Cost-effectiveness of ribociclib for premenopausal or perimenopausal women with HR+/HER2- advanced breast cancer: a Brazilian public health care system perspective.

CDK inhibitors breast cancer cost-effectiveness overall survival ribociclib

Journal

Therapeutic advances in medical oncology
ISSN: 1758-8340
Titre abrégé: Ther Adv Med Oncol
Pays: England
ID NLM: 101510808

Informations de publication

Date de publication:
2022
Historique:
received: 07 01 2022
accepted: 28 04 2022
entrez: 7 11 2022
pubmed: 8 11 2022
medline: 8 11 2022
Statut: epublish

Résumé

The MONALEESA-7 trial compared ribociclib plus endocrine therapy (ET) with placebo as first-line treatment of advanced luminal/HER2-negative breast cancer (ABC) in premenopausal and perimenopausal women (age <50 years) and showed significant benefits to progression-free survival and overall survival. This study aimed to compare the cost-effectiveness of ribociclib + ET We calculated the incremental cost-effectiveness ratio (ICER) using a Markov model with progression-free survival, post-progression survival, and death states. We expressed ICER as incremental costs per progression-free life-year (PFLY) and quality-adjusted life-year (QALY) gained in a 10-year time horizon. We used parametric survival distributions fit to MONALEESA-7 data to generate survival distributions for progression-free and post-progression survival. The largest British preference study in breast cancer served as the basis to estimate health-state utilities. We estimated direct costs (ABC treatment, follow-up, monitoring, and adverse events) using Brazilian-specific values from public sources. An expert consensus panel determined the resource patterns required. We applied annual discounts of 5% to costs and QALYs. Ribociclib + ET resulted in an incremental gain of 1.03 PFLYs and 0.80 QALYs at a cost of $37,319.31. The ICER of ribociclib + ET Ribociclib increased PFLYs and QALYs in patients with HR+/HER2- ABC when added to ET. Because Brazil does not have a formally defined cost-effectiveness threshold, other domains need to be considered for incorporation decisions, such as disease burden and humanistic impact on this young, economically active population. These findings may be useful in discussions for incorporation of ribociclib into the Brazilian public health system.

Identifiants

pubmed: 36339925
doi: 10.1177/17588359221100865
pii: 10.1177_17588359221100865
pmc: PMC9634995
doi:

Types de publication

Journal Article

Langues

eng

Pagination

17588359221100865

Informations de copyright

© The Author(s), 2022.

Déclaration de conflit d'intérêts

The authors declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: A.M.B. and M.S. are employers of Novartis Biociências S.A. The other authors received fees for the composite of the consensus panel.

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Auteurs

Daniela Dornelles Rosa (DD)

Oncology, Grupo Brasileiro de Estudos do Câncer de Mama (GBECAM), São Paulo, BrazilOncology, Hospital Moinhos de Vento (HMV), Porto Alegre, Brazil.

Carlos Alberto da Silva Magliano (CADS)

Oncology, Asas Avaliações Econômicas em Saúde Ltda, Rio de Janeiro, Brazil.

Sergio D Simon (SD)

Oncology, Grupo Brasileiro de Estudos do Câncer de Mama (GBECAM), São Paulo, Brazil.
Oncology, Grupo Oncoclinicas, São Paulo, BrazilOncology, Hospital Israelita Albert Einstein, São Paulo, Brazil.

Gilberto Amorim (G)

Oncology, Grupo Brasileiro de Estudos do Câncer de Mama (GBECAM), São Paulo, Brazil.
Oncology, Instituto D'Or de Pesquisa e Ensino (IDOR), Rio de Janeiro, Brazil.

Tomás Reinert (T)

Oncology, Grupo Brasileiro de Estudos do Câncer de Mama (GBECAM), São Paulo, Brazil.
Oncology, Centro de Pesquisa da Serra Gaúcha (CEPESG), Caxias do Sul, Brazil.

Luciana Landeiro (L)

Oncology, Grupo Brasileiro de Estudos do Câncer de Mama (GBECAM), São Paulo, Brazil.
Oncology, Grupo Oncoclínicas Bahia, Salvador, Brazil.

Débora de Melo Gagliato (DM)

Oncology, Grupo Brasileiro de Estudos do Câncer de Mama (GBECAM), São Paulo, Brazil.
Oncology, Beneficência Portuguesa, São Paulo, Brazil.

Pedro Exman (P)

Oncology, Grupo Brasileiro de Estudos do Câncer de Mama (GBECAM), São Paulo, Brazil.
Oncology, Hospital Alemão Oswaldo Cruz, São Paulo, Brazil; Oncology, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil.

Daniel Argolo (D)

Oncology, Grupo Brasileiro de Estudos do Câncer de Mama (GBECAM), São Paulo, Brazil.
Oncology, Clion/Grupo CAM, Salvador, Brazil.

Gisah Guilgen (G)

Oncology, Grupo Brasileiro de Estudos do Câncer de Mama (GBECAM), São Paulo, Brazil.
Oncology, Instituto do Câncer e Transplante de Curitiba, Curitiba, Brazil.

Max Mano (M)

Oncology, Grupo Brasileiro de Estudos do Câncer de Mama (GBECAM), São Paulo, Brazil.
Oncology, Grupo Oncoclínicas, São Paulo, BrazilOncology, Centro Paulista de Oncologia, São Paulo, Brazil.

Laura Testa (L)

Oncology, Grupo Brasileiro de Estudos do Câncer de Mama (GBECAM), São Paulo, Brazil.
Oncology, Instituto D'Or de Pesquisa e Ensino (IDOR), São Paulo, Brazil.
Oncology, Instituto do Câncer do Estado de São Paulo, São Paulo, Brazil.

Pedro Liedke (P)

Oncology, Grupo Brasileiro de Estudos do Câncer de Mama (GBECAM), São Paulo, Brazil.
Oncology, Hospital das Clínicas de Porto Alegre (HCPA), Porto Alegre, BrazilOncology, Grupo Oncoclínicas Porto Alegre, Porto Alegre, Brazil.

Romualdo Barroso (R)

Oncology, Grupo Brasileiro de Estudos do Câncer de Mama (GBECAM), São Paulo, Brazil.
Oncology, Hospital Sírio Libanês, Brasília, Brazil.

Mariana Sasse (M)

Oncology, Novartis Biociências S.A., São Paulo, Brazil.

Anna Maria Buehler (AM)

Oncology, Novartis Biociências S.A., Professor Vicente Rao Avenue, 90, 04636-000 São Paulo, SP, Brazil.

Classifications MeSH