Final overall survival results of WJTOG3405, a randomized phase III trial comparing gefitinib versus cisplatin with docetaxel as the first-line treatment for patients with stage IIIB/IV or postoperative recurrent EGFR mutation-positive non-small-cell lung cancer.


Journal

Annals of oncology : official journal of the European Society for Medical Oncology
ISSN: 1569-8041
Titre abrégé: Ann Oncol
Pays: England
ID NLM: 9007735

Informations de publication

Date de publication:
01 12 2019
Historique:
pubmed: 26 9 2019
medline: 28 7 2020
entrez: 26 9 2019
Statut: ppublish

Résumé

Primary analysis of the phase III study WJTOG 3405 demonstrated superiority of progression-free survival (PFS) for gefitinib (G) in patients treated with the epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) gefitinib compared with cisplatin plus docetaxel (CD) as the first-line treatment of stage IIIB/IV or postoperative recurrent EGFR mutation-positive non-small-cell lung cancer. This report presents final overall survival (OS) data. Patients were randomized between G (250 mg/day orally) and cisplatin (80 mg/m2 intravenously) plus docetaxel (60 mg/m2 i.v.), administered every 21 days for three to six cycles. After the exclusion of 5 patients, 172 patients (86 in each group, modified intention-to-treat population) were included in the survival analysis. OS was re-evaluated using updated data (data cutoff, 30 September 2013; median follow-up time 59.1 months). The Kaplan-Meier method and the log-rank test were used for analysis, and hazard ratios (HRs) for death were calculated using the Cox proportional hazards model. OS events in the G group and CD group were 68 (79.1%) out of 86 and 59 (68.6%) out of 86, respectively. Median survival time for G and CD were 34.9 and 37.3 months, respectively, with an HR of 1.252 [95% confidence interval (CI): 0.883-1.775, P = 0.2070]. Multivariate analysis identified postoperative recurrence and stage IIIB/IV disease as independent prognostic factors, with an HR of 0.459 (95% CI: 0.312-0.673, P < 0.001). Median survival time (postoperative recurrence versus stage IIIB/IV disease) were 44.5 and 27.5 months in the G group and 45.5 and 32.8 months in the CD group, respectively. G did not show OS benefits over CD as the first-line treatment. OS of patients with postoperative recurrence was better than that of stage IIIB/IV disease, even though both groups had metastatic disease.This study was registered with UMIN (University Hospital Medical Information Network in Japan), number 000000539.

Sections du résumé

BACKGROUND
Primary analysis of the phase III study WJTOG 3405 demonstrated superiority of progression-free survival (PFS) for gefitinib (G) in patients treated with the epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) gefitinib compared with cisplatin plus docetaxel (CD) as the first-line treatment of stage IIIB/IV or postoperative recurrent EGFR mutation-positive non-small-cell lung cancer. This report presents final overall survival (OS) data.
PATIENTS AND METHODS
Patients were randomized between G (250 mg/day orally) and cisplatin (80 mg/m2 intravenously) plus docetaxel (60 mg/m2 i.v.), administered every 21 days for three to six cycles. After the exclusion of 5 patients, 172 patients (86 in each group, modified intention-to-treat population) were included in the survival analysis. OS was re-evaluated using updated data (data cutoff, 30 September 2013; median follow-up time 59.1 months). The Kaplan-Meier method and the log-rank test were used for analysis, and hazard ratios (HRs) for death were calculated using the Cox proportional hazards model.
RESULTS
OS events in the G group and CD group were 68 (79.1%) out of 86 and 59 (68.6%) out of 86, respectively. Median survival time for G and CD were 34.9 and 37.3 months, respectively, with an HR of 1.252 [95% confidence interval (CI): 0.883-1.775, P = 0.2070]. Multivariate analysis identified postoperative recurrence and stage IIIB/IV disease as independent prognostic factors, with an HR of 0.459 (95% CI: 0.312-0.673, P < 0.001). Median survival time (postoperative recurrence versus stage IIIB/IV disease) were 44.5 and 27.5 months in the G group and 45.5 and 32.8 months in the CD group, respectively.
CONCLUSION
G did not show OS benefits over CD as the first-line treatment. OS of patients with postoperative recurrence was better than that of stage IIIB/IV disease, even though both groups had metastatic disease.This study was registered with UMIN (University Hospital Medical Information Network in Japan), number 000000539.

Identifiants

pubmed: 31553438
pii: S0923-7534(20)32554-0
doi: 10.1093/annonc/mdz399
pii:
doi:

Substances chimiques

Protein Kinase Inhibitors 0
Docetaxel 15H5577CQD
EGFR protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1
Cisplatin Q20Q21Q62J
Gefitinib S65743JHBS

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1978-1984

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

H Yoshioka (H)

Department of Thoracic Oncology, Kansai Medical University Hospital, Hirakata.

M Shimokawa (M)

Department of Cancer Information Research, National Hospital Organization Kyushu Cancer Center, Fukuoka; Department of Biostatistics, Yamaguchi University Graduate School of Medicine, Ube.

T Seto (T)

Department of Thoracic Oncology, National Hospital Organization Kyushu Cancer Center, Fukuoka.

S Morita (S)

Department of Biomedical Statistics and Bioinformatics, Kyoto University Graduate School of Medicine, Kyoto.

Y Yatabe (Y)

Department of Pathology and Molecular Genetics, Aichi Cancer Center Hospital, Nagoya.

I Okamoto (I)

Research Institute for Diseases of the Chest, Graduate School of Medical Sciences, Kyusyu University, Fukuoka.

J Tsurutani (J)

Advanced Cancer Translational Research Institute, Showa University, Tokyo.

M Satouchi (M)

Department of Thoracic Oncology, Hyogo Cancer Center, Akashi.

T Hirashima (T)

Department of Thoracic Oncology, Osaka Habikino Medical Center, Habikino.

S Atagi (S)

Department of Thoracic Oncology, National Hospital Organization Kinki-chuo Chest Medical Center, Sakai.

K Shibata (K)

Department of Medical Oncology, Kouseiren Takaoka Hospital, Takaoka.

H Saito (H)

Department of Respiratory Medicine, Aichi Cancer Center Aichi Hospital, Okazaki.

S Toyooka (S)

Department of General Thoracic Surgery and Breast and Endocrinological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama.

N Yamamoto (N)

Internal Medicine III, Wakayama Medical University Hospital, Wakayama.

K Nakagawa (K)

Department of Medical Oncology, Kindai University Hospital, Osaka-Sayama.

T Mitsudomi (T)

Division of Thoracic Surgery, Department of Surgery, Kindai University Hospital, Osaka-Sayama, Japan. Electronic address: mitsudom@med.kindai.ac.jp.

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Classifications MeSH