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Oncofertility counselling in premenopausal women with HER2-positive breast cancer

A complete oncofertility counselling should be offered to all premenopausal patients before the administration of anticancer treatments. This important discussion is a crucial step for allowing them to take fully informed decisions about the proposed therapy and its potential long-term consequences...

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Autores principales: Lambertini, Matteo, Demeestere, Isabelle, Viglietti, Giulia, de Azambuja, Evandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398182/
https://www.ncbi.nlm.nih.gov/pubmed/30847021
http://dx.doi.org/10.18632/oncotarget.26565
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author Lambertini, Matteo
Demeestere, Isabelle
Viglietti, Giulia
de Azambuja, Evandro
author_facet Lambertini, Matteo
Demeestere, Isabelle
Viglietti, Giulia
de Azambuja, Evandro
author_sort Lambertini, Matteo
collection PubMed
description A complete oncofertility counselling should be offered to all premenopausal patients before the administration of anticancer treatments. This important discussion is a crucial step for allowing them to take fully informed decisions about the proposed therapy and its potential long-term consequences as well as on their need and interest of accessing the available strategies for ovarian function and/or fertility preservation. In premenopausal women with HER2-positive early breast cancer, limited evidence exists to counsel them about the potential added gonadotoxicity of targeted agents beyond the damage already caused by chemotherapy. In addition, the prognostic role of treatment-induced amenorrhea in this setting was unknown. In our exploratory analysis within the ALTTO (BIG 2-06) trial, we have recently described the rates of treatment-induced amenorrhea after chemotherapy plus trastuzumab and/or lapatinib and the prognostic value of developing this side effect according to the hormone receptor status of their tumours. We observed similar rates of treatment-induced amenorrhea in the four anti-HER2 treatment arms. The lack of an increased rate of treatment-induced amenorrhea in the dual anti-HER2 blockade arm suggests the possible gonadal safety of these agents. In addition, women with HER2-positive/hormone receptor-positive tumours showed significantly better survival outcomes if they developed treatment-induced amenorrhea, while no difference was observed for those with HER2-positive/hormone receptor-negative disease. Future research efforts are needed to address the gonadotoxicity of the new available targeted agents as well as to elucidate which is the best adjuvant endocrine therapy in premenopausal women with HER2-positive/hormone receptor-positive disease.
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spelling pubmed-63981822019-03-07 Oncofertility counselling in premenopausal women with HER2-positive breast cancer Lambertini, Matteo Demeestere, Isabelle Viglietti, Giulia de Azambuja, Evandro Oncotarget Research Perspective A complete oncofertility counselling should be offered to all premenopausal patients before the administration of anticancer treatments. This important discussion is a crucial step for allowing them to take fully informed decisions about the proposed therapy and its potential long-term consequences as well as on their need and interest of accessing the available strategies for ovarian function and/or fertility preservation. In premenopausal women with HER2-positive early breast cancer, limited evidence exists to counsel them about the potential added gonadotoxicity of targeted agents beyond the damage already caused by chemotherapy. In addition, the prognostic role of treatment-induced amenorrhea in this setting was unknown. In our exploratory analysis within the ALTTO (BIG 2-06) trial, we have recently described the rates of treatment-induced amenorrhea after chemotherapy plus trastuzumab and/or lapatinib and the prognostic value of developing this side effect according to the hormone receptor status of their tumours. We observed similar rates of treatment-induced amenorrhea in the four anti-HER2 treatment arms. The lack of an increased rate of treatment-induced amenorrhea in the dual anti-HER2 blockade arm suggests the possible gonadal safety of these agents. In addition, women with HER2-positive/hormone receptor-positive tumours showed significantly better survival outcomes if they developed treatment-induced amenorrhea, while no difference was observed for those with HER2-positive/hormone receptor-negative disease. Future research efforts are needed to address the gonadotoxicity of the new available targeted agents as well as to elucidate which is the best adjuvant endocrine therapy in premenopausal women with HER2-positive/hormone receptor-positive disease. Impact Journals LLC 2019-01-29 /pmc/articles/PMC6398182/ /pubmed/30847021 http://dx.doi.org/10.18632/oncotarget.26565 Text en Copyright: © 2019 Lambertini et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Perspective
Lambertini, Matteo
Demeestere, Isabelle
Viglietti, Giulia
de Azambuja, Evandro
Oncofertility counselling in premenopausal women with HER2-positive breast cancer
title Oncofertility counselling in premenopausal women with HER2-positive breast cancer
title_full Oncofertility counselling in premenopausal women with HER2-positive breast cancer
title_fullStr Oncofertility counselling in premenopausal women with HER2-positive breast cancer
title_full_unstemmed Oncofertility counselling in premenopausal women with HER2-positive breast cancer
title_short Oncofertility counselling in premenopausal women with HER2-positive breast cancer
title_sort oncofertility counselling in premenopausal women with her2-positive breast cancer
topic Research Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398182/
https://www.ncbi.nlm.nih.gov/pubmed/30847021
http://dx.doi.org/10.18632/oncotarget.26565
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