Cost-effectiveness analysis of atezolizumab as adjuvant treatment of patients with stage II-IIIA non-small cell lung cancer, PD-L1+≥50% of tumor cells in France: A modeling study.
Humans
Carcinoma, Non-Small-Cell Lung
/ pathology
B7-H1 Antigen
/ genetics
Lung Neoplasms
/ drug therapy
Cost-Effectiveness Analysis
Cost-Benefit Analysis
Neoplasm Recurrence, Local
/ drug therapy
ErbB Receptors
Receptor Protein-Tyrosine Kinases
/ therapeutic use
Quality-Adjusted Life Years
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Adjuvant therapy
Atezolizumab
Cost-effectiveness model
Markov
Non-small cell lung cancer
Journal
Lung cancer (Amsterdam, Netherlands)
ISSN: 1872-8332
Titre abrégé: Lung Cancer
Pays: Ireland
ID NLM: 8800805
Informations de publication
Date de publication:
10 2023
10 2023
Historique:
received:
20
04
2023
revised:
18
07
2023
accepted:
24
07
2023
medline:
19
9
2023
pubmed:
11
8
2023
entrez:
10
8
2023
Statut:
ppublish
Résumé
The objective of this study was to assess the cost-effectiveness of atezolizumab versus best supportive care (BSC) as adjuvant treatment following resection and platinum-based chemotherapy for patients with stage II-IIIA non-small cell lung cancer (NSCLC) whose tumours have a programmed death-ligand 1 (PD-L1) expression ≥ 50% of tumour cells and excluding those with ALK/EGFR mutations, from a French collective perspective. A five state Markov model over a 20-year time horizon was considered, including disease-free survival (DFS Atezolizumab was associated with a QALY gain of 1.662, mainly driven by additional time spent in the DFS state, and a life-year gain of 2.112 years. The incremental cost-effectiveness ratio (ICER) for atezolizumab versus BSC was €21,348/QALY gained. The sensitivity analyses highlighted that uncertainty within the model had limited impact on results. Changing the DFS survival curves to other plausible distributions produced ICERs below €20,000/QALY. Introducing an increasing proportion of cured patients (91.5%) from year two to year five reduced the ICER to €13,083/QALY, while including a loss of efficacy at year two in the atezolizumab treatment arm increased the ICER to €33,755/QALY. Atezolizumab as adjuvant treatment in stage II-IIIA NSCLC resected patients with PDL1 ≥ 50% and without ALK/EGFR mutations has a lower ICER than other oncology drugs in France and a similar ICER to other adjuvant treatment in oncology.
Identifiants
pubmed: 37562344
pii: S0169-5002(23)00854-1
doi: 10.1016/j.lungcan.2023.107316
pii:
doi:
Substances chimiques
atezolizumab
52CMI0WC3Y
CD274 protein, human
0
B7-H1 Antigen
0
ErbB Receptors
EC 2.7.10.1
Receptor Protein-Tyrosine Kinases
EC 2.7.10.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
107316Informations de copyright
Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: [Ingrid Plessala, Hélène Cawston and Justine Cortes are employees of Amaris Consulting, which received professional fees from Roche SAS France for the study, and which has also received fees for projects outside the present study. Roula Ajjouri and Katell Le Lay are employees of Roche SAS France. Roche SAS France provided professional fees to Amaris Consulting for the project, including preparation of the manuscript. Pierre-Jean Souquet and, Christos Chouaid received fees for this project and provided clinical advice to Roche SAS France, as clinical experts. They also participated to advisory boards, to the manuscript development and its review].