Association of Chemoradiotherapy With Outcomes Among Patients With Stage I to II vs Stage III Small Cell Lung Cancer: Secondary Analysis of a Randomized Clinical Trial.
Aged
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Chemoradiotherapy
/ adverse effects
Cisplatin
/ administration & dosage
Disease Progression
Dose Fractionation, Radiation
Etoposide
/ administration & dosage
Female
Humans
Lung Neoplasms
/ mortality
Male
Middle Aged
Neoplasm Staging
Progression-Free Survival
Prospective Studies
Radiotherapy, Conformal
/ adverse effects
Small Cell Lung Carcinoma
/ mortality
Time Factors
Journal
JAMA oncology
ISSN: 2374-2445
Titre abrégé: JAMA Oncol
Pays: United States
ID NLM: 101652861
Informations de publication
Date de publication:
01 03 2019
01 03 2019
Historique:
pubmed:
7
12
2018
medline:
20
12
2019
entrez:
7
12
2018
Statut:
ppublish
Résumé
There is limited evidence to guide stage I to II small cell lung cancer (SCLC) treatment. To examine the characteristics and outcomes among patients with stage I to II SCLC treated with modern chemoradiotherapy. In this post hoc secondary analysis of the Concurrent Once-Daily vs Twice-Daily Radiotherapy Trial (CONVERT), a multicenter phase 3 trial conducted in patients with limited-stage SCLC from April 7, 2008, to November 29, 2013, patients with TNM stage I to II SCLC were compared with those with stage III disease. Data analysis was performed from November 1, 2017, to February 28, 2018. In CONVERT, patients were randomized to receive twice-daily (45 Gy in 30 fractions) or once-daily (66 Gy in 33 fractions) chemoradiotherapy. Prophylactic cranial irradiation (PCI) was offered, if indicated. The primary trial end point was overall survival (OS). TNM staging information was collected prospectively; this was an unplanned analysis because stratification was not performed according to TNM stage. A total of 509 (277 [54.4%] men; mean [SD] age, 61.5 [8.3] years) of 543 patients (93.7%) with TNM staging information were eligible for this subgroup analysis, and 86 of the 509 (16.9%) had TNM stage I to II disease. The median gross tumor volume was smaller in patients with stage I to II disease (38.4 cm3; range, 2.2-593.0 cm3) compared with patients with stage III disease (93 cm3; range, 0.5-513.4 cm3) (P < .001). No other significant differences were found in baseline and treatment characteristics and chemoradiotherapy adherence between the 2 groups or the number of patients with stage I to II disease (78 [90.7%]) and stage III disease (346 [81.8%]) who received PCI (P = .10). Patients with stage I to II disease achieved longer OS (median, 50 months [95% CI, 38 to not reached months] vs 25 months [95% CI, 21-29 months]; hazard ratio, 0.60 [95% CI, 0.44-0.83]; P = .001) compared with patients with stage III disease. In patients with stage I to II disease, no significant survival difference was found between the trial arms (median, 39 months in the once-daily arm vs 72 months in the twice-daily arm; P = .38). Apart from lower incidence of acute esophagitis in patients with stage I to II disease compared with patients with stage III disease (grade ≥3, 9 [11.3%] vs 82 [21.1%]; P < .001), the incidences of acute and late toxic effects were not significantly different. Patients with stage I to II SCLC in CONVERT achieved long-term survival with acceptable toxic effects after chemoradiotherapy and PCI. This study suggests that patients with stage I to II small cell lung cancer treated with modern chemoradiotherapy have better outcomes compared with patients with stage III disease, providing information that practitioners can potentially give their patients to aid clinical decisions. ClinicalTrials.gov identifier: NCT00433563.
Identifiants
pubmed: 30520977
pii: 2717236
doi: 10.1001/jamaoncol.2018.5335
pmc: PMC6439849
doi:
Substances chimiques
Etoposide
6PLQ3CP4P3
Cisplatin
Q20Q21Q62J
Banques de données
ClinicalTrials.gov
['NCT00433563']
Types de publication
Clinical Trial, Phase III
Comparative Study
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e185335Subventions
Organisme : Cancer Research UK
ID : 8154
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C17052/A8154
Pays : United Kingdom
Commentaires et corrections
Type : CommentIn
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