Cost-effectiveness analysis of adjuvant atezolizumab in stage II-IIIA non-small cell lung cancer expressing ≥50% PD-L1: A United Kingdom health care perspective.


Journal

Lung cancer (Amsterdam, Netherlands)
ISSN: 1872-8332
Titre abrégé: Lung Cancer
Pays: Ireland
ID NLM: 8800805

Informations de publication

Date de publication:
05 2023
Historique:
received: 14 12 2022
revised: 28 02 2023
accepted: 13 03 2023
medline: 3 5 2023
pubmed: 23 3 2023
entrez: 22 3 2023
Statut: ppublish

Résumé

Atezolizumab monotherapy has marketing authorisation by the Medicines and Healthcare products Regulatory Agency as adjuvant treatment following complete resection for adults with stage II-IIIA non-small cell lung cancer (NSCLC) whose tumours have PD-L1 expression on ≥ 50% of tumour cells and whose disease has not progressed following adjuvant platinum-based chemotherapy. This study evaluated the cost-effectiveness of atezolizumab vs best supportive care (BSC) in the licensed patient population from a UK perspective. Patient characteristics and clinical inputs were derived from the global, randomised, open-label, phaseIII IMpower010 trial. A Markov model with the following health states was developed: disease-free survival (DFS), locoregional recurrence, first-line metastatic recurrence, second-line metastatic recurrence, and death (all partitioned based on receipt of treatment, excluding death). The base case model used a lifetime time horizon (40 years) and 3.5% discounting annually after the first year. DFS from IMpower010 was analysed with parametric survival models to extrapolate outcomes for time points beyond trial follow-up. The models were adjusted to avoid overestimating results for patients with recurrences in the longer term. Grade ≥ 3 treatment-related adverse events with incidences ≥ 2% were included. Health state utility values were derived from the literature and past NICE appraisals. Sensitivity and scenario analyses assessed uncertainty around assumptions and parameter estimates. In the base case analysis, atezolizumab therapy resulted in an expected gain of 1.87 quality-adjusted life-years (QALYs) corresponding to an incremental cost-effectiveness ratio of £20,392/QALY for atezolizumab vs BSC, demonstrating cost-effectiveness. Results were most influenced by discount effects and utility in the on-treatment DFS state. Scenario analyses were consistent with the base case results. Atezolizumab after adjuvant chemotherapy is cost-effective for adults with NSCLC in the UK.

Identifiants

pubmed: 36947997
pii: S0169-5002(23)00094-6
doi: 10.1016/j.lungcan.2023.03.007
pii:
doi:

Substances chimiques

atezolizumab 52CMI0WC3Y
B7-H1 Antigen 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

107171

Informations 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 that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Chui-Ying Yip (CY)

Roche Products Ltd, Welwyn Garden City, United Kingdom. Electronic address: chui-ying.yip@roche.com.

Alastair Greystoke (A)

Northern Centre for Cancer Care, Newcastle upon Tyne, UK, United Kingdom.

Seye Abogunrin (S)

F. Hoffmann-La Roche Ltd, Basel, Switzerland.

Rossella Belleli (R)

F. Hoffmann-La Roche Ltd, Basel, Switzerland.

Danilo Di Maio (D)

F. Hoffmann-La Roche Ltd, Basel, Switzerland.

Peter Rouse (P)

Roche Products Ltd, Welwyn Garden City, United Kingdom.

Nick Jovanoski (N)

F. Hoffmann-La Roche Ltd, Basel, Switzerland.

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Classifications MeSH