Mingyu Wan1†
Yongfeng Ding1†
Chenyu Mao1Xiaolu Ma1Ning Li1Cheng Xiao1Jiong Qian1Haiping Jiang1Yulong Zheng1Luntao Wu1
Lisong Teng2
Nong Xu1*- 1Department of Medical Oncology, The First Affiliated Hospital of Zhejiang University, Hangzhou, China
- 2Department of Surgical Oncology, The First Affiliated Hospital of Zhejiang University, Hangzhou, China
Background: The emergence of immune checkpoint inhibitors has changed the landscape of first-line treatment of patients with advanced gastric cancer. Currently, the prognostic significance of inflammatory markers in first-line immunotherapy combined with chemotherapy for gastric cancer is currently unclear. This study aimed to identify inflammatory markers with potential to predict treatment outcome in advanced gastric cancer patients receiving immunotherapy combined with chemotherapy.
Methods: This retrospective study enrolled untreated advanced or metastatic gastric or gastro-esophageal junction cancer patients from 5 clinical trials (the clinical trial cohort) and the real world (the real-word cohort). Inflammatory markers included in the analysis included neutrophil-to-lymphocyte ratio (NLR), monocyte-to-lymphocyte ratio (MLR), platelet-to-lymphocyte ratio (PLR), systemic inflammation index (SII), and derived neutrophil-to-lymphocyte ratio (dNLR). Receiver operating characteristic (ROC) curves were constructed to identify optimal cut-off values. The prognostic potential of the markers was determined using Kaplan–Meier analysis, univariate and multivariate Cox-regression analyses in the clinical trial cohort and the findings were validated in the real-world cohort.
Results: In the clinical trial cohort (n=45), MLR, PLR and SII were associated with PFS but not OS (All P<0.05), while dNLR was not correlated with PFS or OS. Only NLR was associated with PFS and OS and identified as an independent prognostic predictor in the univariate and multivariate analyses. The prognostic value of NLR was validated in the real-world cohort (n=55).
Conclusions: NLR was a strong predictor of PFS and OS in patients with advanced gastric cancer receiving immune checkpoint inhibitors combined with chemotherapy. Further prospective studies are required to validate our results.
Introduction
Gastric cancer (GC) is the fourth leading cause of cancer-related deaths worldwide, with over one million new cases and 769,000 deaths reported in 2020 (1). Although, doublet fluoropyrimidine-based and platinum-based chemotherapy regimens are the preferred first-line treatments, immune checkpoint inhibitors in combination with chemotherapy are becoming the standard of care for patients with advanced gastric cancer (2–4). The 2-year follow-up data of the CheckMate 649 trial published at the 2021 ESMO Annual Meeting revealed that nivolumab combined with chemotherapy resulted in a longer OS (13.8 vs.11.6 months, HR: 0.80; P≥ 0.0002) compared with chemotherapy alone (5). As a result, the U.S. Food and Drug Administration (FDA) approved nivolumab in combination with chemotherapy in April 2021 as the first-line treatment for metastatic gastric cancer and esophageal adenocarcinoma. A recent study showed that the combination of sintilimab plus chemotherapy improved the OS and PFS regardless of PD-L1 expression status (15.2 vs.12.3 months; HR: 0.766; P ≥ 0.009) (6). One of the hallmarks of immunotherapy is its long-term efficacy, making it desirable to identify non-responders.
Several biomarkers such as PD-L1 expression (7), tumor mutation burden(TMB) (8) and microsatellite instability (MSI) have been considered to be potential predictors of survival outcomes (9). Unfortunately, the prognostic value of baseline biomarkers remains unclear. Currently, evidence from previous studies has linked inflammation to the proliferation, survival, and migration of tumor cells (10, 11). The causal link between inflammation and cancer is now well demonstrated (12, 13). The significance of inflammatory markers in predicting the outcome of patients who receive immune checkpoint inhibitors has been investigated (14). Inflammatory markers, such as neutrophil-to-lymphocyte ratio (NLR), monocyte-to-lymphocyte ratio (MLR), platelet-to-lymphocyte ratio (PLR), systemic inflammation index (SII), and derived neutrophil-to-lymphocyte ratio (dNLR), are potential predictors of immunotherapy efficacy in different cancers (15–17), suggesting that their analogies may have broad clinical applications. However, few studies have explored the function of inflammatory markers in patients with advanced gastric cancers receiving immunotherapy combined with chemotherapy, particularly those receiving the combination as first line treatment.
In this study, we explored the ability of inflammatory markers to predict the efficacy of immune checkpoint inhibitors combined with chemotherapy as first-line therapy for patients with advanced gastric cancer. The association between the inflammatory markers and survival was examined in a clinical trial cohort. The results were validated in an independent, real-world cohort, with the aim of identifying potential prognostic markers.
Methods
Study design and patients
This retrospective study enrolled patients diagnosed with advanced or metastatic gastric or gastro-esophageal junction cancer at the Medical Oncology Department of the First Affiliated Hospital of Zhejiang University. The inclusion criteria were as follows: histologically proven gastric adenocarcinoma; stage III or IV; received no previous systemic treatment or received prior neoadjuvant/adjuvant therapy if completed ≥6 months; at least six cycles of combined therapy and one treatment response evaluation; Eastern Cooperative Oncology Group (ECOG) PS ≤ 2. The exclusion criteria were as follows: pre-treatment blood count values were not obtained two weeks before the treatment initiation; did not receive immunotherapy as the initial therapy; double primary cancers; recent operation; infectious diseases; missing medical records of the first cycle; missing data on blood count. All patients received immune checkpoint inhibitors combined with chemotherapy as first-line treatment. All included patients with recurrence underwent R0 resection previously. The chemotherapy regimens were as follows: oxaliplatin plus capecitabine (XELOX), S-1 plus paclitaxel (SPA), oxaliplatin plus fluorouracil and leucovorin (FOLFOX) and S-1 plus oxaliplatin (SOX). The choice of combined regimen and dosage was based on the actual condition and preference of patients.
The clinical trial cohort comprised 45 patients from 5 clinical trials conducted in the Medical Oncology Department of the First Affiliated Hospital of Zhejiang University. The treatment was initiated from December 2017 to December 2020. Part of these clinical trials had previously been reported (18–21). The real-world cohort included 55 patients from the Medical Oncology Department. The treatment was initiated from March 2018 to June 2021. The study was approved by the Ethics Committee of Zhejiang University (reference number: 2022–375).
Data collection
Clinicopathological characteristics and follow-up status were collected. All laboratory values were measured two weeks before treatment initiation. Data were collected from the electronic medical records system. Fasting venous blood was collected in the early morning and analyzed. Staging evaluation was based on the eighth edition of TMN staging published by the International Cancer Control Alliance. Computed tomography (CT) and/or magnetic resonance imaging (MRI) were performed at baseline and every 2 or 3 cycles. Clinical response was classified as complete remission (CR), partial remission (PR), stable disease (SD), and progressive disease (PD), according to the Response Evaluation Criteria in Solid Tumors (RECIST [version 1.0]). Human epidermal growth factor receptor-2 (HER-2) was defined as positive if the IHC score was 3+ or if fluorescence in situ hybridization (FISH) was positive. NLR, MLR, PLR, SII and dNLR were calculated using the formula: neutrophils/lymphocytes, monocytes/lymphocytes, platelets/lymphocytes, neutrophils*platelets/lymphocytes, and neutrophils/(leukocytes-neutrophils), respectively.
Statistical analysis
Baseline characteristics of patients were summarized using descriptive frequencies and percentages, and categorical variables were analyzed using the Chi-square test or Fisher’s exact test. P value < 0.05 indicated statistically significant differences. Receiver operating characteristics (ROC) curve analysis was performed to determine the optimal cutoff value for each parameter. Survival curves were estimated using Kaplan-Meier analysis and differences were compared using log-rank test. The median estimated follow-up was calculated using the reverse Kaplan-Meier method, while univariate and multivariate Cox regression analyses were conducted to identify independent predictors of PFS and OS. Factors significantly associated with the PFS and OS in the univariable analysis were included in the multivariate analysis based on the stepwise forward procedure with enter and remove limits of 0.05 and 0.10, respectively. OS was defined as the time between the start of combined therapy and death or the last follow-up, while PFS was defined as the time between the start of combined therapy and disease progression or death. Statistical analyses were conducted on GraphPad Prism 9.0 (GraphPad Software, La Jolla, CA, USA), R language (R Core Team) and SPSS 26.0 (IBM Corp., Armonk, NY, USA).
Results
Characteristics of patients (clinical trial cohort)
A total of 45 patients were enrolled in the clinical trial cohort and their baseline characteristics are shown in Table 1. The age of the patients ranged from 37 to 74 years, with a median age of 64 years. Among them, 35 (78%) patients were male, 35 (78%) patients were ECOG PS 0, and 9 (20%) patients had cancer of GEJ. Notably, 8 (18%) of the patients had stage III whereas 37 (82%) had stage IV. In addition, 39 (100%, 39 of 39) patients were HER2-negative, while the HER2 status of the remaining patients was undetermined. Moreover, 44 (98%) patients were treated with capecitabine and oxaliplatin (XELOX) and only 1(2%) patient was treated with oxaliplatin plus fluorouracil and leucovorin (FOLFOX). Overall, 44 (98%) patients received an anti-PD-1 antibody treatment and only 1(2%) patient received an anti-PD-L1 antibody treatment (Supplementary Table S1).
Table 1 Clinical characteristics of the clinical trial and real-world cohort.
Efficiency (clinical trial cohort)
At the cutoff date of August 1, 2021, the median estimated follow-up time was 27.3 (95% CI 25.9-28.7) months. The median PFS and OS were 10.0 (95% CI 26.2-13.7) months and 17.7 (95% CI 29.4-26.0) months (Supplementary Figures S1A, B), respectively. There were 8 (17.7%) cases of CR, 25 (55.5%) cases of PR, 11 (24.4%) cases of SD, and 1 (2.2%) case of PD among the 45 patients. The overall response rate (ORR) was 73.3% and the disease control rate (DCR) was 97.7%. The 1-year survival rate was 62.2% (Supplementary Table S2).
Prognostic significance of inflammatory markers (clinical trial cohort)
The area under the ROC curve (AUC) was 0.683 for NLR, 0.660 for MLR, 0.558 for PLR, 0.662 for SII and 0.697 for dNLR (Supplementary Figure S2). Based on the cut-off value of inflammatory markers obtained from the ROC curves, the patients were divided into NLR-high (≥3.85) and NLR-low (<3.85); MLR-high (≥0.35) and MLR-low (<0.35); PLR-high (≥214.08) and PLR-low (<214.08); SII-high (≥1154.67) and SII-low (<1154.67); dNLR-high (≥2.45) and dNLR-low (<2.45) groups. Figure 1 shows the survival curves grouped according to levels of inflammatory markers. Compared with patients with high levels of inflammatory markers, patients with low levels of inflammatory markers had a longer median PFS when divided by NLR (12.7 vs. 7.8 months; HR: 0.40, 95% CI 0.18–0.90; P= 0.004; Figure 1A), MLR (12.8 vs. 7.9 months; HR: 0.42, 95% CI 0.21–0.82; P= 0.005; Figure 1C), PLR (12.6 vs. 8.3 months; HR: 0.47, 95% CI 0.19–1.11; P= 0.026; Figure 1E), SII (11.7 vs. 7.9 months; HR: 0.45, 95% CI 0.17–1.18; P= 0.029; Figure 1G). Median PFS time was only comparable between low-dNLR group and high-dNLR group (12.6 vs. 7.8 months; HR: 0.53, 95% CI 0.26–1.11; P= 0.056; Figure 1I). There was no significant difference in OS among groups separated by MLR (NR vs. 13.3 months; HR: 0.48, 95% CI 0.22–1.04; P= 0.059; Figure 1D), PLR (22.1 vs. 13.8 months; HR: 0.61, 95% CI 0.24–1.56; P= 0.233; Figure 1F), SII (20.7 vs.14.1 months; HR: 0.74, 95% CI 0.28–2.01; P= 0.522; Figure 1H), and dNLR (22.1 vs. 13.8 months; HR: 0.54, 95% CI 0.23–1.23; P= 0.107; Figure 1J). Remarkably, lower NLR predicted a better OS (23.8 vs. 13.0 months; HR: 0.39, 95% CI 0.16–0.94; P= 0.011; Figure 1B). We also observed that NLR was still significantly associated with PFS (17.9 vs. 10.6 vs. 7.8 months; P= 0.005; Supplementary Figure S3A) and OS (NR vs. 20.7 vs. 13.0 months; P= 0.024; Supplementary Figure S3B) when patients were equally divided into three groups.
Figure 1 Kaplan–Meier survival curves in the clinical trial cohort stratified by inflammatory markers for (A) PFS for NLR cut-off, (B) OS for NLR cut-off, (C) PFS for MLR cut-off, (D) OS for MLR cut-off, (E) PFS for PLR cut-off, (F) OS for PLR cut-off, (G) PFS for SII cut-off, (H) OS for SII cut-off, (I) PFS for dNLR cut-off and (J) OS for dNLR cut-off. The p values were calculated using the log-rank test (two-sided). CI, confidence interval; dNLR, derived neutrophil-to-lymphocyte ratio; MLR, monocyte-to-lymphocyte ratio; NLR, neutrophil-to-lymphocyte ratio; OS, overall survival; PLR, platelet-to-lymphocyte ratio; PFS, progression-free survival; SII, systemic immune-inflammation index.
NLR predicts outcomes in advanced gastric cancer patients undergoing immune checkpoint inhibitors combined with chemotherapy (clinical trial cohort)
Results of the univariate and multivariate proportional hazard analyses performed between baseline clinicopathological characteristics and survival in the clinical trial cohort are summarized in Table 2. Univariate predictors of PFS were age (HR: 0.48, 95% CI 0.24–0.95; P=0.036), ECOG PS (HR: 2.55, 95% CI 1.20–5.44; P=0.015), NLR (HR: 2.77, 95% CI 1.35–5.69; P=0.005), MLR (HR: 2.64, 95% CI 1.30–5.37; P=0.007), PLR (HR: 2.30, 95% CI 1.08–4.86; P=0.03) and SII (HR: 2.34, 95% CI 1.07–5.14; P=0.034), while ECOG PS (HR: 2.39, 95% CI 1.03–5.51; P=0.042) and NLR (HR: 2.59, 95% CI 1.20–5.61; P=0.016) were identified as independent predictors of PFS in the multivariate analysis. Similarly, univariate proportional hazard analyses revealed that NLR (HR: 2.66, 95% CI 1.21–5.82; P=0.015) was associated with OS and we found that NLR (HR: 3.35, 95% CI 1.42–7.91; P=0.006) along with ECOG PS (HR: 2.52, 95% CI 1.00–6.32; P=0.049) were independent predictors of OS (Table 2). Based on the prognostic parameters in the clinical trial cohort, we created a nomogram for predicting 1-year, 2-year, and median overall survival, the nomogram yielded an averaged concordance index (C-index) of 0.609 (95% CI, 0.491–0.727; Supplementary Figure S4).
Table 2 Univariate and multivariate analyses of the association between baseline characteristics and survival in the clinical trial cohort.
In addition, we examined the association between NLR and adverse events. Adverse events related to first-line treatment in the clinical trial cohort are listed in Supplementary Table S3. All 45(100%) patients experienced at least one adverse event and 31(68.9%) patients experienced grade 3 or higher treatment-related adverse effects. However, NLR-high was not associated with an increased incidence of high-grade adverse events (P = 0.519, chi-square test).
Characteristics of patients (real-world cohort)
We then validated the results obtained from the clinical cohort in an independent, real-world cohort of 55 patients. Of the 126 patients who had initially been recruited, 72 patients were excluded due to short treatment duration (n=47), recent operation(n=3), double primary cancer (n=4), immunotherapy not applied in the first cycle (n=2), and pre-treatment blood count not measured in 2 weeks(n=15) (Supplementary Figure S5). The baseline characteristics of patients are presented in Table 1. The age of the patients ranged from 32 to 81 years, with a median age of 65 years. 42 (76%) patients were male, 25 (45%) patients had an ECOG PS of 0, 25 (45%) patients had an ECOG PS of 1 and 5 (9%) patients had an ECOG PS of 2. The proportions of patients with stage III and stage IV disease were 7% and 93%, respectively. Moreover, 5 (9%) of the patients had GEJ cancer whereas 40 (95%, 40 of 42) patients were HER-2-negative. All patients received anti-PD-1 antibodies. The immunotherapy and chemotherapy regimens administered are presented (Supplementary Table S1). During the follow-up period, 30 patients (79%, 30 of 38) received subsequent treatment after they had disease progression while receiving first-line treatment. 18 (60%, 18 of 30) patients received targeted therapy, no patients received radiotherapy. The details of the treatment regimen are shown in Supplementary Table S4.
Efficiency (real-world cohort)
At the data cutoff date of February 1, 2022, the median estimated follow-up time was 15.3 (95%CI 11.4–19.2) months. Median PFS was 8.6 (95%CI 6.1–11.1) months and median OS was 18.2 (95%CI 17.1–19.4) months (Supplementary Figures S1C, D). There were 3 (5.5%) cases of CR, 27 (49.1%) cases of PR, 17 (30.9%) cases of SD and 8 (14.5%) cases of PD in 55 patients. The ORR was 54.5%, and the DCR was 85.5%. The 1-year survival rate was 54.5% (Supplementary Table S2).
Validation of the prognostic significance of NLR (real-world cohort)
Patients were divided into groups based on the same cut-off values used for the clinical trial cohort. A trend of superior PFS and OS benefit was consistently observed in NLR-low group compared with NLR-high group (10.8 vs. 6.5 months; HR: 0.46, 95% CI 0.24–0.88; P= 0.014; NR vs. 17.8 months; HR: 0.35, 95% CI 0.14–0.83; P= 0.022; Figures 2A, B). Additionally, we categorized patients into three groups equally and saw a similar trend in PFS (NR vs. 6.8 vs. 5.8 months; P= 0.016; Supplementary Figure S6A) and OS (18.5 vs. NR vs. 18.2 months; P= 0.08; Supplementary Figure S6B). Univariate proportional hazard analysis revealed that NLR, MLR and PLR were associated with PFS and OS. However, only high NLR (HR: 2.67, 95%CI 1.35–5.27; P= 0.005; HR: 3.69, 95% CI 1.40–9.11; P= 0.008) was found to be an independent predictor of poor outcomes in multivariate analysis (Supplementary Table S5). In addition, we validated our nomogram model with the real-world cohort, and the C-index was 0.669 (95% CI, 0.522–0.816), indicating good discrimination.
Figure 2 Kaplan-Meier survival curves in the real-world cohort stratified by NLR for (A) PFS for NLR cut-off and (B) OS for NLR cut-off. CI, confidence interval; NLR, neutrophil-to-lymphocyte ratio; OS, overall survival; PFS, progression-free survival.
Validation of the prognostic significance of NLR (pooled cohort)
The two cohorts were pooled to form one cohort for further analysis. Patients in the high-NLR group (n=41) had a shorter PFS than those in the low-NLR group (n=59) (7.0 vs. 12.7 months; HR: 2.30, 95% CI 1.40–3.78; P< 0.001; Figure 3A). Likewise, the high-NLR group had significantly shorter OS compared with those of the low-NLR group (13.8 vs. 32.6 months; HR: 2.50, 95% CI 1.36–4.60; P= 0.001; Figure 3B), with the 1-year OS rates for patients with low NLR and high NLR being 62.7% and 51.2%, respectively (Supplementary Table S6); These findings remained significant when we divided the pooled cohort equally into three groups according to NLR with respect to PFS (17.9 vs. 10.0 vs. 9.2 months; P= 0.002; Supplementary Figure S7A) and OS (32.6 vs. 20.7 vs. 13.0 months; P= 0.005; Supplementary Figure S7B). Results of Cox proportional hazard analysis confirm that NLR was an independent prognostic factor for PFS (HR: 2.75, 95% CI 1.61–4.71; P<0.001) and OS (HR: 3.25, 95% CI = 1.76–6.00; P<0.001) and validated to be an independent prognostic factor in multivariate analysis (Supplementary Table S7).
Figure 3 Kaplan-Meier survival curves in the pooled cohort stratified by NLR for (A) PFS for NLR cut-off and (B) OS for NLR cut-off. CI, confidence interval; NLR, neutrophil-to-lymphocyte ratio; OS, overall survival; PFS, progression-free survival.
Results of an exploratory analysis showed that the low-NLR group had longer PFS compared with the high-NLR group in most subgroups and significant improvement in PFS was achieved in subgroups irrespective of age, status of liver metastasis, history of smoke, and history of alcohol (all P<0.05; Figure 4). Among patients receiving platinum-based chemotherapy, those with low NLR had a better PFS (HR: 2.82, 95% CI 1.66–4.78; P<0.001). Furthermore, a trend of improvement was observed in PFS in other subgroups, although statistical significance was not achieved.
Figure 4 Forest plot of HRs for PFS based on the pooled cohort stratified by NLR cut-off. ECOG PS, Eastern Cooperative Oncology Group Performance Status; NLR, neutrophil-to-lymphocyte ratio.
Discussion
In the present study, we explored the role of inflammatory markers using a clinical trial cohort and validated the findings in a real-world cohort. Our principal finding was that NLR was the only independent inflammatory prognostic biomarker that showed a substantial effect on PFS and OS. Subgroup analysis in the pooled cohort based on age, liver metastasis, history of smoke and history of alcohol intake suggested that low NLR significantly prolonged PFS. To our knowledge, this is the first study to comprehensively assess the role of inflammatory markers in predicting the prognosis of previously untreated advanced gastric cancer patients receiving immune checkpoint inhibitors combined with chemotherapy.
More recent evidence has shown that inflammatory markers can predict short-term efficacy of immunotherapy in advanced gastric cancer patients. A study comprising 37 patients with advanced gastric cancer treated with first-line immunotherapy showed that PLR was an independent predictor of the OS but not the PFS (22). The baseline and early changes of MLR have been shown to influence survival outcomes in advanced gastric cancer on different lines (23). In our study, baseline MLR and PLR were associated with PFS, but not with OS. This discrepancy with previous reports may be attributed to confounding arising from the variety of lines and part of patients who received monotherapy. Remarkably, our study demonstrated that NLR was an independent prognostic factor for PFS and OS. Our results are consistent with those of previous studies, which demonstrate that NLR can predict the prognosis of several types of tumors (24). The relationship between elevated NLR and poor outcomes is supported by an umbrella review of 204 systematic reviews and meta-analyses from 86 studies (25). Several studies have recently demonstrated that NLR is an independent prognostic factor in patients with gastric or gastroesophageal junction cancer treated with nivolumab monotherapy (26–28). It has also been reported that the combination of NLR and TMB provides additional predictive value in patients treated with immunotherapy (29). The optimal cut-off of this research was defined as 3.85 for NLR by ROC analysis by nine-month progressive-free survival, which ranged from 2.5 to 4 reported in other studies (30–32). Given that the cut-off values of inflammatory markers are controversial, and our research provides a reference for future research. Interestingly, we found no significant association between NLR variations and ORR. It has been reported that NLR is not associated with ORR and DCR in patients receiving immunotherapy (33). Similarly, there was no statistical difference in ORR and DCR between low NLR and high NLR groups in 137 patients with metastatic gastric cancer treated with immunotherapy (34). A trend was found toward a higher CR rate in the NLR-low group (15.3% vs. 4.9%) and it required further investigation with larger sample sizes.
Of particular interest is the underlying basis of the relationship between NLR and outcomes. NLR characterizes the inflammatory response to cancer and reflects the disease burden. Neutrophils measured by NLR have been directly correlated with the intratumor neutrophil population (35). Tumor-activated neutrophils impair antitumor immunity and contribute to tumor progression via the GM-CSF-PD-L1 pathway (36) and engage in the metastatic process during cancer cell dissemination (37). Neutrophils are the primary source of metalloproteinase-9 (MMP-9), which promotes the release of vascular epithelial growth factor (VEGF) to create the tumor vasculature (38). Moreover, an elevated NLR is closely related to elevated circulating concentrations of inflammatory cytokines leading to a transition of the tumor microenvironment favorable for tumor invasion (39). Meanwhile, neutrophils have found to be associated with the myeloid-derived suppressor cells (MDSC) (40), which is associated with advanced status and metastases of various solid tumors (41). This may partly explain why high NLR always reflects a more advanced disease with potentially more aggressive tumors and is a potential prognostic factor for poor outcomes for patients with advanced gastric cancers (39). Cancer-triggered Immune response also relies on lymphocytes. Zhang et al. concluded that a high level of tumor-infiltrating lymphocytes (TIL) correlated with a low rate of metastasis and better survival in gastric cancer (42). The densities of CD3 (+), CD8 (+), and CD45RO (+) TILs were associated with lymph node metastasis and survival time (43). In a meta-analysis of 33 studies including 2559 patients, CD8+ TIL was an essential biomarker for predicting the efficacy of ICI in different cancers, regardless of monotherapy or combination with chemotherapy (44). Immune checkpoint inhibitors have been shown to improve outcomes of patients with advanced tumors, especially those infiltrated by CD8+T cells (45). Chemotherapeutics which induce immunogenicity (e.g., oxaliplatin, cyclophosphamide) can also provide additional or synergistic effects when used in combination with immune checkpoint inhibitors (46). High NLR indicates relatively depleted lymphocytes, leading to a weakened immune response to malignant cells (47, 48). These reasons may explain the unique prognostic value of NLR in patients treated with immune checkpoint inhibitors combined with chemotherapy. dNLR was calculated using the formulas: neutrophils/(leukocytes-neutrophils). Thus it does not reflect the level of lymphocytes well, which may be partially responsible for its ineffectiveness of prognostic value in advanced gastric cancer.
The exploration of prognostic markers based on clinical trials followed by validation in real-world settings provides reliable results with good consistency. Cuzick et al. developed a prognostic model using IHC markers in patients from the tamoxifen and anastrozole arms of the ATAC trial and validated their findings in an independent cohort in the real world (49). At present, most studies on inflammatory factors in gastric cancer treated with immunotherapy are based on single cohorts. Little focus has been paid to the identification of the function of MLR in patients using real-world cohorts (22). Based on results obtained from the clinical trial cohort, we concluded that NLR was an independent prognostic factor, a finding that was validated in the real-world cohort. Moreover, similar results were also found in the subgroup analysis in the pooled cohort. Therefore, the conclusions derived from this analysis are reliable.
However, our study had several limitations. First, this was a retrospective study involving patients from one study center. Second, the sample size of this study was small and data on the molecular characteristics of patients, such as major mismatch repair and PD-L1 expression, were insufficient. Therefore, it is difficult to draw a conclusion on the prognostic superiority NLR over the molecular indicators. Third, since the application time of combination therapy in the real world in China is relatively short, the median follow-up time in the real-world cohort is shorter than in the clinical trial cohort. Despite its limitations, this study demonstrates the potential of inflammatory markers to predict outcomes of patients with advanced gastric cancer treated with chemotherapy plus immunotherapy as first-line treatment. Future multicenter investigations are necessary to validate the results drawn from this research.
Conclusion
In summary, we found that NLR can predict PFS and OS in patients with advanced gastric cancers who received first-line treatment of immunotherapy combined with chemotherapy. Therefore, NLR may become an inexpensive, usable, and reliable biomarker for predicting outcomes of patients with advanced gastric cancer in this setting. Further prospective studies should explore this possibility.
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics statement
The studies involving human participants were reviewed and approved by Ethics Committee of Zhejiang University (reference number: 2022–375). Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.
Author contributions
MW and YD: data acquisition and analysis, writing. NL, XM, CX, JQ, HJ, YZ, and LW: data acquisition. YD and CM: review and editing. LT and NX: conceptualization, funding acquisition, review and editing. All authors read and approved the final manuscript.
Funding
This work was supported by grants from National Health and Family Planning Commission Research Fund & Zhejiang Provincial Medical and Health Major Science and Technology Plan Project (No: KWJ-ZJ-1802).
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.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fonc.2022.1029960/full#supplementary-material
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Keywords: neutrophil-to-lymphocyte ratio, immune checkpoint inhibitor, inflammatory markers, gastric cancer, prognosis
Citation: Wan M, Ding Y, Mao C, Ma X, Li N, Xiao C, Qian J, Jiang H, Zheng Y, Wu L, Teng L and Xu N (2022) Association of inflammatory markers with survival in patients with advanced gastric cancer treated with immune checkpoint inhibitors combined with chemotherapy as first line treatment. Front. Oncol. 12:1029960. doi: 10.3389/fonc.2022.1029960
Received: 28 August 2022; Accepted: 17 October 2022;
Published: 28 October 2022.
Edited by:
Xiaofei Shen, Nanjing Drum Tower Hospital, ChinaReviewed by:
Guozhi Wu, Lanzhou University Medical College, ChinaPengfei Yu, Cancer Research Institute, China
Shiva Basnet, Southern University of Science and Technology, China
Copyright © 2022 Wan, Ding, Mao, Ma, Li, Xiao, Qian, Jiang, Zheng, Wu, Teng and Xu. 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: Nong Xu, bm9uZ3h1QHpqdS5lZHUuY24=
†These authors have contributed equally to this work and share first authorship