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Real-World Impact of Adjuvant Anti-HER2 Treatment on Characteristics and Outcomes of Women With HER2-Positive Metastatic Breast Cancer in the ESME Program

BACKGROUND: Although adjuvant cancer treatments increase cure rates, they may induce clonal selection and tumor resistance. Information still lacks as whether (neo)adjuvant anti-HER2 treatments impact the patterns of recurrence and outcomes of HER2-positive (HER2+) metastatic breast cancer (MBC). We...

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Autores principales: Le Du, Fanny, Carton, Matthieu, Bachelot, Thomas, Saghatchian, Mahasti, Pistilli, Barbara, Brain, Etienne, Loirat, Delphine, Vanlemmens, Laurence, Vermeulin, Thomas, Emile, George, Gonçalves, Anthony, Ung, Mony, Robert, Marie, Jaffre, Anne, Desmoulins, Isabelle, Jouannaud, Christelle, Uwer, Lionel, Marc Ferrero, Jean, Mouret-Reynier, Marie-Ange, Jacot, William, Chevrot, Michaël, Delaloge, Suzette, Diéras, Véronique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10546827/
https://www.ncbi.nlm.nih.gov/pubmed/37589218
http://dx.doi.org/10.1093/oncolo/oyad137
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author Le Du, Fanny
Carton, Matthieu
Bachelot, Thomas
Saghatchian, Mahasti
Pistilli, Barbara
Brain, Etienne
Loirat, Delphine
Vanlemmens, Laurence
Vermeulin, Thomas
Emile, George
Gonçalves, Anthony
Ung, Mony
Robert, Marie
Jaffre, Anne
Desmoulins, Isabelle
Jouannaud, Christelle
Uwer, Lionel
Marc Ferrero, Jean
Mouret-Reynier, Marie-Ange
Jacot, William
Chevrot, Michaël
Delaloge, Suzette
Diéras, Véronique
author_facet Le Du, Fanny
Carton, Matthieu
Bachelot, Thomas
Saghatchian, Mahasti
Pistilli, Barbara
Brain, Etienne
Loirat, Delphine
Vanlemmens, Laurence
Vermeulin, Thomas
Emile, George
Gonçalves, Anthony
Ung, Mony
Robert, Marie
Jaffre, Anne
Desmoulins, Isabelle
Jouannaud, Christelle
Uwer, Lionel
Marc Ferrero, Jean
Mouret-Reynier, Marie-Ange
Jacot, William
Chevrot, Michaël
Delaloge, Suzette
Diéras, Véronique
author_sort Le Du, Fanny
collection PubMed
description BACKGROUND: Although adjuvant cancer treatments increase cure rates, they may induce clonal selection and tumor resistance. Information still lacks as whether (neo)adjuvant anti-HER2 treatments impact the patterns of recurrence and outcomes of HER2-positive (HER2+) metastatic breast cancer (MBC). We aimed to assess this in the large multicenter ESME real-world database. PATIENTS AND METHODS: We examined the characteristics and outcomes (overall survival (OS) and progression-free survival under first-line treatment (PFS1)) of HER2+ patients with MBC from the French ESME program with recurrent disease, as a function of the previous receipt of adjuvant trastuzumab. Multivariable analyses used Cox models adjusted for baseline demographic, prognostic factors, adjuvant treatment received, and disease-free interval. RESULTS: Two thousand one hundred and forty-three patients who entered the ESME cohort between 2008 and 2017 had a recurrent HER2+ MBC. Among them, 56% had received (neo)adjuvant trastuzumab and 2.5% another anti-HER2 in this setting. Patients pre-exposed to trastuzumab were younger, had a lower disease-free interval, more HR-negative disease and more metastatic sites. While the crude median OS appeared inferior in patients exposed to adjuvant trastuzumab, as compared to those who did not (37.2 (95%CI 34.4-40.3) versus 53.5 months (95% CI: 47.6-60.1)), this difference disappeared in the multivariable model (HR = 1.05, 95%CI 0.91-1.22). The same figures were observed for PFS1. CONCLUSIONS: Among patients with relapsed HER2+ MBC, the receipt of adjuvant trastuzumab did not independently predict for worse outcomes when adjusted to other prognostic factors.
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spelling pubmed-105468272023-10-04 Real-World Impact of Adjuvant Anti-HER2 Treatment on Characteristics and Outcomes of Women With HER2-Positive Metastatic Breast Cancer in the ESME Program Le Du, Fanny Carton, Matthieu Bachelot, Thomas Saghatchian, Mahasti Pistilli, Barbara Brain, Etienne Loirat, Delphine Vanlemmens, Laurence Vermeulin, Thomas Emile, George Gonçalves, Anthony Ung, Mony Robert, Marie Jaffre, Anne Desmoulins, Isabelle Jouannaud, Christelle Uwer, Lionel Marc Ferrero, Jean Mouret-Reynier, Marie-Ange Jacot, William Chevrot, Michaël Delaloge, Suzette Diéras, Véronique Oncologist Breast Cancer BACKGROUND: Although adjuvant cancer treatments increase cure rates, they may induce clonal selection and tumor resistance. Information still lacks as whether (neo)adjuvant anti-HER2 treatments impact the patterns of recurrence and outcomes of HER2-positive (HER2+) metastatic breast cancer (MBC). We aimed to assess this in the large multicenter ESME real-world database. PATIENTS AND METHODS: We examined the characteristics and outcomes (overall survival (OS) and progression-free survival under first-line treatment (PFS1)) of HER2+ patients with MBC from the French ESME program with recurrent disease, as a function of the previous receipt of adjuvant trastuzumab. Multivariable analyses used Cox models adjusted for baseline demographic, prognostic factors, adjuvant treatment received, and disease-free interval. RESULTS: Two thousand one hundred and forty-three patients who entered the ESME cohort between 2008 and 2017 had a recurrent HER2+ MBC. Among them, 56% had received (neo)adjuvant trastuzumab and 2.5% another anti-HER2 in this setting. Patients pre-exposed to trastuzumab were younger, had a lower disease-free interval, more HR-negative disease and more metastatic sites. While the crude median OS appeared inferior in patients exposed to adjuvant trastuzumab, as compared to those who did not (37.2 (95%CI 34.4-40.3) versus 53.5 months (95% CI: 47.6-60.1)), this difference disappeared in the multivariable model (HR = 1.05, 95%CI 0.91-1.22). The same figures were observed for PFS1. CONCLUSIONS: Among patients with relapsed HER2+ MBC, the receipt of adjuvant trastuzumab did not independently predict for worse outcomes when adjusted to other prognostic factors. Oxford University Press 2023-08-17 /pmc/articles/PMC10546827/ /pubmed/37589218 http://dx.doi.org/10.1093/oncolo/oyad137 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Breast Cancer
Le Du, Fanny
Carton, Matthieu
Bachelot, Thomas
Saghatchian, Mahasti
Pistilli, Barbara
Brain, Etienne
Loirat, Delphine
Vanlemmens, Laurence
Vermeulin, Thomas
Emile, George
Gonçalves, Anthony
Ung, Mony
Robert, Marie
Jaffre, Anne
Desmoulins, Isabelle
Jouannaud, Christelle
Uwer, Lionel
Marc Ferrero, Jean
Mouret-Reynier, Marie-Ange
Jacot, William
Chevrot, Michaël
Delaloge, Suzette
Diéras, Véronique
Real-World Impact of Adjuvant Anti-HER2 Treatment on Characteristics and Outcomes of Women With HER2-Positive Metastatic Breast Cancer in the ESME Program
title Real-World Impact of Adjuvant Anti-HER2 Treatment on Characteristics and Outcomes of Women With HER2-Positive Metastatic Breast Cancer in the ESME Program
title_full Real-World Impact of Adjuvant Anti-HER2 Treatment on Characteristics and Outcomes of Women With HER2-Positive Metastatic Breast Cancer in the ESME Program
title_fullStr Real-World Impact of Adjuvant Anti-HER2 Treatment on Characteristics and Outcomes of Women With HER2-Positive Metastatic Breast Cancer in the ESME Program
title_full_unstemmed Real-World Impact of Adjuvant Anti-HER2 Treatment on Characteristics and Outcomes of Women With HER2-Positive Metastatic Breast Cancer in the ESME Program
title_short Real-World Impact of Adjuvant Anti-HER2 Treatment on Characteristics and Outcomes of Women With HER2-Positive Metastatic Breast Cancer in the ESME Program
title_sort real-world impact of adjuvant anti-her2 treatment on characteristics and outcomes of women with her2-positive metastatic breast cancer in the esme program
topic Breast Cancer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10546827/
https://www.ncbi.nlm.nih.gov/pubmed/37589218
http://dx.doi.org/10.1093/oncolo/oyad137
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