The evolving landscape of immunotherapy in small-cell lung cancer: A focus on predictive biomarkers.
Antineoplastic Agents, Immunological
/ therapeutic use
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Biomarkers, Tumor
Clinical Trials as Topic
Combined Modality Therapy
Humans
Immunomodulation
/ drug effects
Immunotherapy
/ methods
Lung Neoplasms
/ immunology
Molecular Targeted Therapy
Small Cell Lung Carcinoma
/ immunology
Treatment Outcome
Atezolizumab
Checkpoint inhibitors
PD-L1
Pembrolizumab
SCLC
Tumor mutational burden
Journal
Cancer treatment reviews
ISSN: 1532-1967
Titre abrégé: Cancer Treat Rev
Pays: Netherlands
ID NLM: 7502030
Informations de publication
Date de publication:
Sep 2019
Sep 2019
Historique:
received:
16
02
2019
revised:
28
07
2019
accepted:
06
08
2019
pubmed:
7
9
2019
medline:
24
9
2019
entrez:
7
9
2019
Statut:
ppublish
Résumé
Small cell lung cancer (SCLC) was defined as a "recalcitrant cancer" because of its dismal prognosis and lack of outcome improvements in the last 30 years. Immunotherapy with checkpoint inhibitors revolutionized treatment in many cancer types and results from the IMpower133 study, a double-blind placebo-controlled phase III trial, showed overall survival benefit for atezolizumab when added to standard platinum-etoposide chemotherapy in first-line SCLC setting for the first time since years. Trials with other checkpoint inhibitors, e.g. pembrolizumab, durvalumab, nivolumab and ipilimumab, are ongoing in various settings, but, to date, there are no defined factors to identify patients who are more likely to benefit from such treatments. This review summarizes results of immunotherapy trials in SCLC for first-line, maintenance and further-line therapies for single-agents and combinations with checkpoint inhibitors. Predictive factors from these trials are reviewed in order to identify their clinical value, with particular emphasis on PD-L1 expression on both tumor cells and in stroma, especially in pembrolizumab-treated patients, and tumor mutational burden, for patients treated with the ipilimumab and nivolumab combination.
Identifiants
pubmed: 31491661
pii: S0305-7372(19)30094-5
doi: 10.1016/j.ctrv.2019.08.003
pii:
doi:
Substances chimiques
Antineoplastic Agents, Immunological
0
Biomarkers, Tumor
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
101887Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.