PS5-11-01: Cost-effectiveness analysis of next-generation sequencing (ngs) panel including brca1 and brca2 genes for women diagnosed with non-metastatic breast cancer in brazil

Abstract Background: Pathogenic BRCA1/2 mutations in women diagnosed with non-metastatic breast cancer (MBC) correlate with worse survival outcomes and elevated risk of contralateral breast cancer. Detecting pathogenic BRCA1/2 mutations via next-generation sequencing panels (NGS) provides clinical benefits by optimizing treatment strategies. Objective: This study estimates the cost-effectiveness of using NGS with genetic counselling to detect pathogenic BRCA1/2 mutations in women diagnosed with non-MBC, compared to no genetic testing, from the perspective of Brazil's Public Health System. Methods: A hybrid economic model (decision tree plus Markov model) simulated costs and outcomes over a 10-year horizon of NGS with genetic counselling to identify pathogenic BRCA1/2 mutations in women diagnosed with non-MBC. The eligible population was estimated by using epidemiological methods using national data identified in the literature. Were estimated the incremental cost-effectiveness ratio (ICER) per quality-adjusted life year (QALY) gained of adding NGS plus genetic counselling to identify pathogenic BRCA1/2 mutations in women diagnosed with non-MBC. Results: NGS for pathogenic BRCA1/2 mutations combined with genetic counselling showed an incremental benefit of 0.044 QALYs gained at an additional cost of US$ 590.29 compared to no genetic testing and genetic counselling, resulting in an ICER of US$ 13,526.89 per QALY gained. Conclusion: NGS for pathogenic BRCA1/2 mutations combined with genetic counselling was cost-effective from the Brazilian public health system perspective, with an ICER value below the Brazilian oncological willingness-to-pay threshold of US$21,500/QALY (R$120,000.00/QALY). Citation Format: H. L. Couto, R. M. Rahal, A. T. Hassan, F. Zanghelini, L. P. Gargano, T. C. Oliveira, B. A. Coelho, M. C. Wender, A. L. Silva, E. C. Pessoa, A. Mattar, C. A. Padua, G. F. Cunha Júnior, A. M. Santos, L. L. Dominguez, D. R. Siqueira, M. S. Castilho, M. Antonini, J. S. Oliveira, B. A. Pires, D. d. Pires, S. d. Ferreira, T. P. Moraes, L. B. Oliveira, P. C. Soares, R. G. Saliba, A. C. Mendonça, J. C. Cisneros, F. M. Reis, G. Novita, V. M. Oliveira, F. M. Bagnoli, G. Tosello, D. d. Buttros, B. P. Carvalho, W. J. Almeida Junior, M. d. Ramos, D. Balabram, É. M. Carvalho, BreastMit Collaborative Research Group. Cost-effectiveness analysis of next-generation sequencing (ngs) panel including brca1 and brca2 genes for women diagnosed with non-metastatic breast cancer in brazil [abstract]. In: Proceedings of the San Antonio Breast Cancer Symposium 2025; 2025 Dec 9-12; San Antonio, TX. Philadelphia (PA): AACR; Clin Cancer Res 2026;32(4 Suppl):Abstract nr PS5-11-01.

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Journal
Clinical Cancer Research
Published
2026-02-17
DOI
https://doi.org/10.1158/1557-3265.sabcs25-ps5-11-01
Primary Topic
BRCA gene mutations in cancer
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article
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article

PS5-11-01: Cost-effectiveness analysis of next-generation sequencing (ngs) panel including brca1 and brca2 genes for women diagnosed with non-metastatic breast cancer in brazil

Marcelo Antonini, Giuliano Tosello, André Mattar, Débora Balabram et al.
Clinical Cancer Research
BRCA gene mutations in cancer
article

PS5-11-01: Cost-effectiveness analysis of next-generation sequencing (ngs) panel including brca1 and brca2 genes for women diagnosed with non-metastatic breast cancer in brazil

Marcelo Antonini, Giuliano Tosello, André Mattar, Débora Balabram, Fernando Zanghelini, M. C. Wender, F. M. Reis, T. C. Oliveira, A. T. Hassan, T. P. Moraes, F. M. Bagnoli, D. d. Buttros, D. R. Siqueira, R. G. Saliba, B. A. Coelho, C. A. Padua, B. P. Carvalho, J. S. Oliveira, M. S. Castilho, J. C. Cisneros, W. J. Almeida Junior, G. F. Cunha Júnior, A. C. Mendonça, A. M. Santos, R. Macedo Sousa Rahal, V. M. Oliveira, E. C. Pessoa, L. L. Dominguez, H. L. Couto, G. Novita, A. L. Silva, L. B. Oliveira, L. P. Gargano, P. C. Soares, É. M. Carvalho, S. d. Ferreira, M. d. Ramos, D. d. Pires, B. A. Pires
article en

Abstract

Abstract Background: Pathogenic BRCA1/2 mutations in women diagnosed with non-metastatic breast cancer (MBC) correlate with worse survival outcomes and elevated risk of contralateral breast cancer. Detecting pathogenic BRCA1/2 mutations via next-generation sequencing panels (NGS) provides clinical benefits by optimizing treatment strategies. Objective: This study estimates the cost-effectiveness of using NGS with genetic counselling to detect pathogenic BRCA1/2 mutations in women diagnosed with non-MBC, compared to no genetic testing, from the perspective of Brazil's Public Health System. Methods: A hybrid economic model (decision tree plus Markov model) simulated costs and outcomes over a 10-year horizon of NGS with genetic counselling to identify pathogenic BRCA1/2 mutations in women diagnosed with non-MBC. The eligible population was estimated by using epidemiological methods using national data identified in the literature. Were estimated the incremental cost-effectiveness ratio (ICER) per quality-adjusted life year (QALY) gained of adding NGS plus genetic counselling to identify pathogenic BRCA1/2 mutations in women diagnosed with non-MBC. Results: NGS for pathogenic BRCA1/2 mutations combined with genetic counselling showed an incremental benefit of 0.044 QALYs gained at an additional cost of US$ 590.29 compared to no genetic testing and genetic counselling, resulting in an ICER of US$ 13,526.89 per QALY gained. Conclusion: NGS for pathogenic BRCA1/2 mutations combined with genetic counselling was cost-effective from the Brazilian public health system perspective, with an ICER value below the Brazilian oncological willingness-to-pay threshold of US$21,500/QALY (R$120,000.00/QALY). Citation Format: H. L. Couto, R. M. Rahal, A. T. Hassan, F. Zanghelini, L. P. Gargano, T. C. Oliveira, B. A. Coelho, M. C. Wender, A. L. Silva, E. C. Pessoa, A. Mattar, C. A. Padua, G. F. Cunha Júnior, A. M. Santos, L. L. Dominguez, D. R. Siqueira, M. S. Castilho, M. Antonini, J. S. Oliveira, B. A. Pires, D. d. Pires, S. d. Ferreira, T. P. Moraes, L. B. Oliveira, P. C. Soares, R. G. Saliba, A. C. Mendonça, J. C. Cisneros, F. M. Reis, G. Novita, V. M. Oliveira, F. M. Bagnoli, G. Tosello, D. d. Buttros, B. P. Carvalho, W. J. Almeida Junior, M. d. Ramos, D. Balabram, É. M. Carvalho, BreastMit Collaborative Research Group. Cost-effectiveness analysis of next-generation sequencing (ngs) panel including brca1 and brca2 genes for women diagnosed with non-metastatic breast cancer in brazil [abstract]. In: Proceedings of the San Antonio Breast Cancer Symposium 2025; 2025 Dec 9-12; San Antonio, TX. Philadelphia (PA): AACR; Clin Cancer Res 2026;32(4 Suppl):Abstract nr PS5-11-01.

Clinical Cancer ResearchVol. 32(4_Supplement)
Universidade Federal de Minas Gerais (BR), Universidade Federal do Rio Grande do Sul (BR), Breast Cancer Research Foundation (US), Universidade do Estado de Minas Gerais (BR), Universidade Federal de Pernambuco (BR), Brazilian Computer Society (BR), Centro Universitário de Belo Horizonte (BR), Universidade do Oeste Paulista (BR), Centro Universitário Claretiano (BR), Hospital do Servidor Público Municipal (BR), Faculdade de Ciências Médicas de Minas Gerais (BR), Faculdade de Ciências Médicas da Santa Casa de São Paulo (BR), Medecell (Brazil) (BR), Grupo Santa Casa de Belo Horizonte (BR), Hospital Regional de Presidente Prudente (BR), Sociedade Brasileira de Anestesiologia (BR), Tokushima Red Cross Hospital (JP), Southeast Radiation Oncology Group (US), Hospital São Paulo (BR), Universidade Estadual de Montes Claros (BR), Fundação Oswaldo Cruz (BR), Universidade Federal de Goiás (BR), Universidade Estadual Paulista (Unesp) (BR)
Good health and well-being
Openalex Percentile: Top 50%
BRCA gene mutations in cancer
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