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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

  • Jin Seok Ahn
  • , Yong Chan Ahn
  • , Joo Hang Kim
  • , Chang Geol Lee
  • , Eun Kyung Cho
  • , Kyu Chan Lee
  • , Ming Chen
  • , Dong Wan Kim
  • , Hoon Kyo Kim
  • , Young Joo Min
  • , Jin Hyoung Kang
  • , Jin Hyuck Choi
  • , Sang We Kim
  • , Guangying Zhu
  • , Yi Long Wu
  • , Sung Rok Kim
  • , Kyung Hee Lee
  • , Hong Suk Song
  • , Yoon La Choi
  • , Jong Mu Sun
  • Sin Ho Jung, Myung Ju Ahn, Keunchil Park
  • Sungkyunkwan University
  • Yonsei University
  • Gachon University
  • Sun Yat-Sen University Cancer Center
  • Seoul National University
  • The Catholic University of Korea, St. Vincent's Hospital
  • University of Ulsan
  • Ajou University
  • Peking University
  • Guangdong Academy of Medical Sciences
  • Inje University
  • Yeungnam University
  • Keimyung University
  • Samsung Medical Center, Sungkyunkwan university

Research output: Contribution to journalArticlepeer-review

239 Scopus citations

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/m2) and cisplatin (20 mg/m2) 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/m2 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.

Original languageEnglish
Pages (from-to)2660-2666
Number of pages7
JournalJournal of Clinical Oncology
Volume33
Issue number24
DOIs
StatePublished - 20 Aug 2015

Bibliographical note

Publisher Copyright:
© 2015 by American Society of Clinical Oncology.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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