Immune checkpoint inhibitors versus second line chemotherapy for patients with lung cancer refractory to first line chemotherapy.
Adult
Aged
Aged, 80 and over
Antineoplastic Agents, Immunological
/ pharmacology
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Carcinoma, Non-Small-Cell Lung
/ diagnosis
Chemotherapy, Adjuvant
Drug Resistance, Neoplasm
/ drug effects
Female
France
Humans
Immune Checkpoint Inhibitors
/ pharmacology
Lung Neoplasms
/ diagnosis
Male
Middle Aged
Neoadjuvant Therapy
Prognosis
Retrospective Studies
Treatment Outcome
Chemotherapy
Immune checkpoint inhibitors
Non-small cell lung cancer
Prognosis
Journal
Respiratory medicine and research
ISSN: 2590-0412
Titre abrégé: Respir Med Res
Pays: France
ID NLM: 101746324
Informations de publication
Date de publication:
Nov 2020
Nov 2020
Historique:
received:
01
02
2020
revised:
17
05
2020
accepted:
20
08
2020
pubmed:
28
9
2020
medline:
28
9
2021
entrez:
27
9
2020
Statut:
ppublish
Résumé
Anti Programmed Death-ligand (PD1/PD-L1) directed immune-checkpoint-inhibitors (ICI) are widely used to treat patients with advanced non-small cell lung cancer (NSCLC) who progress after first line chemotherapy. The best strategy after early progression under first line has not been specifically studied. We conducted a multicenter, retrospective study including all consecutive NSCLC patients progressing within the first 3 months following introduction of first-line chemotherapy and being treated with second line ICI monotherapy or chemotherapy between March 2010 and November 2017. We analysed the clinicopathological data and outcome under second line chemotherapy vs. second line ICI: objective response rate (ORR), progression-free survival (PFS), overall survival (OS. We identified 176 patients with refractory disease, 99 who received subsequent immunotherapy and 77 undergoing chemotherapy. The 2 populations were comparable regarding the main prognostic criteria, median age was 60, main histology was adenocarcimoma (68.2%). PFS was not significantly different between both treatments 1.9 [1.8-2.1] versus 1.6 month [1.4-2.0] (P=0.125). Compared to chemotherapy, ICI treated patients had a superior OS (P=0.03) (Median [95% CI] OS 4.6 [2.8-6.7] versus 4.2 months [3.4-5.9] and a non-significant improvement in ORR (17.2% versus 7.9%, respectively, P=0.072). Poor performance status (ECOG PS≥2) and a higher number of metastatic sites (≥3) were associated with poorer prognosis. KRAS-mutated patients did not seem to benefit more from ICI than chemotherapy. ICI appears to be the preferred second-line treatment for patients who are refractory to first line chemotherapy.
Identifiants
pubmed: 32980653
pii: S2590-0412(20)30044-1
doi: 10.1016/j.resmer.2020.100788
pii:
doi:
Substances chimiques
Antineoplastic Agents, Immunological
0
Immune Checkpoint Inhibitors
0
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
100788Informations de copyright
Copyright © 2020. Published by Elsevier Masson SAS.