A multi-institutional randomized phase III study comparing weekly carboplatin plus nab-paclitaxel and daily low-dose carboplatin as regimens for concurrent chemoradiotherapy in elderly patients with unresectable locally advanced non-small cell lung cancer: Japan Clinical Oncology Group Study JCOG1914

被引:8
|
作者
Shimoyama, Ryo [1 ]
Omori, Shota [2 ]
Nomura, Shogo [1 ]
Kenmotsu, Hirotsugu [2 ]
Takahashi, Toshiaki [2 ]
Harada, Hideyuki [3 ]
Ishikura, Satoshi [4 ]
Mizutani, Tomonori [5 ]
Ando, Masahiko [6 ]
Kataoka, Tomoko [1 ]
Fukuda, Haruhiko [1 ]
Ohe, Yuichiro [7 ]
机构
[1] Natl Canc Ctr, JCOG Data Ctr, Operat Off, Tokyo, Japan
[2] Shizuoka Canc Ctr, Div Thorac Oncol, Shizuoka, Japan
[3] Shizuoka Canc Ctr, Radiat & Proton Therapy Ctr, Shizuoka, Japan
[4] Nagoya City Univ, Dept Radiol, Grad Sch Med Sci, Nagoya, Aichi, Japan
[5] Kyorin Univ, Dept Med Oncol, Fac Med, Tokyo, Japan
[6] Nagoya Univ Hosp, Dept Adv Med, Nagoya, Aichi, Japan
[7] Natl Canc Ctr, Dept Thorac Oncol, Tokyo, Japan
关键词
randomized controlled trial; carboplatin; nab-paclitaxel; radiotherapy; non-small cell lung cancer; ALBUMIN-BOUND PACLITAXEL; QUALITY-OF-LIFE; FUNCTIONAL ASSESSMENT; TRIAL; THERAPY; VALIDITY;
D O I
10.1093/jjco/hyab025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Daily low-dose carboplatin plus concurrent thoracic radiotherapy is the standard treatment for elderly patients with unresectable clinical stage (c-Stage) III non-small cell lung cancer (NSCLC) in Japan. However, a phase I study by Omori et al. suggests that weekly carboplatin and nab-paclitaxel plus concurrent thoracic radiotherapy have comparable efficacy outcomes with more manageable adverse events. In December 2020, we initiated a randomized controlled trial in Japan to confirm whether the weekly carboplatin plus nab-paclitaxel regimen is noninferior to the daily low-dose carboplatin regimen for concurrent chemoradiotherapy in elderly patients with unresectable c-Stage III NSCLC. We plan to enroll 166 patients from 50 institutions in 3.5 years. The primary endpoint is overall survival. The secondary endpoints are progression-free survival, response rate, proportion of patients starting maintenance durvalumab therapy, adverse events, site of progression, Functional Assessment of Cancer Therapy-Trial Outcome Index deterioration and Instrumental Activities of Daily Living deterioration.
引用
收藏
页码:836 / 841
页数:6
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