Zhan Zhouwei, Chen Bijuan, Xu Shaohua, Lin Ruyu, Chen Haiting, Ma Xiaohuan, Lin Xuanping, Huang Wanting, Zhuo Changhua, Chen Yu, Guo Zengqing
Department of Medical Oncology, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, Fujian, China.
Department of Radiation Oncology, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, Fujian, China.
Front Immunol. 2025 Feb 4;16:1518217. doi: 10.3389/fimmu.2025.1518217. eCollection 2025.
Although immune checkpoint inhibitors (ICIs) and anti-angiogenic drugs have demonstrated effectiveness in treating advanced gastric cancer (GC), their role in neoadjuvant or conversion therapy remains uncertain. This study aimed to evaluate the efficacy and safety of combining neoadjuvant chemotherapy with anti-angiogenesis and ICIs in patients with locally advanced GC (LAGC).
In this cohort study, we reviewed our prospectively maintained GC database and included individuals diagnosed with clinical stage II-III GC who received neoadjuvant therapy followed by surgery between January 2022 and August 2023. The treatment protocol combined ICIs, anti-angiogenic therapy (specifically apatinib), and chemotherapy (S-1 with oxaliplatin). A systematic approach was used to document patients' clinical and pathological characteristics, pathological findings, and survival outcomes, which were subsequently analyzed in detail.
A total of 38 individuals met the study's inclusion criteria, with the majority (32 patients, 84.2%) having clinical stage III GC. All participants underwent surgery, resulting in a notable R0 resection rate of 97.4%. The rates of major pathological response (MPR) and pathological complete response (pCR) were 47.4% and 23.7%, respectively. Post-surgery, 36 patients (92.1%) received adjuvant chemotherapy. With a median follow-up of 22 months, ten patients experienced disease recurrence, including three who died from tumor relapse. The 1-year overall survival (OS) rate stood at 100%, and the disease-free survival (DFS) rate was 94.7%, with median OS and DFS yet to be reached. The neoadjuvant therapy regimen was generally well-tolerated, with no grade 5 treatment-related adverse events (TRAEs) reported. Only one patient experienced a grade 4 TRAE (immune-related hepatitis), while the most common grade 3 TRAEs included thrombocytopenia, elevated aminotransferase levels, and neutropenia.
The combination of neoadjuvant chemotherapy, anti-angiogenic therapy, and ICIs has proven effective in treating LAGC patients, achieving high pCR rates and favorable survival outcomes while maintaining an acceptable safety profile.
尽管免疫检查点抑制剂(ICIs)和抗血管生成药物已在晚期胃癌(GC)治疗中显示出疗效,但其在新辅助或转化治疗中的作用仍不确定。本研究旨在评估新辅助化疗联合抗血管生成药物和ICIs治疗局部晚期胃癌(LAGC)患者的疗效和安全性。
在这项队列研究中,我们回顾了前瞻性维护的GC数据库,纳入了2022年1月至2023年8月期间诊断为临床II-III期GC且接受新辅助治疗后行手术的患者。治疗方案包括ICIs、抗血管生成治疗(具体为阿帕替尼)和化疗(S-1联合奥沙利铂)。采用系统方法记录患者的临床和病理特征、病理结果及生存结局,并随后进行详细分析。
共有38例患者符合研究纳入标准,其中大多数(32例,84.2%)为临床III期GC。所有参与者均接受了手术,R0切除率高达97.4%。主要病理缓解(MPR)率和病理完全缓解(pCR)率分别为47.4%和23.7%。术后,36例患者(92.1%)接受了辅助化疗。中位随访22个月时,10例患者出现疾病复发,其中3例死于肿瘤复发。1年总生存(OS)率为100%,无病生存(DFS)率为94.7%,中位OS和DFS尚未达到。新辅助治疗方案总体耐受性良好,未报告5级治疗相关不良事件(TRAEs)。仅1例患者出现4级TRAE(免疫相关肝炎),最常见的3级TRAEs包括血小板减少、转氨酶水平升高和中性粒细胞减少。
新辅助化疗、抗血管生成治疗和ICIs联合应用已被证明在治疗LAGC患者方面有效,可实现高pCR率和良好的生存结局,同时保持可接受的安全性。