内科学
肿瘤科
顺铂
随机对照试验
临床研究阶段
临床终点
危险系数
养生
癌症
新辅助治疗
作者
Keijiro Sugimura,Hiroshi Miyata,Koji Tanaka,Tomoki Makino,Atsushi Takeno,Osamu Shiraishi,Masaaki Motoori,Makoto Yamasaki,Yutaka Kimura,Motohiro Hirao,Kazumasa Fujitani,Takushi Yasuda,Masaki Mori,Hidetoshi Eguchi,Masahiko Yano,Yuichiro Doki
出处
期刊:Annals of Surgery
[Ovid Technologies (Wolters Kluwer)]
日期:2021-12-01
卷期号:274 (6)
被引量:1
标识
DOI:10.1097/sla.0000000000004564
摘要
Objective We conducted a multicenter randomized prospective phase 2 trial of chemoradiotherapy (CRT) versus chemotherapy (CT) as initial induction therapy for conversion surgery (CS) in clinical T4b esophageal cancer. We compared treatment effects and adverse events. Summary background data Although induction followed by CS is potentially curative for T4b esophageal cancer, the optimal initial induction treatment is unclear. Methods Ninety-nine patients with T4b esophageal cancer were randomly allocated to chemoradiotherapy (Group A, n = 49) or CT (Group B, n = 50) as initial induction treatment. CRT consisted of radiation (50.4 Gy) with cisplatin and 5-fluorouracil. CT consisted of 2 cycles of docetaxel plus cisplatin and 5-fluorouracil (DCF). CRT or CT was followed by CS if resectable. If unresectable, the patient received the other treatment as secondary treatment. CS was performed if resectable after secondary treatment. The primary end point was 2-year overall survival. Results In Group A, CS was performed in 34 (69%) and 7 patients (14%) after initial and secondary treatment. In Group B, CS was performed in 25 (50%) and 17 patients (34%) after initial and secondary treatment. The R0 resection rate after initial and secondary treatment was similar (78% vs 76%, P = 1.000). Adverse events including leukopenia, neutropenia, febrile neutropenia, and diarrhea were significantly more frequent in Group B. Group A had better histological complete response of the primary tumor (40% vs 17%, P = 0.028) and histological nodal status (P = 0.038). Conclusions Upfront CRT was superior to upfront CT in terms of pathological effects and adverse events. The Japan Registry of Clinical Trials (s051180164).
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