免疫疗法对晚期胃癌的疗效:一项多中心观察研究的初步结果

A. Rays, М. Y. Fedyanin, D. V. Popov, I. Pokataev, М. A. Lyadova, L. G. Zhukova, D. Stroyakovsky, М. V. Volkonsky, D. А. Gavrilova, N. Besova, А. Tryakin
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摘要

背景。由于PD-L1抗体在转移性胃癌(mGC)二线及后续治疗中的疗效较低,此类患者的最佳治疗策略和预测性生物标志物的适当选择仍具有挑战性。我们的研究旨在评估常规临床实践中免疫检查点抑制剂单药治疗 mGC 患者,尤其是重度治疗患者的疗效。我们回顾性分析了2018年至2023年期间在莫斯科5个肿瘤中心接受nivolumab或pembrolizumab治疗的晚期胃癌患者的数据。我们研究的主要终点是6个月的PFS。次要终点为总生存期(OS)、客观反应率(ORR)和疾病控制率(DCR)。毒性采用CTC AE v5.0量表进行评估。纳入了2018年1月1日至2023年2月28日期间接受免疫检查点抑制剂治疗的122例mGC患者。6个月的PFS率为31.6%。中位OS为7个月(95% CI:2-20),中位PFS为3个月(95% CI:1.5-9.5)。与 MSS 相比,MSI 患者的 OS 有明显的统计学差异(25 个月 vs 6 个月;95% CI:0,21 - 0,86;HR:0,43)。此外,还观察到 PFS 更高的趋势(MSI 为 10 个月,MSS 为 3 个月;95% CI:0,26 - 1,01;HR:0,51)。根据 PD-L1 CPS,MSS 患者的 PFS 和 OS 没有统计学意义。ORR和DCR分别为36.6%和10.6%。没有观察到假性进展或致命的免疫相关不良反应。我们的实际数据与已发表的文献和临床试验结果一致。需要进一步研究确定预后因素,并为接受 ICIs 的患者建立预后模型,以优化 mGC 的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of immunotherapy in advanced gastric cancer: preliminary results of a multicenter observational study
Background. Due to the low efficacy of PD-L1 antibodies in second and subsequent lines of metastatic gastric cancer (mGC), the optimal treatment strategy of such patients and appropriate choice of predictive biomarkers remain challenging. The aim of our study is to assess the efficacy of immune checkpoint inhibitors monotherapy in patients with mGC in routine clinical practice, especially in heavily-pretreated patients.Materials and methods. We retrospectively analyzed data of patients treated in five oncology centers in Moscow between 2018 and 2023, who received nivolumab or pembrolizumab for advanced gastric cancer. Primary end-point of our study was 6-months PFS. Secondary end-points were overall survival (OS), objective response rate (ORR), and disease control rate (DCR). Toxicity was assessed using CTC AE v5.0 scale.Results. 122 patients with mGC who received immune checkpoint inhibitors were included between 1 January 2018 and 28 February 2023. 6-months PFS rate was 31,6%. The median OS was 7 months (95% CI: 2-20), the median PFS was 3 months (95% CI: 1,5-9,5). A statistically significant difference in OS was detected in patients with MSI compared to MSS (25 months vs 6 months; 95% CI: 0,21 – 0,86; HR: 0,43). A trend towards higher PFS was observed as well (10 months in MSI vs 3 months in MSS; 95% CI:0,26 – 1,01; HR: 0,51). No statistical significance in PFS and OS according to PD-L1 CPS was found among patients with MSS. ORR and DCR were 36,6% and 10,6%, respectively. No cases of pseudoprogression or fatal immune-related AEs were observed.Conclusion. Our real-world data is consistent with published literature and the results from clinical trials. Further studies are needed to determine prognostic factors and to establish prognostic model of patients receiving ICIs for optimal treatment strategy of mGC.
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