Efficacy and safety of first-line carboplatin-versus cisplatin-based chemotherapy for non-small cell lung cancer: A meta-analysis.


Journal

Lung cancer (Amsterdam, Netherlands)
ISSN: 1872-8332
Titre abrégé: Lung Cancer
Pays: Ireland
ID NLM: 8800805

Informations de publication

Date de publication:
09 2019
Historique:
received: 14 06 2019
accepted: 12 07 2019
entrez: 27 8 2019
pubmed: 27 8 2019
medline: 14 7 2020
Statut: ppublish

Résumé

Platinum-based chemotherapy is the mainstay of first-line (1L) therapy for advanced non-small cell cancer (NSCLC). The objective of this study was to evaluate the relative efficacy, safety, and health-related quality of life (HRQoL) of carboplatin- versus cisplatin-based chemotherapy in 1L NSCLC. A meta-analysis by the Cochrane group (2013) was updated. Systematic searches of CENTRAL, Medline, Embase, Latin American and Caribbean Health Sciences database, clinicaltrials.gov and conference proceedings were conducted to include randomized controlled trials (RCTs) published between 2013-January 2018 which compared carboplatin and cisplatin combined with: gemcitabine, vinorelbine, docetaxel, paclitaxel, irinotecan, or pemetrexed. Endpoints included overall survival (OS), one-year OS, objective response rate (ORR), grade 3/4 drug-related toxicities, and HRQoL. Twelve RCTs (2,048 patients) were identified from 4,139 records for inclusion in the meta-analysis. There were no significant differences in OS (hazards ratio [HR]: 1.08, 95% confidence interval [CI]: 0.96, 1.21) and one-year OS (relative risk [RR]: 0.97, CI: 0.89, 1.07) between carboplatin- and cisplatin-based chemotherapy. A small effect on ORR favouring cisplatin was detected (RR = 0.88; CI: 0.78, 0.99). Differences in drug-related toxicities were observed between carboplatin- and cisplatin-based chemotherapy for thrombocytopenia, anaemia, neurotoxicity, and the risk of nausea/vomiting. Three RCTs comparing HRQoL between carboplatin- and cisplatin-based chemotherapy found no significant differences. This updated evidence base corroborates findings of previous meta-analyses showing no difference in OS between carboplatin- and cisplatin-based chemotherapy, despite a slight benefit in ORR for cisplatin. Toxicity profiles should be considered alongside patients' comorbidities in the choice of therapy.

Identifiants

pubmed: 31446995
pii: S0169-5002(19)30550-1
doi: 10.1016/j.lungcan.2019.07.010
pii:
doi:

Substances chimiques

Carboplatin BG3F62OND5
Cisplatin Q20Q21Q62J

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

196-204

Informations de copyright

Copyright © 2019 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Frank Griesinger (F)

Pius-Hospital, University Medicine Oldenburg, Department of Hematology and Oncology, University Department Internal Medicine-Oncology, 26121, Oldenburg, Germany. Electronic address: Griesinger@Pius-Hospital.de.

Ellen E Korol (EE)

ICON plc., Vancouver, V6B 1P1, Canada.

Sheena Kayaniyil (S)

ICON plc., Vancouver, V6B 1P1, Canada. Electronic address: sheena.kayaniyil@iconplc.com.

Nebibe Varol (N)

Bristol-Myers Squibb Pharmaceuticals Ltd., Uxbridge, UB8 1DH, UK. Electronic address: nebibe.varol@bms.com.

Timo Ebner (T)

Bristol-Myers Squibb GmbH&Co. KGaA, 80636, München, Germany. Electronic address: timo.ebner@bms.com.

Sarah M Goring (SM)

ICON plc., Vancouver, V6B 1P1, Canada.

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