.3322/caac.21660
2. Foreman KJ, Marquez N, Dolgert A, Fukutaki K, Fullman N, McGaughey M, et al. Forecasting life expectancy, years of life lost, and all-cause and cause-specific mortality for 250 causes of death: reference and alternative scenarios for 2016-40 for 195 countries and territories. Lancet. (2018) 392(10159):2052–90. doi: 10.1016/S0140-6736(18)31694-5
3. Mottet N, van den Bergh RCN, Briers E, Van den Broeck T, Cumberbatch MG, De Santis M, et al. EAU-EANM-ESTRO-ESUR-SIOG guidelines on prostate cancer-2020 update. part 1: Screening, diagnosis, and local treatment with curative intent. Eur Urol (2021) 79(2):243–62. doi: 10.1016/j.eururo.2020.09.042
4. Schaeffer E, Srinivas S, Antonarakis ES, Armstrong AJ, Bekelman JE, Cheng H, et al. NCCN guidelines insights: Prostate cancer, version 1. 2021. J Natl Compr Canc Netw (2021) 19(2):134–43. doi: 10.6004/jnccn.2021.0008
5. Eastham JA, Auffenberg GB, Barocas DA, Chou R, Crispino T, Davis JW, et al. Clinically localized prostate cancer: AUA/ASTRO guideline, part II: Principles of active surveillance, principles of surgery, and follow-up. J Urol. (2022) 208(1):19–25. doi: 10.1097/JU.0000000000002758
6. Eastham JA, Auffenberg GB, Barocas DA, Chou R, Crispino T, Davis JW, et al. Clinically localized prostate cancer: AUA/ASTRO guideline. part III: Principles of radiation and future directions. J Urol (2022) 208(1):26–33. doi: 10.1097/JU.0000000000002759
7. Sandhu S, Moore CM, Chiong E, Beltran H, Bristow RG, Williams SG. Prostate cancer. Lancet. (2021) 398(10305):1075–90. doi: 10.1016/S0140-6736(21)00950-8
8. Powers E, Karachaliou GS, Kao C, Harrison MR, Hoimes CJ, George DJ, et al. Novel therapies are changing treatment paradigms in metastatic prostate cancer. J Hematol Oncol (2020) 13(1):144. doi: 10.1186/s13045-020-00978-z
9. Siegel RL, Miller KD, Fuchs HE, Jemal A. Cancer statistics, 2021. CA Cancer J Clin (2021) 71(1):7–33. doi: 10.3322/caac.21654
10. Hofman MS, Lawrentschuk N, Francis RJ, Tang C, Vela I, Thomas P, et al. Prostate-specific membrane antigen PET-CT in patients with high-risk prostate cancer before curative-intent surgery or radiotherapy (proPSMA): a prospective, randomised, multicentre study. Lancet. (2020) 395(10231):1208–16. doi: 10.1016/S0140-6736(20)30314-7
11. Wang Y, Galante JR, Haroon A, Wan S, Afaq A, Payne H, et al. The future of PSMA PET and WB MRI as next-generation imaging tools in prostate cancer. Nat Rev Urol. (2022) 19(8):475–93. doi: 10.1038/s41585-022-00618-w
12. Shen K, Liu B, Zhou X, Ji Y, Chen L, Wang Q, et al. The evolving role of 18F-FDG PET/CT in diagnosis and prognosis prediction in progressive prostate cancer. Front Oncol (2021) 11:683793. doi: 10.3389/fonc.2021.683793
13. Swami U, McFarland TR, Nussenzveig R, Agarwal N. Advanced prostate cancer: Treatment advances and future directions. Trends Cancer. (2020) 6(8):702–15. doi: 10.1016/j.trecan.2020.04.010
14. Buck SAJ, Koolen SLW, Mathijssen RHJ, de Wit R, van Soest RJ. Cross-resistance and drug sequence in prostate cancer. Drug Resist Updat. (2021) 56:100761. doi: 10.1016/j.drup.2021.100761
15. Cha H-R, Lee JH, Ponnazhagan S. Revisiting immunotherapy: A focus on prostate cancer. Cancer Res (2020) 80(8):1615–23. doi: 10.1158/0008-5472.CAN-19-2948
16. Hiam-Galvez KJ, Allen BM, Spitzer MH. Systemic immunity in cancer. Nat Rev Cancer. (2021) 21(6):345–59. doi: 10.1038/s41568-021-00347-z
17. Melero I, Castanon E, Alvarez M, Champiat S, Marabelle A. Intratumoural administration and tumour tissue targeting of cancer immunotherapies. Nat Rev Clin Oncol (2021) 18(9):558–76. doi: 10.1038/s41571-021-00507-y
18. Gu Z, Thomas G, Yamashiro J, Shintaku IP, Dorey F, Raitano A, et al. Prostate stem cell antigen (PSCA) expression increases with high gleason score, advanced stage and bone metastasis in prostate cancer. Oncogene. (2000) 19(10):1288–96. doi: 10.1038/sj.onc.1203426
19. Bostwick DG, Pacelli A, Blute M, Roche P, Murphy GP. Prostate specific membrane antigen expression in prostatic intraepithelial neoplasia and adenocarcinoma: a study of 184 cases. Cancer. (1998) 82(11):2256–61. doi: 10.1002/(sici)1097-0142(19980601)82:11<2256::aid-cncr22>3.0.co;2-s
20. Hupe MC, Philippi C, Roth D, Kümpers C, Ribbat-Idel J, Becker F, et al. Expression of prostate-specific membrane antigen (PSMA) on biopsies is an independent risk stratifier of prostate cancer patients at time of initial diagnosis. Front Oncol (2018) 8:623. doi: 10.3389/fonc.2018.00623
21. Bou-Dargham MJ, Sha L, Sang Q-XA, Zhang J. Immune landscape of human prostate cancer: immune evasion mechanisms and biomarkers for personalized immunotherapy. BMC Cancer. (2020) 20(1):572. doi: 10.1186/s12885-020-07058-y
22. DePeaux K, Delgoffe GM. Metabolic barriers to cancer immunotherapy. Nat Rev Immunol (2021) 21(12):785–97. doi: 10.1038/s41577-021-00541-y
23. Briukhovetska D, Dörr J, Endres S, Libby P, Dinarello CA, Kobold S. Interleukins in cancer: from biology to therapy. Nat Rev Cancer. (2021) 21(8):481–99. doi: 10.1038/s41568-021-00363-z
24. Higano CS, Small EJ, Schellhammer P, Yasothan U, Gubernick S, Kirkpatrick P, et al. Sipuleucel-T. Nat Rev Drug Discovery (2010) 9(7):513–4. doi: 10.1038/nrd3220
25. Kantoff PW, Higano CS, Shore ND, Berger ER, Small EJ, Penson DF, et al. Sipuleucel-T immunotherapy for castration-resistant prostate cancer. N Engl J Med (2010) 363(5):411–22. doi: 10.1056/NEJMoa1001294
26. Small EJ, Schellhammer PF, Higano CS, Redfern CH, Nemunaitis JJ, Valone FH, et al. Placebo-controlled phase III trial of immunologic therapy with sipuleucel-T (APC8015) in patients with metastatic, asymptomatic hormone refractory prostate cancer. J Clin Oncol (2006) 24(19):3089–94. doi: 10.1200/JCO.2005.04.5252
27. Higano CS, Armstrong AJ, Sartor AO, Vogelzang NJ, Kantoff PW, McLeod DG, et al. Real-world outcomes of sipuleucel-T treatment in PROCEED, a prospective registry of men with metastatic castration-resistant prostate cancer. Cancer. (2019) 125(23):4172–80. doi: 10.1002/cncr.32445
28. Stein WD, Gulley JL, Schlom J, Madan RA, Dahut W, Figg WD, et al. Tumor regression and growth rates determined in five intramural NCI prostate cancer trials: the growth rate constant as an indicator of therapeutic efficacy. Clin Cancer Res (2011) 17(4):907–17. doi: 10.1158/1078-0432.CCR-10-1762
29. Kantoff PW, Schuetz TJ, Blumenstein BA, Glode LM, Bilhartz DL, Wyand M, et al. Overall survival analysis of a phase II randomized controlled trial of a poxviral-based PSA-targeted immunotherapy in metastatic castration-resistant prostate cancer. J Clin Oncol (2010) 28(7):1099–105. doi: 10.1200/JCO.2009.25.0597
30. Kantoff PW, Gulley JL, Pico-Navarro C. Revised overall survival analysis of a Phase II, Randomized, double-blind, controlled study of PROSTVAC in men with metastatic castration-resistant prostate cancer. J Clin Oncol (2017) 35(1):124–5. doi: 10.1200/JCO.2016.69.7748
31. Gulley JL, Borre M, Vogelzang NJ, Ng S, Agarwal N, Parker CC, et al. Phase III trial of PROSTVAC in asymptomatic or minimally symptomatic metastatic castration-resistant prostate cancer. J Clin Oncol (2019) 37(13):1051–61. doi: 10.1200/JCO.18.02031
32. Abdul Sater H, Marté JL, Donahue RN, Walter-Rodriguez B, Heery CR, Steinberg SM, et al. Neoadjuvant PROSTVAC prior to radical prostatectomy enhances T-cell infiltration into the tumor immune microenvironment in men with prostate cancer. J Immunother Cancer (2020) 8(1):e000655. doi: 10.1136/jitc-2020-000655
33. Madan RA, Karzai F, Donahue RN, Al-Harthy M, Bilusic M, Rosner II, et al. Clinical and immunologic impact of short-course enzalutamide alone and with immunotherapy in non-metastatic castration sensitive prostate cancer. J Immunother Cancer (2021) 9(3):e001556. doi: 10.1136/jitc-2020-001556
34. Podrazil M, Horvath R, Becht E, Rozkova D, Bilkova P, Sochorova K, et al. Phase I/II clinical trial of dendritic-cell based immunotherapy (DCVAC/PCa) combined with chemotherapy in patients with metastatic, castration-resistant prostate cancer. Oncotarget. (2015) 6(20):18192–205. doi: 10.18632/oncotarget.4145
35. Fucikova J, Podrazil M, Jarolim L, Bilkova P, Hensler M, Becht E, et al. Phase I/II trial of dendritic cell-based active cellular immunotherapy with DCVAC/PCa in patients with rising PSA after primary prostatectomy or salvage radiotherapy for the treatment of prostate cancer. Cancer Immunol Immunother (2018) 67(1):89–100. doi: 10.1007/s00262-017-2068-x
36. Vogelzang NJ, Beer TM, Gerritsen W, Oudard S, Wiechno P, Kukielka-Budny B, et al. Efficacy and safety of autologous dendritic cell-based immunotherapy, docetaxel, and prednisone vs placebo in patients with metastatic castration-resistant prostate cancer: The VIABLE phase 3 randomized clinical trial. JAMA Oncol (2022) 8(4):546–52. doi: 10.1001/jamaoncol.2021.7298
37. McNeel DG, Becker JT, Eickhoff JC, Johnson LE, Bradley E, Pohlkamp I, et al. Real-time immune monitoring to guide plasmid DNA vaccination schedule targeting prostatic acid phosphatase in patients with castration-resistant prostate cancer. Clin Cancer Res (2014) 20(14):3692–704. doi: 10.1158/1078-0432.CCR-14-0169
38. McNeel DG, Eickhoff JC, Johnson LE, Roth AR, Perk TG, Fong L, et al. Phase II trial of a DNA vaccine encoding prostatic acid phosphatase (pTVG-HP [MVI-816]) in patients with progressive, nonmetastatic, castration-sensitive prostate cancer. J Clin Oncol (2019) 37(36):3507–17. doi: 10.1200/JCO.19.01701
39. McNeel DG, Eickhoff JC, Wargowski E, Johnson LE, Kyriakopoulos CE, Emamekhoo H, et al. Phase 2 trial of T-cell activation using MVI-816 and pembrolizumab in patients with metastatic, castration-resistant prostate cancer (mCRPC). J Immunother Cancer (2022) 10(3):e004198. doi: 10.1136/jitc-2021-004198
40. Kyriakopoulos CE, Eickhoff JC, Ferrari AC, Schweizer MT, Wargowski E, Olson BM, et al. Multicenter phase I trial of a DNA vaccine encoding the androgen receptor ligand-binding domain (pTVG-AR, MVI-118) in patients with metastatic prostate cancer. Clin Cancer Res (2020) 26(19):5162–71. doi: 10.1158/1078-0432.CCR-20-0945
41. Elia AR, Caputo S, Bellone M. Immune checkpoint-mediated interactions between cancer and immune cells in prostate adenocarcinoma and melanoma. Front Immunol (2018) 9:1786. doi: 10.3389/fimmu.2018.01786
42. Jiao S, Subudhi SK, Aparicio A, Ge Z, Guan B, Miura Y, et al. Differences in tumor microenvironment dictate T helper lineage polarization and response to immune checkpoint therapy. Cell (2019) 179(5):1177–90.e13. doi: 10.1016/j.cell.2019.10.029
43. Fuchs CS, Doi T, Jang RW, Muro K, Satoh T, Machado M, et al. Safety and efficacy of pembrolizumab monotherapy in patients with previously treated advanced gastric and gastroesophageal junction cancer: Phase 2 clinical KEYNOTE-059 trial. JAMA Oncol (2018) 4(5):e180013. doi: 10.1001/jamaoncol.2018.0013
44. Hellmann MD, Rizvi NA, Goldman JW, Gettinger SN, Borghaei H, Brahmer JR, et al. Nivolumab plus ipilimumab as first-line treatment for advanced non-small-cell lung cancer (CheckMate 012): results of an open-label, phase 1, multicohort study. Lancet Oncol (2017) 18(1):31–41. doi: 10.1016/S1470-2045(16)30624-6
45. Patel MR, Ellerton J, Infante JR, Agrawal M, Gordon M, Aljumaily R, et al. Avelumab in metastatic urothelial carcinoma after platinum failure (JAVELIN solid tumor): pooled results from two expansion cohorts of an open-label, phase 1 trial. Lancet Oncol (2018) 19(1):51–64. doi: 10.1016/S1470-2045(17)30900-2
46. Nicholson LT, Fong L. Immune checkpoint inhibition in prostate cancer. Trends Cancer. (2020) 6(3):174–7. doi: 10.1016/j.trecan.2020.01.003
47. Claps M, Mennitto A, Guadalupi V, Sepe P, Stellato M, Zattarin E, et al. Immune-checkpoint inhibitors and metastatic prostate cancer therapy: Learning by making mistakes. Cancer Treat Rev (2020) 88:102057. doi: 10.1016/j.ctrv.2020.102057
48. Cameron F, Whiteside G, Perry C. Ipilimumab: first global approval. Drugs. (2011) 71(8):1093–104. doi: 10.2165/11594010-000000000-00000
49. Beer TM, Kwon ED, Drake CG, Fizazi K, Logothetis C, Gravis G, et al. Randomized, double-blind, phase III trial of ipilimumab versus placebo in asymptomatic or minimally symptomatic patients with metastatic chemotherapy-naive castration-resistant prostate cancer. J Clin Oncol (2017) 35(1):40–7. doi: 10.1200/JCO.2016.69.1584
50. Kwon ED, Drake CG, Scher HI, Fizazi K, Bossi A, van den Eertwegh AJM, et al. Ipilimumab versus placebo after radiotherapy in patients with metastatic castration-resistant prostate cancer that had progressed after docetaxel chemotherapy (CA184-043): a multicentre, randomised, double-blind, phase 3 trial. Lancet Oncol (2014) 15(7):700–12. doi: 10.1016/S1470-2045(14)70189-5
51. Subudhi SK, Vence L, Zhao H, Blando J, Yadav SS, Xiong Q, et al. Neoantigen responses, immune correlates, and favorable outcomes after ipilimumab treatment of patients with prostate cancer. Sci Transl Med (2020) 12(537):eaaz3577. doi: 10.1126/scitranslmed.aaz3577
52. Dong H, Strome SE, Salomao DR, Tamura H, Hirano F, Flies DB, et al. Tumor-associated B7-H1 promotes T-cell apoptosis: a potential mechanism of immune evasion. Nat Med (2002) 8(8):793–800. doi: 10.1038/nm730
53. Hodi FS, O'Day SJ, McDermott DF, Weber RW, Sosman JA, Haanen JB, et al. Improved survival with ipilimumab in patients with metastatic melanoma. N Engl J Med (2010) 363(8):711–23. doi: 10.1056/NEJMoa1003466
54. Larkin J, Chiarion-Sileni V, Gonzalez R, Grob JJ, Cowey CL, Lao CD, et al. Combined nivolumab and ipilimumab or monotherapy in untreated melanoma. N Engl J Med (2015) 373(1):23–34. doi: 10.1056/NEJMoa1504030
55. Wolchok JD, Chiarion-Sileni V, Gonzalez R, Rutkowski P, Grob J-J, Cowey CL, et al. Overall survival with combined nivolumab and ipilimumab in advanced melanoma. N Engl J Med (2017) 377(14):1345–56. doi: 10.1056/NEJMoa1709684
56. Topalian SL, Hodi FS, Brahmer JR, Gettinger SN, Smith DC, McDermott DF, et al. Safety, activity, and immune correlates of anti-PD-1 antibody in cancer. N Engl J Med (2012) 366(26):2443–54. doi: 10.1056/NEJMoa1200690
57. Hansen AR, Massard C, Ott PA, Haas NB, Lopez JS, Ejadi S, et al. Pembrolizumab for advanced prostate adenocarcinoma: findings of the KEYNOTE-028 study. Ann Oncol (2018) 29(8):1807–13. doi: 10.1093/annonc/mdy232
58. Antonarakis ES, Piulats JM, Gross-Goupil M, Goh J, Ojamaa K, Hoimes CJ, et al. Pembrolizumab for treatment-refractory metastatic castration-resistant prostate cancer: Multicohort, open-label phase II KEYNOTE-199 study. J Clin Oncol (2020) 38(5):395–405. doi: 10.1200/JCO.19.01638
59. Graf RP, Fisher V, Weberpals J, Gjoerup O, Tierno MB, Huang RSP, et al. Comparative effectiveness of immune checkpoint inhibitors vs chemotherapy by tumor mutational burden in metastatic castration-resistant prostate cancer. JAMA Netw Open (2022) 5(3):e225394. doi: 10.1001/jamanetworkopen.2022.5394
60. Gao J, Ward JF, Pettaway CA, Shi LZ, Subudhi SK, Vence LM, et al. VISTA is an inhibitory immune checkpoint that is increased after ipilimumab therapy in patients with prostate cancer. Nat Med (2017) 23(5):551–5. doi: 10.1038/nm.4308
61. Sharma P, Pachynski RK, Narayan V, Fléchon A, Gravis G, Galsky MD, et al. Nivolumab plus ipilimumab for metastatic castration-resistant prostate cancer: Preliminary analysis of patients in the CheckMate 650 trial. Cancer Cell (2020) 38(4):489–99.e3. doi: 10.1016/j.ccell.2020.08.007
62. Vestergaard LK, Oliveira DNP, Høgdall CK, Høgdall EV. Next generation sequencing technology in the clinic and its challenges. Cancers (Basel) (2021) 13(8):1751. doi: 10.3390/cancers13081751
63. Yu W, Hurley J, Roberts D, Chakrabortty SK, Enderle D, Noerholm M, et al. Exosome-based liquid biopsies in cancer: opportunities and challenges. Ann Oncol (2021) 32(4):466–77. doi: 10.1016/j.annonc.2021.01.074
64. Graff JN, Alumkal JJ, Drake CG, Thomas GV, Redmond WL, Farhad M, et al. Early evidence of anti-PD-1 activity in enzalutamide-resistant prostate cancer. Oncotarget. (2016) 7(33):52810–7. doi: 10.18632/oncotarget.10547
65. Schweizer MT, Cheng HH, Tretiakova MS, Vakar-Lopez F, Klemfuss N, Konnick EQ, et al. Mismatch repair deficiency may be common in ductal adenocarcinoma of the prostate. Oncotarget. (2016) 7(50):82504–10. doi: 10.18632/oncotarget.12697
66. McGrail DJ, Federico L, Li Y, Dai H, Lu Y, Mills GB, et al. Multi-omics analysis reveals neoantigen-independent immune cell infiltration in copy-number driven cancers. Nat Commun (2018) 9(1):1317. doi: 10.1038/s41467-018-03730-x
67. McGrail DJ, Pilié PG, Rashid NU, Voorwerk L, Slagter M, Kok M, et al. High tumor mutation burden fails to predict immune checkpoint blockade response across all cancer types. Ann Oncol (2021) 32(5):661–72. doi: 10.1016/j.annonc.2021.02.006
68. Britten CM, Shalabi A, Hoos A. Industrializing engineered autologous T cells as medicines for solid tumours. Nat Rev Drug Discovery (2021) 20(6):476–88. doi: 10.1038/s41573-021-00175-8
69. Daher M, Rezvani K. Outlook for new CAR-based therapies with a focus on CAR NK cells: What lies beyond CAR-engineered T cells in the race against cancer. Cancer Discovery (2021) 11(1):45–58. doi: 10.1158/2159-8290.CD-20-0556
70. Chong EA, Ruella M, Schuster SJ. Five-year outcomes for refractory b-cell lymphomas with CAR T-cell therapy. N Engl J Med (2021) 384(7):673–4. doi: 10.1056/NEJMc2030164
71. Park JH, Rivière I, Gonen M, Wang X, Sénéchal B, Curran KJ, et al. Long-term follow-up of CD19 CAR therapy in acute lymphoblastic leukemia. N Engl J Med (2018) 378(5):449–59. doi: 10.1056/NEJMoa1709919
72. Maude SL, Laetsch TW, Buechner J, Rives S, Boyer M, Bittencourt H, et al. Tisagenlecleucel in children and young adults with b-cell lymphoblastic leukemia. N Engl J Med (2018) 378(5):439–48. doi: 10.1056/NEJMoa1709866
73. Mullard A. FDA Approves fourth CAR-T cell therapy. Nat Rev Drug Discovery (2021) 20(3):166. doi: 10.1038/d41573-021-00031-9
74. June CH, Sadelain M. Chimeric antigen receptor therapy. N Engl J Med (2018) 379(1):64–73. doi: 10.1056/NEJMra1706169
75. Schepisi G, Cursano MC, Casadei C, Menna C, Altavilla A, Lolli C, et al. CAR-T cell therapy: a potential new strategy against prostate cancer. J Immunother Cancer. (2019) 7(1):258. doi: 10.1186/s40425-019-0741-7
76. Fujiwara K, Tsunei A, Kusabuka H, Ogaki E, Tachibana M, Okada N. Hinge and transmembrane domains of chimeric antigen receptor regulate receptor expression and signaling threshold. Cells (2020) 9(5):1182. doi: 10.3390/cells9051182
77. Majzner RG, Ramakrishna S, Yeom KW, Patel S, Chinnasamy H, Schultz LM, et al. GD2-CAR T cell therapy for H3K27M-mutated diffuse midline gliomas. Nature. (2022) 603(7903):934–41. doi: 10.1038/s41586-022-04489-4
78. Hou AJ, Chen LC, Chen YY. Navigating CAR-T cells through the solid-tumour microenvironment. Nat Rev Drug Discovery (2021) 20(7):531–50. doi: 10.1038/s41573-021-00189-2
79. June CH, O'Connor RS, Kawalekar OU, Ghassemi S, Milone MC. CAR T cell immunotherapy for human cancer. Science. (2018) 359(6382):1361–5. doi: 10.1126/science.aar6711
80. Narayan V, Barber-Rotenberg JS, Jung I-Y, Lacey SF, Rech AJ, Davis MM, et al. PSMA-targeting TGFβ-insensitive armored CAR t cells in metastatic castration-resistant prostate cancer: a phase 1 trial. Nat Med (2022) 28(4):724–34. doi: 10.1038/s41591-022-01726-1
81. Tschernia NP, Norberg SM, Gulley JL. CAR T cells reach clinical milestone in prostate cancer. Nat Med (2022) 28(4):635–6. doi: 10.1038/s41591-022-01742-1
82. Dorff TB, Narayan V, Forman SJ, Zang PD, Fraietta JA, June CH, et al. Novel redirected T-cell immunotherapies for advanced prostate cancer. Clin Cancer Res (2022) 28(4):576–84. doi: 10.1158/1078-0432.CCR-21-1483
83. Wolf P, Alzubi J, Gratzke C, Cathomen T. The potential of CAR T cell therapy for prostate cancer. Nat Rev Urol. (2021) 18(9):556–71. doi: 10.1038/s41585-021-00488-8
84. Zhang X, Sun S, Miao Y, Yuan Y, Zhao W, Li H, et al. Docetaxel enhances the therapeutic efficacy of PSMA-specific CAR-T cells against prostate cancer models by suppressing MDSCs. J Cancer Res Clin Oncol (2022) 148(12):3511–20. doi: 10.1007/s00432-022-04248-y
85. Kamat NV, Yu EY, Lee JK. BiTE-ing into prostate cancer with bispecific T-cell engagers. Clin Cancer Res (2021) 27(10):2675–7. doi: 10.1158/1078-0432.CCR-21-0355
86. Goebeler M-E, Bargou RC. T Cell-engaging therapies - BiTEs and beyond. Nat Rev Clin Oncol (2020) 17(7):418–34. doi: 10.1038/s41571-020-0347-5
87. Deegen P, Thomas O, Nolan-Stevaux O, Li S, Wahl J, Bogner P, et al. The PSMA-targeting half-life extended BiTE therapy AMG 160 has potent antitumor activity in preclinical models of metastatic castration-resistant prostate cancer. Clin Cancer Res (2021) 27(10):2928–37. doi: 10.1158/1078-0432.CCR-20-3725
88. Hummel H-D, Kufer P, Grüllich C, Seggewiss-Bernhardt R, Deschler-Baier B, Chatterjee M, et al. Pasotuxizumab, a BiTE® immune therapy for castration-resistant prostate cancer: Phase I, dose-escalation study findings. Immunotherapy. (2021) 13(2):125–41. doi: 10.2217/imt-2020-0256
89. Slaney CY, Wang P, Darcy PK, Kershaw MH. CARs versus BiTEs: A comparison between T cell-redirection strategies for cancer treatment. Cancer Discovery (2018) 8(8):924–34. doi: 10.1158/2159-8290.CD-18-0297
90. Hegde PS, Chen DS. Top 10 challenges in cancer immunotherapy. Immunity. (2020) 52(1):17–35. doi: 10.1016/j.immuni.2019.12.011
91. Heitmann JS, Pfluegler M, Jung G, Salih HR. Bispecific antibodies in prostate cancer therapy: Current status and perspectives. Cancers (Basel) (2021) 13(3):549. doi: 10.3390/cancers13030549
92. Braig F, Brandt A, Goebeler M, Tony H-P, Kurze A-K, Nollau P, et al. Resistance to anti-CD19/CD3 BiTE in acute lymphoblastic leukemia may be mediated by disrupted CD19 membrane trafficking. Blood. (2017) 129(1):100–4. doi: 10.1182/blood-2016-05-718395
93. Giffin MJ, Cooke K, Lobenhofer EK, Estrada J, Zhan J, Deegen P, et al. AMG 757, a half-life extended, DLL3-targeted bispecific T-cell engager, shows high potency and sensitivity in preclinical models of small-cell lung cancer. Clin Cancer Res (2021) 27(5):1526–37. doi: 10.1158/1078-0432.CCR-20-2845
94. Yamamoto K, Trad A, Baumgart A, Hüske L, Lorenzen I, Chalaris A, et al. A novel bispecific single-chain antibody for ADAM17 and CD3 induces T-cell-mediated lysis of prostate cancer cells. Biochem J (2012) 445(1):135–44. doi: 10.1042/BJ20120433
95. Einsele H, Borghaei H, Orlowski RZ, Subklewe M, Roboz GJ, Zugmaier G, et al. The BiTE (bispecific T-cell engager) platform: Development and future potential of a targeted immuno-oncology therapy across tumor types. Cancer. (2020) 126(14):3192–201. doi: 10.1002/cncr.32909
96. Sinha M, Zhang L, Subudhi S, Chen B, Marquez J, Liu EV, et al. Pre-existing immune status associated with response to combination of sipuleucel-T and ipilimumab in patients with metastatic castration-resistant prostate cancer. J Immunother Cancer (2021) 9(5):e002254. doi: 10.1136/jitc-2020-002254
97. Slovin SF, Higano CS, Hamid O, Tejwani S, Harzstark A, Alumkal JJ, et al. Ipilimumab alone or in combination with radiotherapy in metastatic castration-resistant prostate cancer: results from an open-label, multicenter phase I/II study. Ann Oncol (2013) 24(7):1813–21. doi: 10.1093/annonc/mdt107
98. Wargowski E, Johnson LE, Eickhoff JC, Delmastro L, Staab MJ, Liu G, et al. Prime-boost vaccination targeting prostatic acid phosphatase (PAP) in patients with metastatic castration-resistant prostate cancer (mCRPC) using sipuleucel-T and a DNA vaccine. J Immunother Cancer. (2018) 6(1):21. doi: 10.1186/s40425-018-0333-y
99. Tran C, Ouk S, Clegg NJ, Chen Y, Watson PA, Arora V, et al. Development of a second-generation antiandrogen for treatment of advanced prostate cancer. Science. (2009) 324(5928):787–90. doi: 10.1126/science.1168175
100. Fizazi K, Foulon S, Carles J, Roubaud G, McDermott R, Fléchon A, et al. Abiraterone plus prednisone added to androgen deprivation therapy and docetaxel in de novo metastatic castration-sensitive prostate cancer (PEACE-1): a multicentre, open-label, randomised, phase 3 study with a 2 × 2 factorial design. Lancet. (2022) 399(10336):1695–707. doi: 10.1016/S0140-6736(22)00367-1
101. Ben-Batalla I, Vargas-Delgado ME, von Amsberg G, Janning M, Loges S. Influence of androgens on immunity to self and foreign: Effects on immunity and cancer. Front Immunol (2020) 11:1184. doi: 10.3389/fimmu.2020.01184
102. Cioni B, Zaalberg A, van Beijnum JR, Melis MHM, van Burgsteden J, Muraro MJ, et al. Androgen receptor signalling in macrophages promotes TREM-1-mediated prostate cancer cell line migration and invasion. Nat Commun (2020) 11(1):4498. doi: 10.1038/s41467-020-18313-y
103. Radojevic K, Arsenovic-Ranin N, Kosec D, Pesic V, Pilipovic I, Perisic M, et al. Neonatal castration affects intrathymic kinetics of T-cell differentiation and the spleen T-cell level. J Endocrinol (2007) 192(3):669–82. doi: 10.1677/joe.1.07019
104. Pu Y, Xu M, Liang Y, Yang K, Guo Y, Yang X, et al. Androgen receptor antagonists compromise T cell response against prostate cancer leading to early tumor relapse. Sci Transl Med (2016) 8(333):333ra47. doi: 10.1126/scitranslmed.aad5659
105. Guan X, Polesso F, Wang C, Sehrawat A, Hawkins RM, Murray SE, et al. Androgen receptor activity in T cells limits checkpoint blockade efficacy. Nature. (2022) 606(7915):791–6. doi: 10.1038/s41586-022-04522-6
106. Madan RA, Gulley JL, Schlom J, Steinberg SM, Liewehr DJ, Dahut WL, et al. Analysis of overall survival in patients with nonmetastatic castration-resistant prostate cancer treated with vaccine, nilutamide, and combination therapy. Clin Cancer Res (2008) 14(14):4526–31. doi: 10.1158/1078-0432.CCR-07-5048
107. Powles T, Yuen KC, Gillessen S, Kadel EE, Rathkopf D, Matsubara N, et al. Atezolizumab with enzalutamide versus enzalutamide alone in metastatic castration-resistant prostate cancer: a randomized phase 3 trial. Nat Med (2022) 28(1):144–53. doi: 10.1038/s41591-021-01600-6
108. Lin L, Kane N, Kobayashi N, Kono EA, Yamashiro JM, Nickols NG, et al. High-dose per fraction radiotherapy induces both antitumor immunity and immunosuppressive responses in prostate tumors. Clin Cancer Res (2021) 27(5):1505–15. doi: 10.1158/1078-0432.CCR-20-2293
109. Parker C, Lewington V, Shore N, Kratochwil C, Levy M, Lindén O, et al. Targeted alpha therapy, an emerging class of cancer agents: A review. JAMA Oncol (2018) 4(12):1765–72. doi: 10.1001/jamaoncol.2018.4044
110. Henriksen G, Breistøl K, Bruland ØS, Fodstad Ø, Larsen RH. Significant antitumor effect from bone-seeking, alpha-particle-emitting (223)Ra demonstrated in an experimental skeletal metastases model. Cancer Res (2002) 62(11):3120–5.
111. FDA Approves radiopharmaceutical for metastatic prostate cancer. Cancer Discovery (2013) 3(7):OF1. doi: 10.1158/2159-8290.CD-NB2013-088
112. Hoskin P, Sartor O, O'Sullivan JM, Johannessen DC, Helle SI, Logue J, et al. Efficacy and safety of radium-223 dichloride in patients with castration-resistant prostate cancer and symptomatic bone metastases, with or without previous docetaxel use: a prespecified subgroup analysis from the randomised, double-blind, phase 3 ALSYMPCA trial. Lancet Oncol (2014) 15(12):1397–406. doi: 10.1016/S1470-2045(14)70474-7
113. Saad F, Carles J, Gillessen S, Heidenreich A, Heinrich D, Gratt J, et al. Radium-223 and concomitant therapies in patients with metastatic castration-resistant prostate cancer: an international, early access, open-label, single-arm phase 3b trial. Lancet Oncol (2016) 17(9):1306–16. doi: 10.1016/S1470-2045(16)30173-5
114. Marshall CH, Fu W, Wang H, Park JC, DeWeese TL, Tran PT, et al. Randomized phase II trial of sipuleucel-T with or without radium-223 in men with bone-metastatic castration-resistant prostate cancer. Clin Cancer Res (2021) 27(6):1623–30. doi: 10.1158/1078-0432.CCR-20-4476
115. Twardowski P, Wong JYC, Pal SK, Maughan BL, Frankel PH, Franklin K, et al. Randomized phase II trial of sipuleucel-T immunotherapy preceded by sensitizing radiation therapy and sipuleucel-T alone in patients with metastatic castrate resistant prostate cancer. Cancer Treat Res Commun (2019) 19:100116. doi: 10.1016/j.ctarc.2018.100116
116. Fong L, Morris MJ, Sartor O, Higano CS, Pagliaro L, Alva A, et al. A phase ib study of atezolizumab with radium-223 dichloride in men with metastatic castration-resistant prostate cancer. Clin Cancer Res (2021) 27(17):4746–56. doi: 10.1158/1078-0432.CCR-21-0063
117. Sartor O, de Bono J, Chi KN, Fizazi K, Herrmann K, Rahbar K, et al. Lutetium-177-PSMA-617 for metastatic castration-resistant prostate cancer. N Engl J Med (2021) 385(12):1091–103. doi: 10.1056/NEJMoa2107322
118. Hofman MS, Emmett L, Sandhu S, Iravani A, Joshua AM, Goh JC, et al. [177Lu]Lu-PSMA-617 versus cabazitaxel in patients with metastatic castration-resistant prostate cancer (TheraP): a randomised, open-label, phase 2 trial. Lancet. (2021) 397(10276):797–804. doi: 10.1016/S0140-6736(21)00237-3
119. Satapathy S, Mittal BR, Sood A, Das CK, Mavuduru RS, Goyal S, et al. 177Lu-PSMA-617 versus docetaxel in chemotherapy-naïve metastatic castration-resistant prostate cancer: a randomized, controlled, phase 2 non-inferiority trial. Eur J Nucl Med Mol Imaging. (2022) 49(5):1754–64. doi: 10.1007/s00259-021-05618-3
120. Heinhuis KM, Ros W, Kok M, Steeghs N, Beijnen JH, Schellens JHM. Enhancing antitumor response by combining immune checkpoint inhibitors with chemotherapy in solid tumors. Ann Oncol (2019) 30(2):219–35. doi: 10.1093/annonc/mdy551
121. Petrylak DP, Ratta R, Gafanov R, Facchini G, Piulats JM, Kramer G, et al. KEYNOTE-921: Phase III study of pembrolizumab plus docetaxel for metastatic castration-resistant prostate cancer. Future Oncol (2021) 17(25):3291–9. doi: 10.2217/fon-2020-1133
122. Stewart RA, Pilié PG, Yap TA. Development of PARP and immune-checkpoint inhibitor combinations. Cancer Res (2018) 78(24):6717–25. doi: 10.1158/0008-5472.CAN-18-2652
123. Mateo J, Carreira S, Sandhu S, Miranda S, Mossop H, Perez-Lopez R, et al. DNA-Repair defects and olaparib in metastatic prostate cancer. N Engl J Med (2015) 373(18):1697–708. doi: 10.1056/NEJMoa1506859
124. de Bono J, Mateo J, Fizazi K, Saad F, Shore N, Sandhu S, et al. Olaparib for metastatic castration-resistant prostate cancer. N Engl J Med (2020) 382(22):2091–102. doi: 10.1056/NEJMoa1911440
125. Stover EH, Konstantinopoulos PA, Matulonis UA, Swisher EM. Biomarkers of response and resistance to DNA repair targeted therapies. Clin Cancer Res (2016) 22(23):5651–60. doi: 10.1158/1078-0432.CCR-16-0247
126. Shen J, Zhao W, Ju Z, Wang L, Peng Y, Labrie M, et al. PARPi triggers the STING-dependent immune response and enhances the therapeutic efficacy of immune checkpoint blockade independent of BRCAness. Cancer Res (2019) 79(2):311–9. doi: 10.1158/0008-5472.CAN-18-1003
127. Higuchi T, Flies DB, Marjon NA, Mantia-Smaldone G, Ronner L, Gimotty PA, et al. CTLA-4 blockade synergizes therapeutically with PARP inhibition in BRCA1-deficient ovarian cancer. Cancer Immunol Res (2015) 3(11):1257–68. doi: 10.1158/2326-6066.CIR-15-0044
128. Fizazi K, Retz M, Petrylak DP, Goh JC, Perez-Gracia J, Lacombe L, et al. Nivolumab plus rucaparib for metastatic castration-resistant prostate cancer: results from the phase 2 CheckMate 9KD trial. J Immunother Cancer (2022) 10(8):e004761. doi: 10.1136/jitc-2022-004761
129. De Santis M, Mottet N, Cornford P, Gillessen S. Precision oncology for metastatic prostate cancer: Translation into practice. Eur Urol. (2020) 78(6):771–4. doi: 10.1016/j.eururo.2020.08.021
130. Smith DC, Smith MR, Sweeney C, Elfiky AA, Logothetis C, Corn PG, et al. Cabozantinib in patients with advanced prostate cancer: results of a phase II randomized discontinuation trial. J Clin Oncol (2013) 31(4):412–9. doi: 10.1200/JCO.2012.45.0494
131. Smith M, De Bono J, Sternberg C, Le Moulec S, Oudard S, De Giorgi U, et al. Phase III study of cabozantinib in previously treated metastatic castration-resistant prostate cancer: COMET-1. J Clin Oncol (2016) 34(25):3005–13. doi: 10.1200/JCO.2015.65.5597
132. Patnaik A, Swanson KD, Csizmadia E, Solanki A, Landon-Brace N, Gehring MP, et al. Cabozantinib eradicates advanced murine prostate cancer by activating antitumor innate immunity. Cancer Discovery (2017) 7(7):750–65. doi: 10.1158/2159-8290.CD-16-0778
133. Castellano D, Apolo AB, Porta C, Capdevila J, Viteri S, Rodriguez-Antona C, et al. Cabozantinib combination therapy for the treatment of solid tumors: a systematic review. Ther Adv Med Oncol (2022) 14:17588359221108691. doi: 10.1177/17588359221108691
Keywords: prostate cancer, immunotherapy, vaccine therapy, targeted therapy, combination therapy
Citation: Liang H, Liu Y, Guo J, Dou M, Zhang X, Hu L and Chen J (2023) Progression in immunotherapy for advanced prostate cancer. Front. Oncol. 13:1126752. doi: 10.3389/fonc.2023.1126752
Received: 18 December 2022; Accepted: 13 February 2023;
Published: 28 February 2023.
Edited by:
Ran Xu, Second Xiangya Hospital, Central South University, ChinaReviewed by:
Di Gu, First Affiliated Hospital of Guangzhou Medical University, ChinaHaolong Li, University of California, San Francisco, United States
Copyright © 2023 Liang, Liu, Guo, Dou, Zhang, Hu and Chen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jun Chen, Y2hlbmp1bnhpbnhpYW5nQDE2My5jb20=
†These authors have contributed equally to this work and share first authorship