Choosing wisely first line immunotherapy in non-small cell lung cancer (NSCLC): what to add and what to leave out.
Antibodies, Monoclonal
/ therapeutic use
Antibodies, Monoclonal, Humanized
/ therapeutic use
Antineoplastic Agents
/ therapeutic use
B7-H1 Antigen
/ metabolism
Bevacizumab
/ therapeutic use
Carcinoma, Non-Small-Cell Lung
/ immunology
Humans
Immunologic Factors
/ metabolism
Immunotherapy
/ methods
Lung Neoplasms
/ immunology
Chemotherapy
First line treatment
Immunotherapy
NSCLC
Journal
Cancer treatment reviews
ISSN: 1532-1967
Titre abrégé: Cancer Treat Rev
Pays: Netherlands
ID NLM: 7502030
Informations de publication
Date de publication:
May 2019
May 2019
Historique:
received:
20
11
2018
revised:
23
03
2019
accepted:
27
03
2019
pubmed:
8
4
2019
medline:
27
4
2019
entrez:
8
4
2019
Statut:
ppublish
Résumé
Immunotherapy has dramatically changed the therapeutic scenario in treatment naïve advanced non-small cell lung cancer (NSCLC). While single agent pembrolizumab has become the standard therapy in patients with PD-L1 expression on tumor cells ≥ 50%, the combination of pembrolizumab or atezolizumab and platinum-based chemotherapy has emerged as an effective first line treatment regardless of PD-L1 expression both in squamous and non-squamous NSCLC without oncogenic drivers. Furthermore, double immune checkpoint inhibition has shown promising results in treatment naïve patients with high tumor mutational burden (TMB). Of note, the presence of both negative PD-L1 expression and low TMB may identify a subgroup of patients who has little benefit from immunotherapy combinations and for whom the best treatment option may still be platinum-based chemotherapy. To date, first-line single agent immune checkpoint blockade has demonstrated limited activity in EGFR mutated NSCLC and the combination of immunotherapy and targeted agents has raised safety concerns in both EGFR and ALK positive NSCLC patients. Finally, in EGFR mutated or ALK rearranged NSCLC, atezolizumab in combination with platinum-based chemotherapy and bevacizumab is emerging as a potential treatment option upon progression to first line tyrosine kinase inhibitors.
Identifiants
pubmed: 30954906
pii: S0305-7372(19)30052-0
doi: 10.1016/j.ctrv.2019.03.004
pii:
doi:
Substances chimiques
Antibodies, Monoclonal
0
Antibodies, Monoclonal, Humanized
0
Antineoplastic Agents
0
B7-H1 Antigen
0
Immunologic Factors
0
Bevacizumab
2S9ZZM9Q9V
atezolizumab
52CMI0WC3Y
pembrolizumab
DPT0O3T46P
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
39-51Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.