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Contextualizing pertuzumab approval in the treatment of HER2-positive breast cancer patients.
Cortés, Javier; Ciruelos, Eva; Pérez-García, José; Albanell, Joan; García-Estévez, Laura; Ruiz-Borrego, Manuel; Espinosa, Ruth; Gallegos, Isabel; González, Santiago; Álvarez, Isabel; Llombart, Antonio.
Afiliación
  • Cortés J; IOB Institute of Oncology, Quirónsalud Group, Madrid & Barcelona, Spain; Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain. Electronic address: jacortes@vhio.net.
  • Ciruelos E; Hospital Universitario 12 de Octubre, Madrid, Spain; HM Centro Integral Oncológico Clara Campal (CIOCC), Madrid, Spain; SOLTI Breast Cancer Research Cooperative Group, Spain.
  • Pérez-García J; IOB Institute of Oncology, Quirónsalud Group, Madrid & Barcelona, Spain; Medica Scientia Innovation Research (MedSIR), Barcelona, Spain.
  • Albanell J; Hospital de Mar, Barcelona, Spain.
  • García-Estévez L; MD Anderson Cancer Center, Madrid, Spain.
  • Ruiz-Borrego M; Hospital Virgen del Rocío, Sevilla, Spain.
  • Espinosa R; Hospital General La Mancha Centro, Alcázar de San Juan, Ciudad Real, Spain.
  • Gallegos I; Hospital General de Segovia, Spain.
  • González S; Hospital Universitario San Pedro de Alcántara, Cáceres, Spain.
  • Álvarez I; Hospital Universitario Donostia, San Sebastián, Spain.
  • Llombart A; Hospital Arnau Vilanova, Valencia, and Universidad Católica de Valencia, Spain.
Cancer Treat Rev ; 83: 101944, 2020 Feb.
Article en En | MEDLINE | ID: mdl-31830538
The use of adjuvant pertuzumab in HER2-positive early-stage breast cancer has recently been approved by the EMA on the basis of data from the APHINITY trial. Accordingly, we have produced this opinion article with the aim of putting the study data in perspective against other add-on therapeutic strategies, to clarify methodological or statistical doubts about the study, and to define the population of high-risk patients with hormone receptor-negative breast cancer that we agree, in general, should be treated. With this approval, physicians must be well prepared to place the APHINITY study data in context. It is now up to each country to ratify the EMA-approved indications and to agree on reimbursement, and doctors must optimize their use based on knowledge and discussion with patients.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Aprobación de Drogas / Receptor ErbB-2 / Anticuerpos Monoclonales Humanizados / Antineoplásicos Inmunológicos Límite: Female / Humans Idioma: En Revista: Cancer Treat Rev Año: 2020 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Aprobación de Drogas / Receptor ErbB-2 / Anticuerpos Monoclonales Humanizados / Antineoplásicos Inmunológicos Límite: Female / Humans Idioma: En Revista: Cancer Treat Rev Año: 2020 Tipo del documento: Article Pais de publicación: Países Bajos