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Front-Line Bevacizumab plus Chemotherapy with or without Maintenance Therapy for Metastatic Breast Cancer: An Observational Study by the Hellenic Oncology Research Group

Front-line bevacizumab (BEV) in combination with taxanes offers benefit in progression-free survival (PFS) in metastatic breast cancer (mBC). The medical records of mBC patients, treated with front-line BEV-based chemotherapy, were retrospectively reviewed in order to generate real life safety and e...

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Autores principales: Kokkali, Stefania, Saloustros, Emmanouil, Stefanou, Dimitra, Makrantonakis, Paris, Kentepozidis, Nikolaos, Boukovinas, Ioannis, Xenidis, Nikolaos, Katsaounis, Panagiotis, Ardavanis, Alexandros, Ziras, Nikolaos, Christopoulou, Athina, Rigas, George, Kalbakis, Kostas, Vardakis, Nikolaos, Emmanouilides, Christos, Athanasiadis, Ilias, Anagnostopoulos, Athanassios, Hatzidaki, Dora, Prinarakis, Efthimios, Simopoulou, Foteini, Kotsakis, Athanasios, Georgoulias, Vassilis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871254/
https://www.ncbi.nlm.nih.gov/pubmed/35200604
http://dx.doi.org/10.3390/curroncol29020105
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author Kokkali, Stefania
Saloustros, Emmanouil
Stefanou, Dimitra
Makrantonakis, Paris
Kentepozidis, Nikolaos
Boukovinas, Ioannis
Xenidis, Nikolaos
Katsaounis, Panagiotis
Ardavanis, Alexandros
Ziras, Nikolaos
Christopoulou, Athina
Rigas, George
Kalbakis, Kostas
Vardakis, Nikolaos
Emmanouilides, Christos
Athanasiadis, Ilias
Anagnostopoulos, Athanassios
Hatzidaki, Dora
Prinarakis, Efthimios
Simopoulou, Foteini
Kotsakis, Athanasios
Georgoulias, Vassilis
author_facet Kokkali, Stefania
Saloustros, Emmanouil
Stefanou, Dimitra
Makrantonakis, Paris
Kentepozidis, Nikolaos
Boukovinas, Ioannis
Xenidis, Nikolaos
Katsaounis, Panagiotis
Ardavanis, Alexandros
Ziras, Nikolaos
Christopoulou, Athina
Rigas, George
Kalbakis, Kostas
Vardakis, Nikolaos
Emmanouilides, Christos
Athanasiadis, Ilias
Anagnostopoulos, Athanassios
Hatzidaki, Dora
Prinarakis, Efthimios
Simopoulou, Foteini
Kotsakis, Athanasios
Georgoulias, Vassilis
author_sort Kokkali, Stefania
collection PubMed
description Front-line bevacizumab (BEV) in combination with taxanes offers benefit in progression-free survival (PFS) in metastatic breast cancer (mBC). The medical records of mBC patients, treated with front-line BEV-based chemotherapy, were retrospectively reviewed in order to generate real life safety and efficacy data. Patients with human epidermal growth factor receptor 2 (HER2)-negative mBC treated with front-line BEV in combination with chemotherapy were eligible. Maintenance therapy with BEV and/or hormonal agents was at the physicians’ discretion. Among the 387 included patients, the most common adverse events were anemia (61.9%, mainly grade 1), grade 3/4 neutropenia (16.5%), grade 1/2 fatigue (22.3%), and grade 1/2 neuropathy (19.6%). Dose reductions were required in 164 cycles (7.1%) and toxicity led to treatment discontinuation in 21 patients (5.4%). The median PFS and the median overall survival (OS) were 13.3 (95% CI: 11.7–14.8) and 32.3 months (95% CI: 27.7–36.9), respectively. Maintenance therapy, with hormonal agents (ET) and/or BEV, was associated with longer OS versus no maintenance therapy (47.2 versus 23.6 months; p < 0.001) in patients with hormone receptor (HR)-positive disease and BEV maintenance offered longer OS versus no maintenance in patients with HR-negative disease (52.8 versus 23.3; p = 0.023). These real-life data show that front-line BEV-based chemotherapy in HER2-negative mBC patients is an effective treatment with an acceptable toxicity profile. The potential benefit of maintenance treatment, especially ET, is important and warrants further research.
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spelling pubmed-88712542022-02-25 Front-Line Bevacizumab plus Chemotherapy with or without Maintenance Therapy for Metastatic Breast Cancer: An Observational Study by the Hellenic Oncology Research Group Kokkali, Stefania Saloustros, Emmanouil Stefanou, Dimitra Makrantonakis, Paris Kentepozidis, Nikolaos Boukovinas, Ioannis Xenidis, Nikolaos Katsaounis, Panagiotis Ardavanis, Alexandros Ziras, Nikolaos Christopoulou, Athina Rigas, George Kalbakis, Kostas Vardakis, Nikolaos Emmanouilides, Christos Athanasiadis, Ilias Anagnostopoulos, Athanassios Hatzidaki, Dora Prinarakis, Efthimios Simopoulou, Foteini Kotsakis, Athanasios Georgoulias, Vassilis Curr Oncol Article Front-line bevacizumab (BEV) in combination with taxanes offers benefit in progression-free survival (PFS) in metastatic breast cancer (mBC). The medical records of mBC patients, treated with front-line BEV-based chemotherapy, were retrospectively reviewed in order to generate real life safety and efficacy data. Patients with human epidermal growth factor receptor 2 (HER2)-negative mBC treated with front-line BEV in combination with chemotherapy were eligible. Maintenance therapy with BEV and/or hormonal agents was at the physicians’ discretion. Among the 387 included patients, the most common adverse events were anemia (61.9%, mainly grade 1), grade 3/4 neutropenia (16.5%), grade 1/2 fatigue (22.3%), and grade 1/2 neuropathy (19.6%). Dose reductions were required in 164 cycles (7.1%) and toxicity led to treatment discontinuation in 21 patients (5.4%). The median PFS and the median overall survival (OS) were 13.3 (95% CI: 11.7–14.8) and 32.3 months (95% CI: 27.7–36.9), respectively. Maintenance therapy, with hormonal agents (ET) and/or BEV, was associated with longer OS versus no maintenance therapy (47.2 versus 23.6 months; p < 0.001) in patients with hormone receptor (HR)-positive disease and BEV maintenance offered longer OS versus no maintenance in patients with HR-negative disease (52.8 versus 23.3; p = 0.023). These real-life data show that front-line BEV-based chemotherapy in HER2-negative mBC patients is an effective treatment with an acceptable toxicity profile. The potential benefit of maintenance treatment, especially ET, is important and warrants further research. MDPI 2022-02-17 /pmc/articles/PMC8871254/ /pubmed/35200604 http://dx.doi.org/10.3390/curroncol29020105 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kokkali, Stefania
Saloustros, Emmanouil
Stefanou, Dimitra
Makrantonakis, Paris
Kentepozidis, Nikolaos
Boukovinas, Ioannis
Xenidis, Nikolaos
Katsaounis, Panagiotis
Ardavanis, Alexandros
Ziras, Nikolaos
Christopoulou, Athina
Rigas, George
Kalbakis, Kostas
Vardakis, Nikolaos
Emmanouilides, Christos
Athanasiadis, Ilias
Anagnostopoulos, Athanassios
Hatzidaki, Dora
Prinarakis, Efthimios
Simopoulou, Foteini
Kotsakis, Athanasios
Georgoulias, Vassilis
Front-Line Bevacizumab plus Chemotherapy with or without Maintenance Therapy for Metastatic Breast Cancer: An Observational Study by the Hellenic Oncology Research Group
title Front-Line Bevacizumab plus Chemotherapy with or without Maintenance Therapy for Metastatic Breast Cancer: An Observational Study by the Hellenic Oncology Research Group
title_full Front-Line Bevacizumab plus Chemotherapy with or without Maintenance Therapy for Metastatic Breast Cancer: An Observational Study by the Hellenic Oncology Research Group
title_fullStr Front-Line Bevacizumab plus Chemotherapy with or without Maintenance Therapy for Metastatic Breast Cancer: An Observational Study by the Hellenic Oncology Research Group
title_full_unstemmed Front-Line Bevacizumab plus Chemotherapy with or without Maintenance Therapy for Metastatic Breast Cancer: An Observational Study by the Hellenic Oncology Research Group
title_short Front-Line Bevacizumab plus Chemotherapy with or without Maintenance Therapy for Metastatic Breast Cancer: An Observational Study by the Hellenic Oncology Research Group
title_sort front-line bevacizumab plus chemotherapy with or without maintenance therapy for metastatic breast cancer: an observational study by the hellenic oncology research group
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871254/
https://www.ncbi.nlm.nih.gov/pubmed/35200604
http://dx.doi.org/10.3390/curroncol29020105
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