Value assessment of oncology drugs using a weighted criterion-based approach.

anticancer therapy multicriteria decision analysis value assessment value assessment framework

Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
01 04 2020
Historique:
received: 31 05 2019
revised: 09 10 2019
accepted: 24 10 2019
pubmed: 21 12 2019
medline: 6 11 2020
entrez: 21 12 2019
Statut: ppublish

Résumé

Globally, the rising cost of anticancer therapy has motivated efforts to quantify the overall value of new cancer treatments. Multicriteria decision analysis offers a novel approach to incorporate multiple criteria and perspectives into value assessment. The authors recruited a diverse, multistakeholder group who identified and weighted key criteria to establish the drug assessment framework (DAF). Construct validity assessed the degree to which DAF scores were associated with past pan-Canadian Oncology Drug Review (pCODR) funding recommendations and European Society for Medical Oncology Magnitude of Clinical Benefit Scale (ESMO-MCBS; version 1.1) scores. The final DAF included 10 criteria: overall survival, progression-free survival, response rate, quality of life, toxicity, unmet need, equity, feasibility, disease severity, and caregiver well-being. The first 5 clinical benefit criteria represent approximately 64% of the total weight. DAF scores ranged from 0 to 300, reflecting both the expected impact of the drug and the quality of supporting evidence. When the DAF was applied to the last 60 drugs (with reviewers blinded) reviewed by pCODR (2015-2018), those drugs with positive pCODR funding recommendations were found to have higher DAF scores compared with drugs not recommended (103 vs 63; Student t test P = .0007). DAF clinical benefit criteria mildly correlated with ESMO-MCBS scores (correlation coefficient, 0.33; 95% CI, 0.009-0.59). Sensitivity analyses that varied the criteria scores did not change the results. Using a structured and explicit approach, a criterion-based valuation framework was designed to provide a transparent and consistent method with which to value and prioritize cancer drugs to facilitate the delivery of affordable cancer care.

Sections du résumé

BACKGROUND
Globally, the rising cost of anticancer therapy has motivated efforts to quantify the overall value of new cancer treatments. Multicriteria decision analysis offers a novel approach to incorporate multiple criteria and perspectives into value assessment.
METHODS
The authors recruited a diverse, multistakeholder group who identified and weighted key criteria to establish the drug assessment framework (DAF). Construct validity assessed the degree to which DAF scores were associated with past pan-Canadian Oncology Drug Review (pCODR) funding recommendations and European Society for Medical Oncology Magnitude of Clinical Benefit Scale (ESMO-MCBS; version 1.1) scores.
RESULTS
The final DAF included 10 criteria: overall survival, progression-free survival, response rate, quality of life, toxicity, unmet need, equity, feasibility, disease severity, and caregiver well-being. The first 5 clinical benefit criteria represent approximately 64% of the total weight. DAF scores ranged from 0 to 300, reflecting both the expected impact of the drug and the quality of supporting evidence. When the DAF was applied to the last 60 drugs (with reviewers blinded) reviewed by pCODR (2015-2018), those drugs with positive pCODR funding recommendations were found to have higher DAF scores compared with drugs not recommended (103 vs 63; Student t test P = .0007). DAF clinical benefit criteria mildly correlated with ESMO-MCBS scores (correlation coefficient, 0.33; 95% CI, 0.009-0.59). Sensitivity analyses that varied the criteria scores did not change the results.
CONCLUSIONS
Using a structured and explicit approach, a criterion-based valuation framework was designed to provide a transparent and consistent method with which to value and prioritize cancer drugs to facilitate the delivery of affordable cancer care.

Identifiants

pubmed: 31860138
doi: 10.1002/cncr.32639
doi:

Substances chimiques

Antineoplastic Agents 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1530-1540

Subventions

Organisme : CIHR
Pays : Canada

Informations de copyright

© 2019 American Cancer Society.

Références

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Auteurs

Doreen A Ezeife (DA)

Department of Oncology, Tom Baker Cancer Centre, Calgary, Alberta, Canada.

Francois Dionne (F)

Prioritize Consulting Ltd, Vancouver, British Columbia, Canada.

Aline Fusco Fares (AF)

Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.

Ellen Laura Rose Cusano (ELR)

Department of Oncology, Tom Baker Cancer Centre, Calgary, Alberta, Canada.

Rouhi Fazelzad (R)

Department of Medical Oncology and Hematology, Library and Information Services, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.

Wenzie Ng (W)

Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.

Don Husereau (D)

School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.

Farzad Ali (F)

Pfizer Inc, New York, New York.

Christina Sit (C)

Lung Cancer Canada, Toronto, Ontario, Canada.

Barry Stein (B)

Colorectal Cancer Canada, Montreal, Quebec, Canada.

Jennifer H Law (JH)

Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.

Lisa Le (L)

Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.

Peter Michael Ellis (PM)

Juravinski Cancer Centre, Hamilton, Ontario, Canada.

Scott Berry (S)

Cancer Centre of Southeastern Ontario, Kingston, Ontario, Canada.

Stuart Peacock (S)

British Columbia Cancer Agency, Vancouver, British Columbia, Canada.

Craig Mitton (C)

The University of British Columbia, Vancouver, British Columbia, Canada.

Craig C Earle (CC)

Sunnybrook Odette Cancer Centre, Toronto, Ontario, Canada.

Kelvin K W Chan (KKW)

Sunnybrook Odette Cancer Centre, Toronto, Ontario, Canada.

Natasha B Leighl (NB)

Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.

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