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A Guide to Selecting Flexible Survival Models to Inform Economic Evaluations of Cancer Immunotherapies.
Palmer, Stephen; Borget, Isabelle; Friede, Tim; Husereau, Don; Karnon, Jonathan; Kearns, Ben; Medin, Emma; Peterse, Elisabeth F P; Klijn, Sven L; Verburg-Baltussen, Elisabeth J M; Fenwick, Elisabeth; Borrill, John.
Afiliação
  • Palmer S; Centre for Health Economics, University of York, York, England, UK.
  • Borget I; Biostatistics and Epidemiology office, Gustave Roussy, Paris-Saclay University, Villejuif, France; Oncostat, Paris-Saclay University U1018, Inserm, Paris-Saclay University, "Ligue Contre le Cancer" labeled team, Villejuif, France.
  • Friede T; Department of Medical Statistics, University Medical Center Göttingen, Göttingen, Germany.
  • Husereau D; School of Epidemiology and Public Health, University of Ottawa, Ottawa, ON, Canada.
  • Karnon J; Flinders Health and Medical Research Institute, Flinders University, Adelaide, SA, Australia.
  • Kearns B; School of Health and Related Research, University of Sheffield, Sheffield, England, UK.
  • Medin E; Parexel International, Stockholm, Sweden; Department of Learning, Infomatics, Management and Ethics, Karolinska Institutet, Stockholm, Sweden.
  • Peterse EFP; Modeling & Meta-analysis, OPEN Health, Rotterdam, The Netherlands.
  • Klijn SL; Worldwide Health Economics and Outcomes Research - Economic and Predictive Modeling, Bristol Myers Squibb, Utrecht, The Netherlands.
  • Verburg-Baltussen EJM; Modeling & Meta-analysis, OPEN Health, Rotterdam, The Netherlands.
  • Fenwick E; Modeling & Meta-analysis, OPEN Health, Oxford, England, UK.
  • Borrill J; Worldwide Health Economics and Outcomes Research, Bristol Myers Squibb, Uxbridge, Greater London, England, UK. Electronic address: john.borrill@bms.com.
Value Health ; 26(2): 185-192, 2023 02.
Article em En | MEDLINE | ID: mdl-35970706
ABSTRACT

OBJECTIVES:

Parametric models are routinely used to estimate the benefit of cancer drugs beyond trial follow-up. The advent of immune checkpoint inhibitors has challenged this paradigm, and emerging evidence suggests that more flexible survival models, which can better capture the shapes of complex hazard functions, might be needed for these interventions. Nevertheless, there is a need for an algorithm to help analysts decide whether flexible models are required and, if so, which should be chosen for testing. This position article has been produced to bridge this gap.

METHODS:

A virtual advisory board comprising 7 international experts with in-depth knowledge of survival analysis and health technology assessment was held in summer 2021. The experts discussed 24 questions across 6 topics the current survival model selection procedure, data maturity, heterogeneity of treatment effect, cure and mortality, external evidence, and additions to existing guidelines. Their responses culminated in an algorithm to inform selection of flexible survival models.

RESULTS:

The algorithm consists of 8 steps and 4 questions. Key elements include the systematic identification of relevant external data, using clinical expert input at multiple points in the selection process, considering the future and the observed hazard functions, assessing the potential for long-term survivorship, and presenting results from all plausible models.

CONCLUSIONS:

This algorithm provides a systematic, evidence-based approach to justify the selection of survival extrapolation models for cancer immunotherapies. If followed, it should reduce the risk of selecting inappropriate models, partially addressing a key area of uncertainty in the economic evaluation of these agents.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias / Antineoplásicos Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias / Antineoplásicos Idioma: En Ano de publicação: 2023 Tipo de documento: Article