Sun Chongyuan, Wang Tongbo, Zhang Xiaojie, Zhao Lulu, Niu Penghui, Wang Wanqing, Luan Xiaoyi, Han Xue, Chen Yingtai, Zhao Dongbing
Department of Pancreatic and Gastric Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Front Oncol. 2025 Jun 4;15:1539534. doi: 10.3389/fonc.2025.1539534. eCollection 2025.
Neoadjuvant chemotherapy increases the probability of achieving negative margins and may even lead to pathological complete response (pCR) in locally advanced gastric cancer (LAGC). The incorporation of neoadjuvant immunotherapy is promising in further enhancing the pCR rate. However, long-term survival outcomes and factors affecting the prognosis of pCR patients have not been fully elucidated.
We conducted a retrospective analysis of all patients who achieved pCR between January 2004 and June 2023. Cox regression models were used to identify clinicopathological predictors of overall survival (OS) and disease-free survival (DFS). Survival curves were plotted using the Kaplan-Meier method and compared using the log-rank test.
After screening, 112 patients were included in the study, with a median follow-up time of 42 (range: 2-117) months and a pCR rate of 7.4%. The 3- and 5-year OS rates were 90.2% and 83.3%, respectively, while the 3- and 5-year DFS rates were 86.8% and 82.0%, respectively. Within the multivariate Cox model, neoadjuvant chemotherapy was a prognostic factor for improved OS and DFS. There was no statistically significant disparity in OS and DFS between patients who received postoperative adjuvant therapy and those who did not. Moreover, the combination of neoadjuvant immunotherapy with chemotherapy, as compared to neoadjuvant chemotherapy alone, substantially increased the pCR rate (p <0.001).
Patients with LAGC who achieved pCR demonstrated favorable long-term survival outcomes, with no additional survival benefits conferred by adjuvant therapy. Although neoadjuvant immunotherapy increased the pCR rate, its impact on the prognosis of pCR patients requires further investigation.
新辅助化疗可提高局部晚期胃癌(LAGC)实现切缘阴性的概率,甚至可能导致病理完全缓解(pCR)。新辅助免疫治疗的加入有望进一步提高pCR率。然而,pCR患者的长期生存结果及影响预后的因素尚未完全阐明。
我们对2004年1月至2023年6月间所有达到pCR的患者进行了回顾性分析。采用Cox回归模型确定总生存(OS)和无病生存(DFS)的临床病理预测因素。使用Kaplan-Meier方法绘制生存曲线,并采用对数秩检验进行比较。
经过筛选,112例患者纳入研究,中位随访时间为42(范围:2 - 117)个月,pCR率为7.4%。3年和5年OS率分别为90.2%和83.3%,3年和5年DFS率分别为86.8%和82.0%。在多变量Cox模型中,新辅助化疗是OS和DFS改善的预后因素。接受术后辅助治疗和未接受术后辅助治疗的患者在OS和DFS方面无统计学显著差异。此外,与单纯新辅助化疗相比,新辅助免疫治疗联合化疗显著提高了pCR率(p <0.001)。
达到pCR的LAGC患者显示出良好的长期生存结果,辅助治疗未带来额外的生存益处。虽然新辅助免疫治疗提高了pCR率,但其对pCR患者预后的影响仍需进一步研究。