Tian Yuan, Zhao Qun, Li Yong, Fan Liqiao, Zhang Zhidong, Zhao Xuefeng, Tan Bibo, Wang Dong, Yang Peigang
Department of General Surgery, The Fourth Affiliated Hospital, Hebei Medical University, No.12, Jian-Kang Road, Shijiazhuang 050019, China.
Gastroenterol Res Pract. 2021 Jul 22;2021:5590626. doi: 10.1155/2021/5590626. eCollection 2021.
This paper is aimed at comparing the short-term efficacy of the combination of docetaxel, oxaliplatin, and capecitabine (DOX) with the combination of oxaliplatin and capecitabine (XELOX) as neoadjuvant chemotherapy regimens for the treatment of patients with resectable gastric or gastroesophageal junction adenocarcinoma.
A total of 300 patients aged 20-60 years with resectable gastric or gastroesophageal junction adenocarcinoma who were evaluated with cT3/4Nany were randomly assigned into 3 groups: DOX group ( = 100, treated with neoadjuvant DOX plus adjuvant XELOX), XELOX group ( = 100, treated with perioperative XELOX), and surgery group ( = 100, treated with adjuvant XELOX).
A total of 93, 92, and 95 patients were enrolled in the DOX, XELOX, and surgery groups, respectively. The pathological complete response (pCR) rate was 16.1% in the DOX group and 4.3% in the XELOX group ( = 0.008). There were 56 (61.3%) patients in the DOX group who presented with surgical complications, 22 (23.9%) patients in the XELOX group, and 37 (38.9%) patients in the surgery group. The most common grade 3-4 adverse events in these three groups were neutropenia (32.3%, 30.4%, and 21.1%), leucopenia (21.5%, 22.8%, and 15.8%), nausea (15.1%, 16.3%, and 12.6%), and fatigue (10.8%, 7.6%, and 8.4%).
Neoadjuvant DOX is an effective and feasible regimen and might represent an option for young and middle-aged patients with locally advanced, resectable gastric or gastroesophageal junction adenocarcinoma.
本文旨在比较多西他赛、奥沙利铂和卡培他滨联合方案(DOX)与奥沙利铂和卡培他滨联合方案(XELOX)作为新辅助化疗方案治疗可切除胃或胃食管交界腺癌患者的短期疗效。
总共300例年龄在20 - 60岁、经cT3/4Nany评估为可切除胃或胃食管交界腺癌的患者被随机分为3组:DOX组(n = 100,接受新辅助DOX加辅助XELOX治疗)、XELOX组(n = 100,接受围手术期XELOX治疗)和手术组(n = 100,接受辅助XELOX治疗)。
DOX组、XELOX组和手术组分别有93例、92例和95例患者入组。DOX组的病理完全缓解(pCR)率为16.1%,XELOX组为4.3%(P = 0.008)。DOX组有56例(61.3%)患者出现手术并发症,XELOX组有22例(23.9%),手术组有37例(38.9%)。这三组中最常见的3 - 4级不良事件为中性粒细胞减少(32.3%、30.4%和21.1%)、白细胞减少(21.5%、22.8%和15.8%)、恶心(15.1%、16.3%和12.6%)以及疲劳(10.8%、7.6%和8.4%)。
新辅助DOX是一种有效且可行的方案,可能是局部晚期、可切除胃或胃食管交界腺癌的中青年患者的一种选择。