Addition of Immune Checkpoint Inhibitors to Chemotherapy vs Chemotherapy Alone as First-Line Treatment in Extensive-Stage Small-Cell Lung Carcinoma: A Systematic Review and Meta-Analysis.

Anti-PD-1/PD-L1 antibodies Chemotherapy Immunotherapy Meta-analysis Small cell lung carcinoma

Journal

Oncology and therapy
ISSN: 2366-1089
Titre abrégé: Oncol Ther
Pays: New Zealand
ID NLM: 101677510

Informations de publication

Date de publication:
Jun 2022
Historique:
received: 23 11 2021
accepted: 23 12 2021
pubmed: 16 1 2022
medline: 16 1 2022
entrez: 15 1 2022
Statut: ppublish

Résumé

The addition of immune checkpoint inhibitors (ICIs) to conventional chemotherapy (CT) as first-line treatment improves survival in extensive-stage small-cell lung cancer (ES-SCLC). The aim of this meta-analysis was to determine the relative efficacy of first-line ICIs compared with CT in patients with ES-SCLC. Two independent reviewers extracted relevant data according to PRISMA guidelines and assessed the risk of bias using the Cochrane Collaboration's risk-of-bias tool. Meta-analysis was conducted using random-effects models to calculate an average effect size for overall survival (OS), progression-free survival (PFS), and safety outcomes in the overall populations and clinically relevant subgroups. A literature search of PubMed and Embase was performed. Six randomized controlled clinical trials (IMpower133, CHECKMATE-451, CASPIAN, KEYNOTE-604, and phase II and III ipilimumab plus CT trials) with a total of 3757 patients were included. Compared with CT alone, ICIs plus CT showed a favourable effect on OS (hazard ratio [HR] 0.85; 95% confidence intervals [CI] 0.79-0.96) and PFS (HR 0.78; 95% CI 0.72-0.83) but a non-significant increase in the risk of experiencing any adverse event (relative risk, 1.05; 95% CI 0.99-1.11). The estimated HR for OS favoured ICI combinations in all planned subgroups according to age (< 65 years/≥ 65 years), sex (men/women), and ECOG performance status (0/1). Analysis by specific ICI revealed significant improvements in OS only for atezolizumab + CT (HR 1.36; 95% CI 1.09-1.69) and durvalumab + CT (HR 1.35; 95% CI 1.12-1.62) compared with CT alone. Combining anti-programmed cell death ligand 1 antibodies with platinum/etoposide is a superior therapeutic approach compared to CT alone for the first-line treatment of patients with ES-SCLC.

Identifiants

pubmed: 35032007
doi: 10.1007/s40487-021-00182-0
pii: 10.1007/s40487-021-00182-0
pmc: PMC9098752
doi:

Types de publication

Journal Article

Langues

eng

Pagination

167-184

Informations de copyright

© 2022. The Author(s).

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Auteurs

Edurne Arriola (E)

Medical Oncology Department, Hospital Universitari del Mar-CIBERONC, Passeig Marítim 25-29, 08003, Barcelona, Spain. earriola@parcdesalutmar.cat.

María González-Cao (M)

Medical Oncology Department (IOR), Hospital Dexeus, Barcelona, Spain.

Manuel Domine (M)

Medical Oncology Department, Fundación Jiménez Díaz, Madrid, Spain.

Javier De Castro (J)

Medical Oncology Department, Hospital Universitario La Paz, Madrid, Spain.

Manuel Cobo (M)

Inter-Center Medical Oncology Clinical Management Unit, Regional and Virgen de la Victoria University Hospitals, IBIMA, Málaga, Spain.

Reyes Bernabé (R)

Medical Oncology Department, Hospital Virgen del Rocío, Sevilla, Spain.

Alejandro Navarro (A)

Medical Oncology Department, Vall d'Hebron University Hospital & Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.

Ivana Sullivan (I)

Medical Oncology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

José Manuel Trigo (JM)

Medical Oncology Department, Hospital Virgen de la Victoria, Málaga, Spain.

Joaquín Mosquera (J)

Medical Oncology Department, Hospital Universitario A Coruña, A Coruña, Spain.

Leonardo Crama (L)

Medical Department Roche, Madrid, Spain.

Dolores Isla (D)

Medical Oncology Department, Hospital Universitario Lozano Blesa, Zaragoza, Spain.

Classifications MeSH