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研究方案:局部软组织肉瘤新辅助化疗和辅助化疗对比直接手术及辅助化疗的随机III期试验:日本临床肿瘤学会研究JCOG2102(NACLESS)

Study protocol: randomized phase III trial of neo-adjuvant and adjuvant chemotherapy vs. immediate surgery and adjuvant chemotherapy for localized soft tissue sarcoma: Japan Clinical Oncology Group study JCOG2102 (NACLESS).

作者信息

Funauchi Yuki, Tsukushi Satoshi, Hiraga Hiroaki, Sakamoto Akio, Kunisada Toshiyuki, Nagano Akihito, Hiraoka Koji, Kikuta Kazutaka, Yonemoto Tsukasa, Ae Keisuke, Kawai Akira, Endo Makoto, Sano Yusuke, Machida Ryunosuke, Sekita Tetsuya, Fukuda Haruhiko, Oda Yoshinao, Ozaki Toshifumi, Tanaka Kazuhiro

机构信息

Department of Orthopaedic Surgery, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.

Department of Orthopaedic Surgery, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.

出版信息

Jpn J Clin Oncol. 2025 Mar 5;55(3):297-303. doi: 10.1093/jjco/hyae160.

Abstract

The optimal timing of surgery and the number of courses of perioperative chemotherapy for high-risk soft tissue sarcoma patients are still controversial. Tumour growth during neoadjuvant chemotherapy led to limb amputation in some patients. This study aims to confirm the non-inferiority of surgery and three courses of adjuvant chemotherapy with adriamycin (30 mg/m2, days 1 and 2) plus ifosfamide (2 g/m2, days 1-5) compared with our standard treatment of three courses of neoadjuvant chemotherapy and surgery followed by two courses of adjuvant chemotherapy with adriamycin plus ifosfamide for localized high-risk soft tissue sarcoma patients. This is a multi-center, two-arm, open-label, randomized phase III trial. The primary aim is to confirm the non-inferiority in overall survival (margin: hazard ratio of 1.61). This is the first randomized controlled trial to compare neoadjuvant chemotherapy and immediate surgery for soft tissue sarcoma. This trial was initiated on 16 November 2022 and registered with the Japan Clinical Trials Registry (jRCTs031220446).

摘要

高危软组织肉瘤患者手术的最佳时机以及围手术期化疗的疗程数仍存在争议。新辅助化疗期间肿瘤生长导致部分患者肢体截肢。本研究旨在证实,对于局限性高危软组织肉瘤患者,与我们的标准治疗(三个疗程新辅助化疗后手术,然后进行两个疗程阿霉素加异环磷酰胺辅助化疗)相比,手术加三个疗程阿霉素(30mg/m²,第1天和第2天)加异环磷酰胺(2g/m²,第1 - 5天)辅助化疗的非劣效性。这是一项多中心、双臂、开放标签的随机III期试验。主要目的是证实总生存的非劣效性(界值:风险比为1.61)。这是第一项比较软组织肉瘤新辅助化疗和即刻手术的随机对照试验。该试验于2022年11月16日启动,并在日本临床试验注册中心(jRCTs031220446)注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0b6/11882499/be77036ce55d/hyae160f1.jpg

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