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Multinational Randomized Phase III Trial With or Without Consolidation Chemotherapy Using Docetaxel and Cisplatin After Concurrent Chemoradiation in Inoperable Stage III Non-Small-Cell Lung Cancer: KCSG-LU05-04

Authors
Ahn, Jin SeokAhn, Yong ChanKim, Joo-HangLee, Chang GeolCho, Eun KyungLee, Kyu ChanChen, MingKim, Dong-WanKim, Hoon-KyoMin, Young JooKang, Jin-HyoungChoi, Jin-HyuckKim, Sang-WeZhu, GuangyingWu, Yi-LongKim, Sung RokLee, Kyung HeeSong, Hong SukChoi, Yoon-LaSun, Jong-MuJung, Sin-HoAhn, Myung-JuPark, Keunchil
Issue Date
20-Aug-2015
Publisher
AMER SOC CLINICAL ONCOLOGY
Citation
JOURNAL OF CLINICAL ONCOLOGY, v.33, no.24, pp.2660 - U124
Journal Title
JOURNAL OF CLINICAL ONCOLOGY
Volume
33
Number
24
Start Page
2660
End Page
U124
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/10255
DOI
10.1200/JCO.2014.60.0130
ISSN
0732-183X
Abstract
Purpose To determine the efficacy of consolidation chemotherapy (CC) with docetaxel and cisplatin (DP) after concurrent chemoradiotherapy (CCRT) with the same agents in locally advanced non-small-cell lung cancer (LA-NSCLC). Patient and Methods Patients were randomly assigned to either CCRT alone (observation arm) or CCRT followed by CC (consolidation arm). CCRT with docetaxel (20 mg/m(2)) and cisplatin (20 mg/m(2)) was administered every week for 6 weeks with a total dose of 66 Gy of thoracic radiotherapy in 33 fractions. In the consolidation arm, patients were further treated with three cycles of DP (35 mg/m(2) each on days 1 and 8, every 3 weeks). The primary end point was 40% improvement in progression-free survival (PFS) compared with observation. Results From October 2005 to April 2011, 437 patients were randomly assigned. Seventeen patients did not start CCRT as a result of consent withdrawal or ineligibility reasons after random assignment, leaving 420 patients for this analysis (n = 211 for observation; n = 209 for consolidation). Patient characteristics were similar in both arms. In the consolidation arm, 143 patients (68%) received CC, of whom 88 (62%) completed three planned cycles. The median PFS was 8.1 months in the observation arm and 9.1 months in the consolidation arm (hazard ratio, 0.91; 95% CI, 0.73 to 1.12; P = .36). Median overall survival times were 20.6 and 21.8 months in the observation and consolidation arms, respectively (HR, 0.91; 95% CI, 0.72 to 1.25; P = .44). Conclusion CC with DP after CCRT with weekly DP in LA-NSCLC failed to further prolong PFS. CCRT alone should remain the standard of care. (C) 2015 by American Society of Clinical Oncology
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