Division of Abdominal Cancer, Department of Medical Oncology, Cancer Center and Laboratory of Molecular Targeted Therapy in Oncology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Front Immunol. 2024 Jun 12;15:1370860. doi: 10.3389/fimmu.2024.1370860. eCollection 2024.
Programmed cell death protein-1 (PD-1) inhibitor-based therapy has demonstrated promising results in metastatic gastric cancer (MGC). However, the previous researches are mostly clinical trials and have reached various conclusions. Our objective is to investigate the efficacy of PD-1 inhibitor-based treatment as first-line therapy for MGC, utilizing real-world data from China, and further analyze predictive biomarkers for efficacy.
This retrospective study comprised 105 patients diagnosed with MGC who underwent various PD-1 inhibitor-based treatments as first-line therapy at West China Hospital of Sichuan University from January 2018 to December 2022. Patient characteristics, treatment regimens, and tumor responses were extracted. We also conducted univariate and multivariate analyses to assess the relationship between clinical features and treatment outcomes. Additionally, we evaluated the predictive efficacy of several commonly used biomarkers for PD-1 inhibitor treatments.
Overall, after 28.0 months of follow-up among the 105 patients included in our study, the objective response rate (ORR) was 30.5%, and the disease control rate (DCR) was 89.5% post-treatment, with two individuals (1.9%) achieving complete response (CR). The median progression-free survival (mPFS) was 9.0 months, and the median overall survival (mOS) was 22.0 months. According to both univariate and multivariate analyses, favorable OS was associated with patients having Eastern Cooperative Oncology Group performance status (ECOG PS) of 0-1. Additionally, normal baseline levels of carcinoembryonic antigen (CEA), as well as the combination of PD-1 inhibitors with chemotherapy and trastuzumab in patients with human epidermal growth factor receptor 2 (HER2)-positive MGC, independently predicted longer PFS and OS. However, microsatellite instability/mismatch repair (MSI/MMR) status and Epstein-Barr virus (EBV) infection status were not significantly correlated with PFS or OS extension.
As the first-line treatment, PD-1 inhibitors, either as monotherapy or in combination therapy, are promising to prolong survival for patients with metastatic gastric cancer. Additionally, baseline level of CEA is a potential predictive biomarker for identifying patients mostly responsive to PD-1 inhibitors.
程序性死亡蛋白-1(PD-1)抑制剂为基础的治疗在转移性胃癌(MGC)中显示出了有希望的结果。然而,之前的研究大多是临床试验,得出了各种结论。我们的目的是利用来自中国的真实世界数据,研究 PD-1 抑制剂为基础的治疗作为 MGC 一线治疗的疗效,并进一步分析疗效的预测生物标志物。
本回顾性研究纳入了 2018 年 1 月至 2022 年 12 月期间在四川大学华西医院接受各种 PD-1 抑制剂为基础的治疗作为一线治疗的 105 例 MGC 患者。提取患者特征、治疗方案和肿瘤反应。我们还进行了单变量和多变量分析,以评估临床特征与治疗结果之间的关系。此外,我们评估了几种常用的 PD-1 抑制剂治疗预测生物标志物的预测疗效。
在我们研究的 105 例患者中,总体随访 28.0 个月后,治疗后的客观缓解率(ORR)为 30.5%,疾病控制率(DCR)为 89.5%,有 2 例(1.9%)患者达到完全缓解(CR)。中位无进展生存期(mPFS)为 9.0 个月,中位总生存期(mOS)为 22.0 个月。根据单变量和多变量分析,ECOG PS 为 0-1 的患者具有较好的 OS。此外,基线癌胚抗原(CEA)正常水平,以及 PD-1 抑制剂联合化疗和曲妥珠单抗用于人表皮生长因子受体 2(HER2)阳性 MGC 的患者,独立预测更长的 PFS 和 OS。然而,微卫星不稳定性/错配修复(MSI/MMR)状态和 EBV 感染状态与 PFS 或 OS 延长没有显著相关性。
作为一线治疗,PD-1 抑制剂单药或联合治疗,有望延长转移性胃癌患者的生存时间。此外,CEA 的基线水平是识别对 PD-1 抑制剂最有反应的患者的潜在预测生物标志物。