Hengyuan Li
Junjie Gao2,3
Minghao Zheng
Zhaoming Ye- 1Department of Orthopedics, Centre for Orthopedic Research, School of Medicine, Orthopedics Research Institute, Second Affiliated Hospital, Zhejiang University, Hangzhou, China
- 2Centre for Orthopaedic Research, School of Surgery, The University of Western Australia, Nedlands, WA, Australia
- 3Department of Orthopaedic Surgery, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China
Denosumab is a monoclonal antibody against RANK ligand for treatment of giant cell tumor of bone (GCTB). Clinical trials and case series have demonstrated that denosumab is relevant to beneficial tumor response and surgical down-staging in patients of GCTB. However, these trials or case series have limitations with a short follow-up. Recent increasing studies revealed that denosumab probably increased the local recurrence risk in patients treated with curettage. This may be caused by the thicken bone margin of tumor that trapped tumor cells from curettage. The direct bone formation by tumor cells in the margin after denosumab treatment also contributed to the local recurrence. in vitro studies showed denosumab resulted in a cytostatic instead of a true cytotoxic response on neoplastic stromal cells. More importantly, denosumab-treated GCTB exhibited morphologic overlap with malignancy, and a growing number of patients of malignant transformation of GCTB during denosumab treatment have been reported. The optimal duration, long term safety, maintenance dose, and optimum indications remain to be elucidated. With these concerns in mind, this review warns that the denosumab therapy of GCTB should be applied with caution.
Introduction
Giant cell tumor of bone (GCTB) is a primary intermediate bone tumor with a local aggressive behavior (1). It accounts for ~4–5% of all primary bone tumors, with peak incidence in the second to fourth decades of life (2, 3). GCTB has a rare tendency to metastasize, but there is a soaring risk of pulmonary metastasis in those advanced or recurrent patients (4).
The main treatment modality of GCTB is surgery, which includes en bloc resection and extensive curettage with adjuvants. Ideally, extensive curettage combined with high-speed burring and local adjuvants should be the first choice and achieves salvage of joint adjacent to the tumor, although it has a higher recurrence rate. En-bloc resection is recommended as for the tumors with far-ranging bone destruction and soft tissue extension. It minimizes the risk of local recurrence but correlates with a higher rate of surgical complications and functional impairment. The local recurrence rate of GCTB ranges from 27 to 65% for curettage alone, from 12 to 27% for curettage combined with adjuvants and from 0 to 12% for en-bloc resection (5–8).
The discovery of the crucial role of RANK/RANKL pathway in the pathogenesis of GCTB has given rise to the development of denosumab, a fully human monoclonal antibody against RANKL. As neoadjuvant therapy for advanced GCTB which is unresectable or where surgical resection probably results in severe morbidity, denosumab is the only medicine approved by US Food and Drug Administration (FDA) and the European Medicines Agency (9). Numerous clinical trials have shown denosumab correlates with beneficial tumor response (10–12). However, recent studies revealing a higher rate of recurrence and patients of sarcomatous transformation of GCTB after denosumab therapy are reported increasingly (13–15). We were the first who reported that RANK/RANKL pathway was essential in the pathogenesis of GCTB (16), herein, it is time to put vital information together to create a full-scale review for denosumab therapy.
Histopathology and Genetics of GCTB
The better understanding of histopathology and molecular biology has led to the progress of denosumab for GCTB (17). Grossly, GCTB is well-vascularized and friable in texture with a dark brown-to-reddish appearance. Cystic degeneration, hemosiderin deposition, and hemorrhage can be seen, especially common in larger tumors. Microscopically, GCTB are typically comprised of RANK-positive circular mononuclear cells, “reactive” rich RANK-positive multinucleated giant cells, “neoplastic” densely cellular spindled RANKL-positive stromal-like tumor cells, areas of sparse osteoid matrix and woven bone (16, 18). Clues gleaned from studies corroborate that stromal cells, representing an immature osteoblast phenotype which originates from mesenchymal stem cells, are the true neoplastic part of GCTB because of their capacity to grow in cell-culture setting from generation to generation and form GCTB in mice (19–21).
Concerning functional biology, although a variety of cytokines such as SDF-1, MCP-1, VEGF, or M-CSF are involved, RANKL seems to be a core factor in the pathogenesis of GCTB (22). Overexpression of RANKL by stromal cells not only promotes recruiting monocyte precursors but also assists to form multinucleated osteoclast-like giant cells (23). Compared with RANK, denosumab has higher specificity and affinity to RANKL. As a result, denosumab could interrupt the RANK-RANKL binding which is necessary for osteoclast formation, leading to the elimination of osteoclast-like giant cells.
Karyotype analyses of tumor specimens displayed that chromosomal aberrations, including deletion, insertion, translocation, and other numerical or structural chromosomal rearrangement, are the common feature of GCTB (24, 25). Telomeric associations, where two diverse chromosome arms fuse together at ends, is the most prevailing cytogenetic finding. These associations are present in at least 70% of patients (24) and also found in isolated stromal cells (26). Telomeric associations are relevant to aberrations of clonal chromosome and reduction of telomere length, suggesting that telomeric instability is probably considered a vital core factor in the pathogenesis of GCTB (27, 28). However, no definite correlation between these cytogenetic abnormalities and established clinical grading systems or unfavorable clinical prognosis has been established (24, 25).
Recently, a distinct driver mutation H3F3A encoding the histone variant H3.3 has been identified in GCTB, with G34W accounting for the vast majority and G34L for a small minority (29, 30). This mutation is found in virtually all GCTBs, ranging from 92.0 to 97.8% (30, 31). It is confined to stromal cells and not detected in osteoclasts or precursors. IHC expression of G34W is more specific, sensitive and valuable for differential diagnosis from other histologically ambiguous giant cell-rich lesions including chondroblastoma, malignant giant cell-rich osteosarcoma and aneurysmal bone cyst. Even in metastatic, recurrent, secondary malignant and post-denosumab GCTBs, H3F3A G34W mutation and its IHC expression are maintained (32). Knockdown of this mutation counteracts the neoplastic phenotype, implying that H3F3A-G34W is sufficient to drive tumorigenesis of GCTB (33). Although mechanisms by which this mutation might drive tumorigenesis are still not fully understood, H3F3A-G34W presents a promising target for novel GCTB therapy.
Outcomes of Clinical Trials and Case Series on GCTB After Denosumab Treatment
The discovery of giant cells in GCTB expressing RANKL (16, 18) has led to the clinical application of denosumab in treatment of surgical undecidable tumor. Consequently, a first open-label phase II proof-of-concept study was conducted in Thomas et al. (10), who reported that 30 of 35 (86%) of patients had a tumor response to denosumab treatment, defined as at least 90% elimination of giant cells on histological evaluation or lack of radiological progression of the target lesion. However, this study contains a small sample size of selected population and only a small part of patients received intralesional curettage after denosumab. A second phase II study evaluating denosumab in 282 patients confirmed the efficacy and safety of denosumab in GCTB (11). One hundred and sixty three of 169 (96%) patients with surgically unsalvageable disease (cohort 1) had no disease progression after denosumab treatment. Of 100 patients with planned surgery (cohort 2), 16 of 26 patients underwent less morbid surgery than originally schemed, and 74% of patients had no surgery. The authors concluded that denosumab was effective and can prevent or reduce the morbidity of the planned surgery. However, the follow-up of roughly 1 year (median, 13 months for cohort 1, 9.2 months for cohort 2) is too short to reliably prove efficacy and safety in complicated cases of GCTB. It is noteworthy that sponsor Amgen was strongly involved in study design, assessment, and interpretation of data with potential bias. Another clinical trial of open-label phase II accessed the reduction in surgical invasiveness after denosumab therapy (34). Forty-eight percentage of 222 patients had no surgery or a less morbid procedure. Of the 116 patients who underwent surgery, 17 patients (15%) developed local recurrence. The median duration of follow-up for patients received surgery was 13 months. The median duration to recurrence was 13.6 months, postoperatively. Longitudinal institutional cases and collaborative group studies showed that local recurrence was inclined to occur principally within the first 12–18 months after surgery (35–37). Notably, the median follow-up of this study was insufficient, even shorter than that in local recurrence cases. Recently, Chawla et al. (12) presented the long-term follow-up results of their phase 2 trial of denosumab. They expanded the trial from 282 patients in the interim analysis (11) to 532 patients, and thereby completed the largest clinical trial to date on GCTB using denosumab. The authors showed that only 11% of patients with unresectable disease had progression after 65.8 medium months follow-up and 92% of the resectable patients had no surgery for GCTB during the first 6 months. However, 31 (34%) of 90 patients with resectable GCTB had tumor recurrence after curettage. Notably, 20 (4%) patients with a possible diagnosis of malignancy were identified. Although three-quarters of these patients were excluded from sarcomatous transformation since authors believed they had been misdiagnosed at baseline, the dubious association between denosumab and malignant transformation was still the event of great interest. To sum up, although these clinical trials presented promising results of denosumab in GCTB, it should be interpreted with caution by reason of short follow-ups, high risk of recurrence, potential malignant transformation and possible interference of funder.
Denosumab May Increase the Risk of Local Recurrence in Patients of GCTB Treated With Curettage
GCTB usually leads to expanded and thinned cortical bone at diagnosis, which could be prone to perforation with minimal pressure at surgical resection or curettage. After an average of 3–4 months of denosumab, a reduction in tumor size and the new ossified tumor matrix can be seen (38). It seems that neoadjuvant denosumab could promote en bloc resection and intralesional curettage via developing a calcified rim around the whole tumor and its soft tissue component. However, the local recurrence of curettage with neoadjuvant denosumab fails to be improved, even getting worse. In a prospective non-randomized study of patients who received denosumab for 6–11 months before intralesional curettage surgery, Traub et al. (39) reported a local recurrence rate of 17% (3/18) with the median follow-up of 30 months (range, 20–45 months). The local recurrence rate was comparable with those in other studies without denosumab treatment, indicating that denosumab may not improve local control of GCTB after curettage.
Errani et al. (13) reported a higher local recurrence rate in the cohort at a median follow-up of 42.1 months (range, 37.4–50.8 months). The local recurrence rate was as high as 60% (15/25) of patients with denosumab and curettage compared with 16% (36/222) of patients with isolated curettage. Denosumab was the only independent element correlated with a poor prognosis in view of recurrence-free survival. Although causation may not be evaluated by reason of substantial differences in the cohorts, such a high local recurrence rate dampens the enthusiasm and pushes us to reconsider the role of denosumab in curettage.
Other studies confirmed these results (Table 1). Agarwal et al. (15) conducted a case-matched comparison study to rule out some confusion involving denosumab. They reported that 44% (11/25) of patients in the denosumab and curettage group had local recurrences in comparison with 21% (7/34) in the control group without denosumab, although it was not statistically significant. They recommended to reduce the doses of denosumab before curettage to just adequate for bone formation and believed that it was crucial to curette and burr up to margins on initial images with the help of intraoperative C-am.
Table 1. Summary of published studies reporting higher local recurrence rate of GCTB after neoadjuvant denosumab following curettage.
We have speculated that denosumab treatment results in less removal of osseous tumor matrix and thus thickened tumor margin wall. As a result, the outline the true scope of tumors is no longer exist. In addition, tumor cells may be entrapped within the thickened new bone. In support of this, Muller et al. (44) revealed that viable tumor cells persisted in the new-formed bone induced by denosumab by means of histologic analysis. They suggested that the surgical technique of curettage had to be more aggressive to reduce higher local recurrence rate. Cryotherapy was recommended because the penetration depth in the adjacent bone was likely the best. However, in a retrospective study of patients with GCTB who received curettage and cryotherapy, Scoccianti et al. (40) showed a recurrence rate of 41.7% in 12 patients received denosumab in comparison to 11.1% in 9 patients in the surgery-only group, although it was not statistically significant. Puri et al. (41) revealed a recurrence rate of 29% in 41 patients who received preoperative denosumab with a mean follow-up of 34 months. Local recurrence occurred in 44% (11/25) of patients who had curettage, much higher than the resection group (1/16, 6%). Medellin et al. (42) conducted a study of 107 patients with pathological fracture due to GCTB, aiming to explore the prognostic factors for local recurrence. All patients who received denosumab combined with curettage, albeit only 4 cases, developed local recurrence. The authors found that denosumab was the only independent factor relevant to local recurrence by multivariate analysis, although the other two factors, the initial type of treatment and the location of the tumor, played roles on univariate analysis. Chinder et al. (43) conducted a study of 123 patients to evaluate the local recurrence of neoadjuvant denosumab following extensive curettage. This study was well-matched for the site of tumor and the type of surgery. The local recurrence rate in denosumab group is 42.8% (18/42), significantly higher than that of 18.5% (15/81) in curettage alone group. On multivariate analysis, neoadjuvant denosumab was the only independent risk factor for local recurrence following curettage. Recently, Tsukamoto et al. (45) performed a systematic analysis of seven studies with 619 patients and showed that the proportion of patients with local recurrence ranged from 20 to 100% in the curettage with preoperative denosumab compared with 0–50% in the curettage-alone group. The authors believed denosumab may be associated with an increase in local recurrence although the evidence was weak due to lack of randomized studies and indication bias. In another meta-analysis covering 10 studies with 1,082 cases, Chen et al. (46) found that denosumab therapy was correlated with higher local recurrence rate and inferior 5-year recurrence-free survival.
Several in vitro studies focused on the osteoclastogenic properties and viability of neoplastic stromal cells following denosumab therapy. Mak et al. (47) revealed that proliferation of stromal cells was only diminished by denosumab; once the micro-environment was free of the RANKL antibody, stromal cells remained proliferative, albeit to a lesser degree (~50% slower). Shibuya et al. (48) isolated three types of cells from GCTB patients and displayed that denosumab inhibited osteoclast differentiation and bone resorption but had no inhibitory effects on survival of osteoclasts or proliferation of stromal cells. Another study in comparison with zoledronic acid also showed that denosumab lacked anti-tumor effect against neoplastic stromal cells and raised a concern that local recurrence may occur in case of drug withdrawal (49).
The high rate of local recurrence after denosumab treatment may be interpreted as follows. Firstly, denosumab only targets multinucleated osteoclastic cells, rather than stromal cells. The neoplastic cells of GCTB still exist and has partial functions after denosumab therapy. Secondly, the typical soft tissue tumor of GCTB is altered into a gritty fibro-osseous matrix by denosumab treatment. That results in the tumor less defined from the ambient normal bone macroscopically and microscopically, making the decision of the extent of surgical curettage more intractable. In addition, denosumab also gives rise to thickening of the subchondral and cortical bone. As the circumferential bony layer thickens, it is probably that tumor cells get trapped within the new bone. Curettage is restricted by a thick bony shell to burr against. That most likely leads to tumor being inadvertently left behand after curettage and contributes to the local recurrence.
Some studies suggested that one of methods to promote identification of the boundary of tumor area and tissue response induced by denosumab is the usage of intra-operative fluoroscopy (15, 39). Using a C-arm intraoperatively, Agarwal et al. (15) reported a decreased recurrence rate from 57% (8/4) to 26% (6/23). They highlighted the importance of curettage to margins on pretreatment imaging. A shorter duration and lower doses of neoadjuvant therapy were also presented to reduce the risk of recurrence (9, 15, 38, 50). Maximum 3–4 months was deemed as the optimum time frame before intralesional surgery, considering that 6 months made the possibility of recurrence rate higher by getting the bony shell thicker and trapping more tumor cells. Hindiskere et al. (51) found that there were no significant differences between short-course (there or fewer doses) and long-course (more than three doses) groups of preoperative denosumab in terms of clinical scores, histological and radiological response or local recurrence survivorship. Short-course could reduce costs and complications linked with long-course therapy. However, Tsukamoto et al. (45) found that the preoperative denosumab duration did not seem to be associated with local recurrence after curettage by a systematic analysis of previous studies. Currently, the Japan Clinical Oncology Group is undertaking a randomized Phase III trial with 106 patients to ascertain the effect of preoperative denosumab on recurrence following curettage (52). More larger, multicenter and ideally prospective trials are warranted to reach concrete conclusions.
Denosumab May Arouse the Malignant Transformation of GCTB
The potential for malignant transformation of GCTB is a rare but crucial consideration. Malignant GCTB was first described 80 years ago (53). Histologically, it could be a fibrosarcoma, osteosarcoma or undifferentiated high-grade pleomorphic sarcoma (54). Malignant GCTB is considered as either primary or secondary and comprises about 4% of all GCTB (55). Primary cases are adjacent to benign GCTB and secondary ones develop from previously treated GCTB. Most malignant GCTB is secondary with a poor prognosis. Five-year disease-free survival of secondary GCTB was 32% (56). Multiple local recurrences and previous radiation therapy have been proposed as predisposing factors for malignant transformation (54, 55). Recently, cases of malignant transformation of GCTB during denosumab treatment have been reported growingly (Table 2). Thomas et al. (10) reported the first cases in the initial phase II study. New sarcomas occurred in two patients; one developed a high-grade sarcoma in the upper extremity during denosumab therapy and the other had a malignant GCTB with lung metastases after ceasing denosumab. In the second phase II study (11), new primary sarcomas occurred in two patients: one was deemed as a malignant transformation while the other was suspected to be present at baseline retrospectively. In the study of 222 patients of GCTB who received denosumab therapy, Rutkowski et al. (34) reported that four patients developed malignant transformation. Two of them were considered as radiation-associated sarcomatous transformation and the diagnosis of the other two was missed by sampling error at initial core biopsy. Broehm et al. (57) showed that two patents receiving denosumab developed malignant transformation of GCTB to osteosarcoma. Before sarcomatous transformation occurred, both patients responded to denosumab well. Aponte-Tinao et al. (14) reported a high-grade sarcoma arising in a woman aged 20 with a recurrent GCTB while receiving denosumab. Park et al. (58) presented a patient with a large GCTB of pelvis who received denosumab therapy. Seven months after surgical excision, the patient developed an osteosarcoma in the same site, along with pulmonary metastasis. Tsukamoto et al. (59) demonstrated a 25-year-old woman with recurrent GCTB in her left ischium developed a high grade osteosarcoma. She received denosumab therapy for 6 months. Agarwal et al. (15) reported that a patient with a proximal humerus GCTB developed osteosarcoma after 8 months of curettage, and then developed pulmonary metastases and died of disease. Chen et al. (60) reported that a male patient aged 43 with sacral GCTB developed secondary malignancy by postoperative pathological examination. This patient received 4 doses of denosumab before surgery and responded well. However, the tumor progressed rapidly and led to his death after 6 months. In the largest clinical trial to date on GCTB using denosumab, Chawla et al. (12) reported that 20 (4%) of 532 patients developed new malignancies. Fifteen cases were excluded from malignant transformation since authors believed they had been misdiagnosed at baseline, the other five were determined to be secondary malignant GCTB or sarcomatous transformation.
Table 2. Summary of published studies reporting malignant transformation of GCTB after denosumab therapy.
In these above-mentioned cases, all patients responded to denosumab until malignant transformation occurred. To the best of our knowledge, up to now, about 18 cases of malignant transformation of GCTB during denosumab treatment have been reported. Obviously, the cases are rare, and thus it cannot be concluded that there is a definite direct cause-and-effect correlation between denosumab and malignant transformation. Since radiotherapy was thought to be closely correlated with malignant transformation of GCTB (55), we could make a comparison of time interval from the start of therapy to diagnosis of malignant transformation between denosumab and radiotherapy. In the above-mentioned cases, the interval from start of denosumab to diagnosis of the malignancy was 0.2–2.8 years with the mean of 1.1 years. Bertoni et al. (61) reported that six patients of GCTB who received radiotherapy developed malignant transformation. The interval from start of radiotherapy to diagnosis of the malignancy was 1.7–15 years with the mean of 8 years. Apparently, the interval of denosumab is much shorter than that of radiotherapy.
The potential mechanisms of sarcomatous transformations of GCTB following denosumab therapy are probably associated with its actions against RANKL (59). Although the exact molecular basis is poorly defined, three possible hypotheses are proposed. Firstly, it has been questioned if denosumab affects immunity and inflammation, since RANKL plays critical roles in lymphocyte development and lymph-node organogenesis (62–64). The inhibition of RANKL could increase the risk of new malignancies as a result of immunosuppression. Secondly, in osteosarcoma cells, RANKL expression increases the level of nuclear factor IB (NKIB) (65), a transcription factor which exhibits tumor suppressive functions in many malignancies via down-regulating susceptibility to nuclear oncogenes (66). Thus, restraint of RANKL could lead to osteosarcoma carcinogenesis by raising susceptibility to nuclear oncogenes. Thirdly, RANKL upregulates the level of Sema3A gene in osteosarcoma (65), and deletion of this gene could lead to aberrant cartilage and bone growth (67, 68). As a result, it is possible that restraint of RANKL by denosumab induces aberrant osteoblasts differentiation and osteosarcoma tumorigenesis via Sema3A.
Morphological, Immunohitochemical and Molecular Changes of GCTB After Denosumab Therapy
The histologic changes of GCTB after denosumab treatment are variable and consist of depletion of giant cells, a reduction of neoplastic stromal cells, and incremental fibro-osseous tissue and/or new woven bone. We even found the ectopic osteoid formation in lung tissue of denosumab-treated patient following GCTB metastasis (Figure 1). These changes are so dramatic that the lesions treated by denosumab do not have any resemblance to the original ones and it is probably confused with malignant tumors. Wojcik et al. (69) examined 9 cases of denosumab-treated GCTB and demonstrated that tumor samples zexhibited morphologic overlap with malignancy. Early lesions were highly cellular and the combination of cellularity, atypia, and haphazard bone deposition were reminiscent of high-grade osteosarcoma. Lesions of prolonged therapy displayed decreased cellularity and abundant new bone, resembling low-grade central osteosarcoma. However, Roitman et al. (70) failed to find a clear association between treatment length of denosumab and extent of histologic changes. They reviewed histologic slides of 9 patients receiving denosumab and revealed that cellular atypia or patterns of ossification was less frequent but more relevant. These histologic feathers resemble an undifferentiated pleomorphic sarcoma, a conventional osteosarcoma or a low-grade central osteosarcoma. The Pseudosarcomatous changes were also described by Santosh et al. (71). A pseudosarcomatous spindle cell proliferation with osteoid matrix might have been confused with osteosarcoma after 9 cycles of denosumab therapy. In another case report of GCTB in the distal ulna, Sanchez-Pareja et al. (72) presented that densely cellular foci with atypical cells and osteoid deposition mimicked high-grade osteosarcoma after 6 weeks of denosumab treatment. They emphasized the difficulty in histologic evaluation of GCTB early in the course of denosumab treatment.
Figure 1. Ectopic osteoid formation in lung tissue of denosumab-treated patient following GCTB metastasis. (A) α zone, GCTB, β zone, fibroblastic osteoid-forming, γ zone, pulmonary tissue, arrow, osteoid. (B) β zone, fibroblastic osteoid-forming, arrow, osteoclastic cells. Hematoxylin and eosin statin, magnifications ×100 (A), ×400 (B).
What accounts for the dramatic histological changes caused by denosumab? It appears to reflect a shift in the balance from RANK-mediated osteoclastic bone resorption to bone formation induced by stromal cells after denosumab therapy. Under physiological conditions, it is osteoclasts that induce osteoblastic bone formation by various growth factors including TGF-β and IGF-1 in the context of bone remodeling (73). In GCTB, however, the osteoclasts probably suppress the osteogenic differentiation of stromal cells via various mediating factors (32, 74). After denosumab therapy, both osteoclast maturation from precursors and function are blocked due to the inhibition of RANK/RANKL axis. Therefore, new balance may be in favor of bone formation, allowing surviving stromal cells to undrape their osteogenic nature in the microenvironment free of osteoclasts. However, this shift does not reflect the terminal differentiation of stromal cells which has a preosteoblast phenotype since the morphology reverts to classic GCTB after withdrawal of denosumab treatment (23).
Mukaihara et al. (75) performed comparative proteomic analyses to explore molecular mechanisms underlying the therapeutic effect of denosumab. They identified five most dysregulated proteins, MMP9, LUM, KCRB, CAH2, PPA5. The first two were associated with the local aggressive behavior of GCTB (76, 77). The last three had crucial roles in osteoclast-mediated bone resorption (76, 78, 79). Kato et al. (80) revealed that all lesions treated by denosumab still contained plenty of G34W+ cells and harbored H3F3A mutations, indicating that neoplastic cells survived the denosumab therapy. Girolami et al. (81) displayed a significant reduction of microvessel density in GCTB after denosumab treatment although the underlying mechanism responsible for the antiangiogenic effect needed to be further expounded.
How Long Should Denosumab Therapy be Continued?
Despite numerous trials involving denosumab for the treatment of GCTB, much about the optimal therapy duration remains unknown. There is a major concern that cessation of denosumab correlates with a higher rate of subsequent local recurrence (47). Palmerini et al. (82) revealed that after a median of 8 months with the range from 7 to 15 months of discontinuing denosumab, 40% of patients of GCTB had tumor progression. Matcuk et al. (83) presented a case report of rapid recurrence of GCTB in a woman aged 24 after the discontinuation of long-term denosumab therapy. The patient had good and sustained tumor control for over 2 years during denosumab therapy. However, only within 2 months of cessation, the tumor showed rapid recurrence and progression with growth. Worse still, it was resistant to reinitiating denosumab therapy, ultimately necessitating below-the-elbow amputation. The authors, therefore, recommended life-long denosumab therapy. In the largest clinical trial on GCTB using denosumab, Chawla et al. (12) reported that 26% (34/132) of surgically unsalvageable patients had disease recurrence or progression after cessation of denosumab. The authors recommended a reduced dose or less frequent administration of denosumab for maintenance in patients with unresectable GCTB. Therefore, it is critical and urgent to evaluate the risk of relapse following denosumab cessation in the prospective clinical trials. If the tumor recurrence is inevitable after drug withdraw, patients have to receive life-long treatment. Lingering unknowns on long term safety, the optimal maintenance dose and frequency schedule and therapeutic strategy for female patients of baby-bearing age remain to be explored.
Conclusions
In the initial trials, Denosumab was deemed as an exciting, new targeted therapy option for patients with GCTB. The usage of neoadjuvant denosumab aims to facilitate surgery, making intralesional curettage or resection technically easier and feasible, thereby hoping for local tumor control. However, more and more studies displayed the negative effects of denosumab therapy on GCTB. (1) Denosumab selectively targeted osteoclastic cells but had limited inhibitory effect on neoplastic stromal cells, which persisted and remained proliferative on cessation of drug. (2) Denosumab may increase the risk of local recurrence in patients of GCTB treated with curettage. The thickened new bone induced by denosumab, in which tumor cells got trapped, made it difficult for surgeon to delineate the true extent of the tumor and curettage adequately. As a result, if curettage is feasible, we do not recommend using preoperative denosumab, unless the benefit outweighs the possibility of local recurrence. (3) Denosumab may cause the malignant transformation of GCTB. GCTB is a benign tumor in a young population and rarely life threatening even if lung metastasis occurs. However, despite low incidence rate and unknown mechanisms, sarcomatous transformation induced by denosumab has a poor outcome, which is a fatal blow to young patients. Based on these negative effects and unanswered questions regarding optimal use of denosumab, we recommended strongly application of this drug with caution for the treatment of GCTB, only when the burden of down-staging to perform a lesser morbid procedure outweighs the potential chance of local recurrence. Collaborative clinical trials and rigorous data collection are mandated to identify the optimum indications for using denosumab in GCTB and to ascertain the role that denosumab plays in malignant transformation and high recurrence risk.
Author Contributions
HL wrote most of the manuscript. JG and YG made the figures and tables. MZ conceived and revised the manuscript. NL and ZY thoroughly revised and amended the manuscript. 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.
Acknowledgments
Lianzhi Chen helped in preparing the figure of the manuscript.
References
1. Fletcher CDM, Bridge JA, Hogendoorn PCW, Mertens F. WHO Classification of Tumours of Soft Tissue and Bone. 4ed. Lyon: International Agency for Research on Cancer (IARC) (2013). p. 321–4.
2. Campanacci M, Baldini N, Boriani S, Sudanese A. Giant-cell tumor of bone. J Bone Joint Surg Am. (1987) 69:106–14. doi: 10.2106/00004623-198769010-00018
3. Liede A, Bach BA, Stryker S, Hernandez RK, Sobocki P, Bennett B, et al. Regional variation and challenges in estimating the incidence of giant cell tumor of bone. J Bone Joint Surg Am. (2014) 96:1999–2007. doi: 10.2106/JBJS.N.00367
4. Chan CM, Adler Z, Reith JD, Gibbs CP. Risk factors for pulmonary metastases from giant cell tumor of bone. J Bone Joint Surg Am. (2015) 97:420–8. doi: 10.2106/JBJS.N.00678
5. Arbeitsgemeinschaft K, Becker WT, Dohle J, Bernd L, Braun A, Cserhati M, et al. Local recurrence of giant cell tumor of bone after intralesional treatment with and without adjuvant therapy. J Bone Joint Surg Am. (2008) 90:1060–7. doi: 10.2106/JBJS.D.02771
6. Algawahmed H, Turcotte R, Farrokhyar F, Ghert M. High-speed burring with and without the use of surgical adjuvants in the intralesional management of giant cell tumor of bone: a systematic review and meta-analysis. Sarcoma. (2010) 2010:586090. doi: 10.1155/2010/586090
7. Balke M, Schremper L, Gebert C, Ahrens H, Streitbuerger A, Koehler G, et al. Giant cell tumor of bone: treatment and outcome of 214 cases. J Cancer Res Clin Oncol. (2008) 134:969–78. doi: 10.1007/s00432-008-0370-x
8. Errani C, Ruggieri P, Asenzio MA, Toscano A, Colangeli S, Rimondi E, et al. Giant cell tumor of the extremity: a review of 349 cases from a single institution. Cancer Treat Rev. (2010) 36:1–7. doi: 10.1016/j.ctrv.2009.09.002
9. Gaston CL, Grimer RJ, Parry M, Stacchiotti S, Dei Tos AP, Gelderblom H, et al. Current status and unanswered questions on the use of Denosumab in giant cell tumor of bone. Clin Sarcoma Res. (2016) 6:15. doi: 10.1186/s13569-016-0056-0
10. Thomas D, Henshaw R, Skubitz K, Chawla S, Staddon A, Blay JY, et al. Denosumab in patients with giant-cell tumour of bone: an open-label, phase 2 study. Lancet Oncol. (2010) 11:275–80. doi: 10.1016/S1470-2045(10)70010-3
11. Chawla S, Henshaw R, Seeger L, Choy E, Blay JY, Ferrari S, et al. Safety and efficacy of denosumab for adults and skeletally mature adolescents with giant cell tumour of bone: interim analysis of an open-label, parallel-group, phase 2 study. Lancet Oncol. (2013) 14:901–8. doi: 10.1016/S1470-2045(13)70277-8
12. Chawla S, Blay JY, Rutkowski P, Le Cesne A, Reichardt P, Gelderblom H, et al. Denosumab in patients with giant-cell tumour of bone: a multicentre, open-label, phase 2 study. Lancet Oncol. (2019) 20:1719–29. doi: 10.1016/S1470-2045(19)30663-1
13. Errani C, Tsukamoto S, Leone G, Righi A, Akahane M, Tanaka Y, et al. Denosumab may increase the risk of local recurrence in patients with giant-cell tumor of bone treated with curettage. J Bone Joint Surg Am. (2018) 100:496–504. doi: 10.2106/JBJS.17.00057
14. Aponte-Tinao LA, Piuzzi NS, Roitman P, Farfalli GL. A high-grade sarcoma arising in a patient with recurrent benign giant cell tumor of the proximal tibia while receiving treatment with denosumab. Clin Orthop Relat Res. (2015) 473:3050–5. doi: 10.1007/s11999-015-4249-2
15. Agarwal MG, Gundavda MK, Gupta R, Reddy R. Does denosumab change the giant cell tumor treatment strategy? Lessons learned from early experience. Clin Orthop Relat Res. (2018) 476:1773–82. doi: 10.1007/s11999.0000000000000243
16. Huang L, Xu J, Wood DJ, Zheng MH. Gene expression of osteoprotegerin ligand, osteoprotegerin, and receptor activator of NF-kappaB in giant cell tumor of bone: possible involvement in tumor cell-induced osteoclast-like cell formation. Am J Pathol. (2000) 156:761–7. doi: 10.1016/S0002-9440(10)64942-5
17. Lacey DL, Boyle WJ, Simonet WS, Kostenuik PJ, Dougall WC, Sullivan JK, et al. Bench to bedside: elucidation of the OPG-RANK-RANKL pathway and the development of denosumab. Nat Rev Drug Discov. (2012) 11:401–19. doi: 10.1038/nrd3705
18. Branstetter DG, Nelson SD, Manivel JC, Blay JY, Chawla S, Thomas DM, et al. Denosumab induces tumor reduction and bone formation in patients with giant-cell tumor of bone. Clin Cancer Res. (2012) 18:4415–24. doi: 10.1158/1078-0432.CCR-12-0578
19. Byers VS, Levin AS, Johnston JO, Hackett AJ. Quantitative immunofluorescence studies of the tumor antigen-bearing cell in giant cell tumor of bone and osteogenic sarcoma. Cancer Res. (1975)35:2520–31.
20. Atkins GJ, Haynes DR, Graves SE, Evdokiou A, Hay S, Bouralexis S, et al. Expression of osteoclast differentiation signals by stromal elements of giant cell tumors. J Bone Miner Res. (2000) 15:640–9. doi: 10.1359/jbmr.2000.15.4.640
21. Wulling M, Delling G, Kaiser E. The origin of the neoplastic stromal cell in giant cell tumor of bone. Hum Pathol. (2003) 34:983–93. doi: 10.1053/S0046-8177(03)00413-1
22. Noh BJ, Park YK. Giant cell tumor of bone: updated molecular pathogenesis and tumor biology. Hum Pathol. (2018) 81:1–8. doi: 10.1016/j.humpath.2018.06.017
23. Cowan RW, Singh G. Giant cell tumor of bone: a basic science perspective. Bone. (2013) 52:238–46. doi: 10.1016/j.bone.2012.10.002
24. Gorunova L, Vult von Steyern F, Storlazzi CT, Bjerkehagen B, Folleras G, Heim S, et al. Cytogenetic analysis of 101 giant cell tumors of bone: nonrandom patterns of telomeric associations and other structural aberrations. Genes Chromosomes Cancer. (2009) 48:583–602. doi: 10.1002/gcc.20667
25. Bridge JA, Neff JR, Bhatia PS, Sanger WG, Murphey MD. Cytogenetic findings and biologic behavior of giant cell tumors of bone. Cancer Am Cancer Soc. (1990) 65:2697–703. doi: 10.1002/1097-0142(19900615)65:12<2697::AID-CNCR2820651217>3.0.CO;2-3
26. Zheng MH, Siu P, Papadimitriou JM, Wood DJ, Murch AR. Telomeric fusion is a major cytogenetic aberration of giant cell tumors of bone. Pathology. (1999) 31:373–8. doi: 10.1080/003130299104756
27. Gebre-Medhin S, Broberg K, Jonson T, Gorunova L, von Steyern FV, Brosjo O, et al. Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone. Cytogenet Genome Res. (2009) 124:121–7. doi: 10.1159/000207516
28. Forsyth RG, De Boeck G, Bekaert S, De Meyer T, Taminiau AH, Uyttendaele D, et al. Telomere biology in giant cell tumour of bone. J Pathol. (2008) 214:555–63. doi: 10.1002/path.2301
29. Behjati S, Tarpey PS, Presneau N, Scheipl S, Pillay N, Van Loo P, et al. Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone. Nat Genet. (2013) 45:1479–82. doi: 10.1038/ng.2814
30. Amary F, Berisha F, Ye H, Gupta M, Gutteridge A, Baumhoer D, et al. H3F3A (Histone 3.3) G34W immunohistochemistry: a reliable marker defining benign and malignant giant cell tumor of bone. Am J Surg Pathol. (2017) 41:1059–68. doi: 10.1097/PAS.0000000000000859
31. Nohr E, Lee LH, Cates JM, Perizzolo M, Itani D. Diagnostic value of histone 3 mutations in osteoclast-rich bone tumors. Hum Pathol. (2017) 68:119–27. doi: 10.1016/j.humpath.2017.08.030
32. Yamamoto H, Iwasaki T, Yamada Y, Matsumoto Y, Otsuka H, Yoshimoto M, et al. Diagnostic utility of histone H3.3 G34W, G34R, and G34V mutant-specific antibodies for giant cell tumors of bone. Hum Pathol. (2018) 73:41–50. doi: 10.1016/j.humpath.2017.11.020
33. Fellenberg J, Sahr H, Mancarella D, Plass C, Lindroth AM, Westhauser F, et al. Knock-down of oncohistone H3F3A-G34W counteracts the neoplastic phenotype of giant cell tumor of bone derived stromal cells. Cancer Lett. (2019) 448:61–9. doi: 10.1016/j.canlet.2019.02.001
34. Rutkowski P, Ferrari S, Grimer RJ, Stalley PD, Dijkstra SP, Pienkowski A, et al. Surgical downstaging in an open-label phase II trial of denosumab in patients with giant cell tumor of bone. Ann Surg Oncol. (2015) 22:2860–8. doi: 10.1245/s10434-015-4634-9
35. Gaston CL, Bhumbra R, Watanuki M, Abudu AT, Carter SR, Jeys LM, et al. Does the addition of cement improve the rate of local recurrence after curettage of giant cell tumours in bone? J Bone Joint Surg Br. (2011) 93:1665–9. doi: 10.1302/0301-620X.93B12.27663
36. Prosser GH, Baloch KG, Tillman RM, Carter SR, Grimer RJ. Does curettage without adjuvant therapy provide low recurrence rates in giant-cell tumors of bone? Clin Orthop Relat Res. (2005) 435:211–8. doi: 10.1097/01.blo.0000160024.06739.ff
37. Kivioja AH, Blomqvist C, Hietaniemi K, Trovik C, Walloe A, Bauer HC, et al. Cement is recommended in intralesional surgery of giant cell tumors: a scandinavian sarcoma group study of 294 patients followed for a median time of 5 years. Acta Orthop. (2008) 79:86–93. doi: 10.1080/17453670710014815
38. van der Heijden L, Dijkstra PDS, Blay JY, Gelderblom H. Giant cell tumour of bone in the denosumab era. Eur J Cancer. (2017) 77:75–83. doi: 10.1016/j.ejca.2017.02.021
39. Traub F, Singh J, Dickson BC, Leung S, Mohankumar R, Blackstein ME, et al. Efficacy of denosumab in joint preservation for patients with giant cell tumour of the bone. Eur J Cancer. (2016) 59:1–12. doi: 10.1016/j.ejca.2016.01.006
40. Scoccianti G, Totti F, Scorianz M, Baldi G, Roselli G, Beltrami G, et al. Preoperative denosumab with curettage and cryotherapy in giant cell tumor of bone: is there an increased risk of local recurrence? Clin Orthop Relat Res. (2018) 476:1783–90. doi: 10.1007/s11999.0000000000000104
41. Puri A, Gulia A, Hegde P, Verma V, Rekhi B. Neoadjuvant denosumab: its role and results in operable cases of giant cell tumour of bone. Bone Joint J. (2019) 101:170–7. doi: 10.1302/0301-620X.101B2.BJJ-2018-0907.R2
42. Medellin MR, Fujiwara T, Tillman RM, Jeys LM, Gregory J, Stevenson JD, et al. Prognostic factors for local recurrence in extremity-located giant cell tumours of bone with pathological fracture. Bone Joint J. (2018) 100-B:1626–32. doi: 10.1302/0301-620X.100B12.BJJ-2018-0189.R2
43. Chinder PS, Hindiskere S, Doddarangappa S, Pal U. Evaluation of local recurrence in giant-cell tumor of bone treated by neoadjuvant denosumab. Clin Orthop Surg. (2019) 11:352–60. doi: 10.4055/cios.2019.11.3.352
44. Muller DA, Beltrami G, Scoccianti G, Campanacci DA, Franchi A, Capanna R. Risks and benefits of combining denosumab and surgery in giant cell tumor of bone-a case series. World J Surg Oncol. (2016) 14:281. doi: 10.1186/s12957-016-1034-y
45. Tsukamoto S, Tanaka Y, Mavrogenis AF, Kido A, Kawaguchi M, Errani C. Is treatment with denosumab associated with local recurrence in patients with giant cell tumor of bone treated with curettage? A systematic review. Clin Orthop Relat Res. (2020) 478:1076–85. doi: 10.1097/CORR.0000000000001074
46. Chen X, Li H, Zhu S, Wang Y, Qian W. Pre-operative denosumab is associated with higher risk of local recurrence in giant cell tumor of bone: a systematic review and meta-analysis. BMC Musculoskelet Disord. (2020) 21:256. doi: 10.1186/s12891-020-03294-2
47. Mak IW, Evaniew N, Popovic S, Tozer R, Ghert M. A translational study of the neoplastic cells of giant cell tumor of bone following neoadjuvant denosumab. J Bone Joint Surg Am. (2014) 96:e127. doi: 10.2106/JBJS.M.01332
48. Shibuya I, Takami M, Miyamoto A, Karakawa A, Dezawa A, Nakamura S, et al. In vitro study of the effects of denosumab on giant cell tumor of bone: comparison with zoledronic acid. Pathol Oncol Res. (2019) 25:409–19. doi: 10.1007/s12253-017-0362-8
49. Lau CP, Huang L, Wong KC, Kumta SM. Comparison of the anti-tumor effects of denosumab and zoledronic acid on the neoplastic stromal cells of giant cell tumor of bone. Connect Tissue Res. (2013) 54:439–49. doi: 10.3109/03008207.2013.848202
50. Rutkowski P, Gaston L, Borkowska A, Stacchiotti S, Gelderblom H, Baldi GG, et al. Denosumab treatment of inoperable or locally advanced giant cell tumor of bone - multicenter analysis outside clinical trial. Eur J Surg Oncol. (2018) 44:1384–90. doi: 10.1016/j.ejso.2018.03.020
51. Hindiskere S, Errani C, Doddarangappa S, Ramaswamy V, Rai M, Chinder PS. Is a Short-course of preoperative denosumab as effective as prolonged therapy for giant cell tumor of bone? Clin Orthop Relat Res. (2020). doi: 10.1097/CORR.0000000000001285. [Epub ahead of print].
52. Urakawa H, Mizusawa J, Tanaka K, Eba J, Hiraga H, Kawai A, et al. A randomized phase III trial of denosumab before curettage for giant cell tumor of bone: japan clinical oncology group study JCOG1610. Jpn J Clin Oncol. (2019) 49:379–82. doi: 10.1093/jjco/hyz004
53. Stewart FW, Coley BL, Farrow JH. Malignant giant cell tumor of bone. Am J Pathol. (1938) 14:515–36.
54. Gong L, Liu W, Sun X, Sajdik C, Tian X, Niu X, et al. Histological and clinical characteristics of malignant giant cell tumor of bone. Virchows Arch. (2012) 460:327–34. doi: 10.1007/s00428-012-1198-y
55. Palmerini E, Picci P, Reichardt P, Downey G. Malignancy in giant cell tumor of bone: a review of the literature. Technol Cancer Res Treat. (2019) 18:1533033819840000. doi: 10.1177/1533033819840000
56. Rock MG, Sim FH, Unni KK, Witrak GA, Frassica FJ, Schray MF, et al. Secondary malignant giant-cell tumor of bone. Clinicopathological assessment of nineteen patients. J Bone Joint Surg Am. (1986) 68:1073–9. -doi: 10.2106/00004623-198668070-00016
57. Broehm CJ, Garbrecht EL, Wood J, Bocklage T. Two cases of sarcoma arising in giant cell tumor of bone treated with denosumab. Case Rep Med. (2015) 2015:767198. doi: 10.1155/2015/767198
58. Park A, Cipriano CA, Hill K, Kyriakos M, McDonald DJ. Malignant transformation of a giant cell tumor of bone treated with denosumab: a case report. JBJS Case Connect. (2016) 6:e78. doi: 10.2106/JBJS.CC.16.00024
59. Tsukamoto S, Righi A, Vanel D, Honoki K, Donati DM, Errani C. Development of high-grade osteosarcoma in a patient with recurrent giant cell tumor of the ischium while receiving treatment with denosumab. Jpn J Clin Oncol. (2017) 47:1090–6. doi: 10.1093/jjco/hyx112
60. Chen Z, Yang Y, Guo W, Yang R, Tang X, Yan T, et al. Therapeutic benefits of neoadjuvant and post-operative denosumab on sacral giant cell tumor: a retrospective cohort study of 30 cases. J Buon. (2018) 23:453–9.
61. Bertoni F, Bacchini P, Staals EL. Malignancy in giant cell tumor of bone. Cancer-Am Cancer Soc. (2003) 97:2520–9. doi: 10.1002/cncr.11359
62. Ferrari-Lacraz S, Ferrari S. Do RANKL inhibitors (denosumab) affect inflammation and immunity? Osteoporos Int. (2011) 22:435–46. doi: 10.1007/s00198-010-1326-y
63. Kong YY, Yoshida H, Sarosi I, Tan HL, Timms E, Capparelli C, et al. OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis. Nature. (1999) 397:315–23. doi: 10.1038/16852
64. Smith MR, Egerdie B, Hernandez Toriz N, Feldman R, Tammela TL, Saad F, et al. Denosumab in men receiving androgen-deprivation therapy for prostate cancer. N Engl J Med. (2009) 361:745–55. doi: 10.1056/NEJMoa0809003
65. Mori K, Berreur M, Blanchard F, Chevalier C, Guisle-Marsollier I, Masson M, et al. Receptor activator of nuclear factor-kappaB ligand (RANKL) directly modulates the gene expression profile of RANK-positive Saos-2 human osteosarcoma cells. Oncol Rep. (2007) 18:1365–71. doi: 10.3892/or.18.6.1365
66. Becker-Santos DD, Lonergan KM, Gronostajski RM, Lam WL. Nuclear factor I/B: a master regulator of cell differentiation with paradoxical roles in cancer. EBioMedicine. (2017) 22:2–9. doi: 10.1016/j.ebiom.2017.05.027
67. Hayashi M, Nakashima T, Taniguchi M, Kodama T, Kumanogoh A, Takayanagi H. Osteoprotection by semaphorin 3A. Nature. (2012) 485:69–74. doi: 10.1038/nature11000
68. Behar O, Golden JA, Mashimo H, Schoen FJ, Fishman MC. Semaphorin III is needed for normal patterning and growth of nerves, bones and heart. Nature. (1996) 383:525–8. doi: 10.1038/383525a0
69. Wojcik J, Rosenberg AE, Bredella MA, Choy E, Hornicek FJ, Nielsen GP, et al. Denosumab-treated giant cell tumor of bone exhibits morphologic overlap with malignant giant cell tumor of bone. Am J Surg Pathol. (2016) 40:72–80. doi: 10.1097/PAS.0000000000000506
70. Roitman PD, Jauk F, Farfalli GL, Albergo JI, Aponte-Tinao LA. Denosumab-treated giant cell tumor of bone. Its histologic spectrum and potential diagnostic pitfalls. Hum Pathol. (2017) 63:89–97. doi: 10.1016/j.humpath.2017.02.008
71. Santosh N, Mayerson JL, Iwenofu OH. Pseudosarcomatous spindle cell proliferation with osteoid matrix mimicking osteosarcoma: a distinct histologic phenotype in giant cell tumor of bone following denosumab therapy. Appl Immunohistochem Mol Morphol. (2016) 24:e18–9. doi: 10.1097/PAI.0000000000000165
72. Sanchez-Pareja A, Larousserie F, Boudabbous S, Beaulieu JY, Mach N, Saiji E, et al. Giant cell tumor of bone with pseudosarcomatous changes leading to premature denosumab therapy interruption: a case report with review of the literature. Int J Surg Pathol. (2016) 24:366–72. doi: 10.1177/1066896916629546
73. Charles JF, Aliprantis AO. Osteoclasts: more than 'bone eaters'. Trends Mol Med. (2014) 20:449–59. doi: 10.1016/j.molmed.2014.06.001
74. Kubota K, Sakikawa C, Katsumata M, Nakamura T, Wakabayashi K. Platelet-derived growth factor BB secreted from osteoclasts acts as an osteoblastogenesis inhibitory factor. J Bone Miner Res. (2002) 17:257–65. doi: 10.1359/jbmr.2002.17.2.257
75. Mukaihara K, Suehara Y, Kohsaka S, Akaike K, Tanabe Y, Kubota D, et al. Protein expression profiling of giant cell tumors of bone treated with denosumab. PLoS ONE. (2016) 11:e0148401. doi: 10.1371/journal.pone.0148401
76. Lieveld M, Bodson E, De Boeck G, Nouman B, Cleton-Jansen AM, Korsching E, et al. Gene expression profiling of giant cell tumor of bone reveals downregulation of extracellular matrix components decorin and lumican associated with lung metastasis. Virchows Arch. (2014) 465:703–13. doi: 10.1007/s00428-014-1666-7
77. Rabinovich A, Mak IW, Cowan RW, Turcotte RE, Colterjohn N, Singh G, et al. Matrix metalloproteinase activity in the stromal cell of giant cell tumor of bone. Open Bone J. (2009) 1:46–52. doi: 10.2174/1876525400901010046
78. Chang EJ, Ha J, Oerlemans F, Lee YJ, Lee SW, Ryu J, et al. Brain-type creatine kinase has a crucial role in osteoclast-mediated bone resorption. Nat Med. (2008) 14:966–72. doi: 10.1038/nm.1860
79. Halleen JM, Tiitinen SL, Ylipahkala H, Fagerlund KM, Vaananen HK. Tartrate-resistant acid phosphatase 5b (TRACP 5b) as a marker of bone resorption. Clin Lab. (2006) 52:499–509.
80. Kato I, Furuya M, Matsuo K, Kawabata Y, Tanaka R, Ohashi K. Giant cell tumours of bone treated with denosumab: histological, immunohistochemical and H3F3A mutation analyses. Histopathology. (2018) 72:914–22. doi: 10.1111/his.13448
81. Girolami I, Mancini I, Simoni A, Baldi GG, Simi L, Campanacci D, et al. Denosumab treated giant cell tumour of bone: a morphological, immunohistochemical and molecular analysis of a series. J Clin Pathol. (2016) 69:240–7. doi: 10.1136/jclinpath-2015-203248
82. Palmerini E, Chawla NS, Ferrari S, Sudan M, Picci P, Marchesi E, et al. Denosumab in advanced/unresectable giant-cell tumour of bone (GCTB): for how long? Eur J Cancer. (2017) 76:118–24. doi: 10.1016/j.ejca.2017.01.028
Keywords: giant cell tumor of bone, denosumab, local recurrence risk, malignant transformation, H3F3A G34W
Citation: Li H, Gao J, Gao Y, Lin N, Zheng M and Ye Z (2020) Denosumab in Giant Cell Tumor of Bone: Current Status and Pitfalls. Front. Oncol. 10:580605. doi: 10.3389/fonc.2020.580605
Received: 07 July 2020; Accepted: 28 August 2020;
Published: 02 October 2020.
Edited by:
Giuseppe Di Lorenzo, Azienda Sanitaria Locale Salerno, ItalyReviewed by:
Yoshiyuki Suehara, Juntendo University, JapanCostantino Errani, Rizzoli Orthopedic Institute (IRCCS), Italy
Copyright © 2020 Li, Gao, Gao, Lin, Zheng and Ye. 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: Zhaoming Ye, yezhaoming@zju.edu.cn; Minghao Zheng, minghao.zheng@uwa.edu.au