Department of Pharmacy, The First Hospital of China Medical University, Shenyang, Liaoning, PR China.
School of Pharmacy, China Medical University, Shenyang, Liaoning, PR China.
BMC Cancer. 2024 Oct 9;24(1):1249. doi: 10.1186/s12885-024-12998-w.
Immune checkpoint inhibitors (ICIs) have shown encouraging treatment efficacy for upper gastrointestinal cancers (UGICs). However, durable clinical responses only existed in a minority of patients. We evaluated evidence predicting survival benefits to identify the optimal population followed by ICI-based therapy.
A comprehensive search was performed using PubMed, Embase, Cochrane Library, and Web of Science to identify clinical trials for UGICs with ICI-based therapy. The outcomes were objective response rate (ORR), progression-free survival (PFS), and overall survival (OS). The quality of evidence was evaluated using the Grading of Recommendations Assessment, Development and Evaluation System (GRADE).
Thirty-six studies comprising 12,440 patients were included for quantitative synthesis. Patients with PD-L1-positive (OR = 2.08, p < 0.00001), EBV+ (OR = 8.47, p = 0.003) tumors were more likely to respond to ICI treatment. Moreover, OS was significantly improved with the statistical subgroup difference concerning sex (p = 0.02) and region (p = 0.02). An exploratory subgroup analysis showed significantly improved OS with ICI plus chemotherapy in patients with CPS ≥ 10 (HR = 0.66, p = 0.001) and CPS ≥ 1 (HR = 0.75, p < 0.00001).
UGIC patients with PD-L1-positive, EBV + status are associated with a better therapeutic response to ICI-based therapy. The male patients and Asian patients could derive more survival benefits following ICI treatment than female and non-Asian ones. A combination of prognostic and predictive factors was suggested to help guide immunotherapy decision-making in UGIC patients.
免疫检查点抑制剂(ICIs)在治疗上消化道癌症(UGICs)方面显示出令人鼓舞的疗效。然而,持久的临床反应仅存在于少数患者中。我们评估了预测生存获益的证据,以确定接受 ICI 治疗的最佳人群。
使用 PubMed、Embase、Cochrane 图书馆和 Web of Science 全面检索了接受 ICI 治疗的 UGIC 临床试验。结果为客观缓解率(ORR)、无进展生存期(PFS)和总生存期(OS)。使用推荐评估、制定与评估系统(GRADE)评估证据质量。
纳入 36 项研究共 12440 例患者进行定量合成。PD-L1 阳性(OR=2.08,p<0.00001)和 EBV+(OR=8.47,p=0.003)肿瘤患者对 ICI 治疗更有可能有反应。此外,关于性别(p=0.02)和地区(p=0.02)存在统计学亚组差异,OS 得到显著改善。探索性亚组分析显示,CPS≥10(HR=0.66,p=0.001)和 CPS≥1(HR=0.75,p<0.00001)的患者接受 ICI 联合化疗的 OS 显著改善。
PD-L1 阳性、EBV+状态的 UGIC 患者对 ICI 治疗的疗效更好。男性和亚洲患者接受 ICI 治疗比女性和非亚洲患者更能获得生存获益。建议联合预后和预测因素,以帮助指导 UGIC 患者的免疫治疗决策。