A Review of Overall Survival Extrapolations of Immune-Checkpoint Inhibitors Used in Health Technology Assessments by the French Health Authorities.

Cost-effectiveness analysis Extrapolation Immune-checkpoint inhibitors Modeling Overall survival

Journal

International journal of technology assessment in health care
ISSN: 1471-6348
Titre abrégé: Int J Technol Assess Health Care
Pays: England
ID NLM: 8508113

Informations de publication

Date de publication:
25 Mar 2022
Historique:
entrez: 25 3 2022
pubmed: 26 3 2022
medline: 29 3 2022
Statut: epublish

Résumé

Extrapolation is often required to inform cost-effectiveness (CE) evaluations of immune-checkpoint inhibitors (ICIs) since survival data from pivotal clinical trials are seldom complete. The objectives of this study were to evaluate the accuracy of estimates of long-term overall survival (OS) predicted in French CE assessment reports of ICIs, and to identify models presenting the best fit to the observed long-term survival data. A systematic review of French assessment reports of ICIs in the metastatic setting since inception until May 2020 was performed. A targeted literature review was conducted to collect associated extended follow-up of randomized controlled trials (RCTs) used in the CE assessment reports. Difference between projected and observed OS was calculated. A range of standard parametric and spline-based models were applied to the extended follow-up data from the RCT to determine the best-fitting survival models. Of the 121 CE assessment reports published, 11 reports met the inclusion criteria. OS was underestimated in 73 percent of the CE assessment reports. The mean relative difference between each source was -13 percent (median: -15 percent; IQR: -0.4 to 26 percent). Models providing the best fit were those that could reflect nonmonotonic hazards. Based on the available data at the time of submission, longer-term survival of ICIs was not fully captured by the extrapolation models used in CE assessments. Standard and flexible parametric models which can capture nonmonotonic hazard functions provided the best fit to the extended follow-up data. However, these models may still have performed poorly if fitted to survival data available at the time of submission to the French National Authority for Health.

Identifiants

pubmed: 35331347
doi: 10.1017/S0266462322000125
pii: S0266462322000125
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e28

Subventions

Organisme : Bristol Myers Squibb France

Commentaires et corrections

Type : ErratumIn

Auteurs

Valentine Grumberg (V)

Market access department, Bristol Myers Squibb France, Rueil-Malmaison, France.

Stéphane Roze (S)

Vyoo Agency, Lyon, France.

Julie Chevalier (J)

Vyoo Agency, Lyon, France.

John Borrill (J)

WW HEOR, Bristol Myers Squibb, Uxbridge, United Kingdom.

Anne-Françoise Gaudin (AF)

Market access department, Bristol Myers Squibb France, Rueil-Malmaison, France.

Sébastien Branchoux (S)

Market access department, Bristol Myers Squibb France, Rueil-Malmaison, France.

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Classifications MeSH