Li Tao, Liu Tingting, Zhao Lei, Liu Lu, Zheng Xuan, Wang Jinliang, Zhang Fan, Hu Yi
Graduate School, Medical School of Chinese People's Liberation Army (PLA), Beijing, China.
Department of Oncology, The First Medical Center, Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.
Front Oncol. 2023 Jan 5;12:976078. doi: 10.3389/fonc.2022.976078. eCollection 2022.
Gastric cancer (GC) is one of the most frequently diagnosed cancers and one of the leading causes of cancer deaths worldwide, especially in eastern Asia and China. Anti-PD-1 immune checkpoint inhibitors, Pembrolizumab and Nivolumab, have been approved for the treatment of locally advanced or metastatic gastric or gastroesophageal junction cancer (GC/GEJC). Our study evaluated the effectiveness and safety of anti-PD-1-based treatment (monotherapy or combination therapy) in Chinese patients with advanced or metastatic GC/GEJCs in a real-world setting.
A retrospective cohort study was conducted, and 54 patients from May 31, 2015, to May 31, 2021, were included in our analysis, including 19 patients treated with anti-PD-1 monotherapy and 35 patients treated with anti-PD-1 combination therapy. Demographic and clinical information were evaluated. Clinical response, survival outcomes, and safety profile were measured and analyzed.
Overall, the median overall survival (mOS) was 11.10 months (95% CI, 7.05-15.15), and the median progression-free survival (mPFS) was 3.93 months (95% CI, 2.47-5.39). Of the patients, 16.7% achieved a clinical response, and 72.2% achieved disease control. Prolonged overall survival (OS) and progression-free survival (PFS) and increased clinical response were observed in the combination group compared with the monotherapy group, although statistical significance was not reached. In subgroups with live metastases or elevated baseline neutrophil-to-lymphocyte ratio (NLR) levels, combination therapy outperformed anti-PD-1 alone in survival outcomes. Patients treated with anti-PD-1 monotherapy (n = 5, 26.3%) had fewer treatment-related adverse events (TRAEs) than those in the combination group (n = 22, 62.9%). There were also fewer patients with TRAEs of grades 3-5 with monotherapy (n = 2, 10.5%) than with combination therapy (n = 7, 20.0%). Pneumonitis in three patients was the only potential immune-related adverse event reported.
Anti-PD-1-based monotherapy and combination therapy showed favorable survival outcomes and manageable safety profiles in advanced or metastatic GC/GEJCs. In clinical treatment, immunotherapy should be an indispensable choice in the treatment strategy for GC/GEJC. Patients with a heavy tumor burden and more metastatic sites might benefit more from combination therapy. Elderly patients and patients with more treatment lines or high Eastern Cooperative Oncology Group (ECOG) performance scores might be more suitable for immune monotherapy, and some clinical benefits have been observed.
胃癌(GC)是最常被诊断出的癌症之一,也是全球癌症死亡的主要原因之一,尤其是在东亚和中国。抗程序性死亡蛋白1(PD-1)免疫检查点抑制剂帕博利珠单抗和纳武利尤单抗已被批准用于治疗局部晚期或转移性胃癌或胃食管交界癌(GC/GEJC)。我们的研究评估了在真实世界中,基于抗PD-1的治疗(单药治疗或联合治疗)对中国晚期或转移性GC/GEJC患者的有效性和安全性。
进行了一项回顾性队列研究,纳入了2015年5月31日至2021年5月31日期间的54例患者,其中19例接受抗PD-1单药治疗,35例接受抗PD-1联合治疗。评估了人口统计学和临床信息。测量并分析了临床反应、生存结果和安全性。
总体而言,中位总生存期(mOS)为11.10个月(95%置信区间,7.05-15.15),中位无进展生存期(mPFS)为3.93个月(95%置信区间,2.47-5.39)。患者中,16.7%获得了临床反应,72.2%实现了疾病控制。与单药治疗组相比,联合治疗组观察到总生存期(OS)和无进展生存期(PFS)延长以及临床反应增加,尽管未达到统计学显著性。在有肝转移或基线中性粒细胞与淋巴细胞比值(NLR)水平升高的亚组中,联合治疗在生存结果方面优于单独使用抗PD-1治疗。接受抗PD-1单药治疗的患者(n = 5,26.3%)比联合治疗组(n = 22,62.9%)的治疗相关不良事件(TRAEs)更少。单药治疗的3-5级TRAEs患者(n = 2,10.5%)也比联合治疗组(n = 7,20.0%)更少。3例患者发生肺炎是唯一报告的潜在免疫相关不良事件。
基于抗PD-1的单药治疗和联合治疗在晚期或转移性GC/GEJC中显示出良好的生存结果和可控的安全性。在临床治疗中,免疫治疗应成为GC/GEJC治疗策略中不可或缺的选择。肿瘤负荷重和转移部位多的患者可能从联合治疗中获益更多。老年患者以及治疗线数更多或东部肿瘤协作组(ECOG)体能状态评分高的患者可能更适合免疫单药治疗,并且已观察到一些临床益处。