Published November 2019 | Version v1
Journal article

Impact of pathological stage and histological subtype on clinical outcome of adjuvant chemotherapy of paclitaxel plus carboplatin versus oral uracil–tegafur for non-small cell lung cancer: subanalysis of SLCG0401 trial

  • 1. Okayama University, Department of General Thoracic Surgery and Breast and Endocrinological Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences (Japan)
  • 2. Kurashiki Central Hospital, Department of Thoracic Surgery (Japan)
  • 3. Tottori University Hospital, Division of General Thoracic Surgery (Japan)
  • 4. Kawasaki Medical School, Department of General Thoracic Surgery (Japan)
  • 5. Shikoku Cancer Center, Department of Thoracic Surgery (Japan)
  • 6. Tokai Central Hospital (Japan)
  • 7. Kagawa Prefectural Central Hospital, Department of Surgery (Japan)
  • 8. Okayama University Hospital, Center for Innovative Clinical Medicine (Japan)
  • 9. Kyoto University, Department of Biomedical Statistics and Bioinformatics (Japan)
  • 10. Kyoto University, Department of Thoracic Surgery (Japan)

Description

Background

Pathological stage (pStage) and histological subtype are strong determinants of the treatment strategy for non-small cell lung cancer (NSCLC). Setouchi Lung Cancer study Group (SLCG) recently reported the results of a multicenter trial (SLCG0401) indicating that paclitaxel plus carboplatin (CBDCA/PTX) as adjuvant chemotherapy does not yield better survival than uracil–tegafur (UFT) in NSCLC patients with pStage IB–IIIA disease, while stratified analyses considering the pStage and histological subtype have not been performed.

Methods

We reanalyzed the overall survival (OS) and relapse-free survival (RFS) in 402 patients who had been randomly assigned to receive CBDCA/PTX or UFT by multivariate analysis with adjustments for the pStage and histological subtype.

Results

There were no significant differences in the OS or RFS between the two treatment settings either in the entire cohort (n = 402) and in some of subsets: pStage IB (n = 228), pStage II (n = 117), adenocarcinoma (AD, n = 265), and squamous cell carcinoma (SQ, n = 101). In pStage IIIA patients (n = 57), CBDCA/PTX yielded superior RFS to UFT [hazard ratio (HR) 0.44; P = 0.016]. Among the patients with non-AD and non-SQ histology (n = 36), UFT yielded both superior OS and RFS to CBDCA/PTX (HRs 0.16 and 0.23; P = 0.046 and 0.011, respectively).

Conclusions

There are subsets of patients in which one or the other between UFT and CBDCA/PTX is significantly more effective. Selection of adjuvant therapy for NSCLC patients needs to be made taking into consideration the pStage and histological subtype.

Additional details

Identifiers

Publishing Information

Journal Title
International Journal of Clinical Oncology
Journal Volume
24
Journal Issue
11
Journal Page Range
p. 1367-1376
ISSN
1341-9625

INIS

Country of Publication
Japan
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
54122032
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
CARCINOMAS; CHEMOTHERAPY; HISTOLOGY; LUNGS; MULTIVARIATE ANALYSIS; PATIENTS; URACILS
Descriptors DEC
AZINES; BODY; DISEASES; HETEROCYCLIC COMPOUNDS; HYDROXY COMPOUNDS; MATHEMATICS; MEDICINE; NEOPLASMS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANS; PYRIMIDINES; RESPIRATORY SYSTEM; STATISTICS; THERAPY

Optional Information

Copyright
Copyright (c) 2019 Japan Society of Clinical Oncology