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.


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
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

e185335

Subventions

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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Auteurs

Ahmed Salem (A)

Division of Cancer Sciences, University of Manchester, Manchester, United Kingdom.

Hitesh Mistry (H)

Division of Pharmacy, University of Manchester, Manchester, United Kingdom.

Matthew Hatton (M)

Weston Park Hospital, Sheffield, United Kingdom.

Imogen Locke (I)

Royal Marsden Hospital, Surrey, United Kingdom.

Isabelle Monnet (I)

Centre Hospitalier Intercommunal de Créteil, Créteil, France.

Fiona Blackhall (F)

Division of Cancer Sciences, University of Manchester, Manchester, United Kingdom.

Corinne Faivre-Finn (C)

Division of Cancer Sciences, University of Manchester, Manchester, United Kingdom.

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Classifications MeSH