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Early metabolic response of breast cancer to neoadjuvant endocrine therapy: comparison to morphological and pathological response

BACKGROUND: Neoadjuvant endocrine therapy (NET) has shown efficacy in terms of clinical response and surgical outcome in postmenopausal patients with estrogen receptor-positive / HER2-negative breast cancer (ER+/HER2- BC) but monitoring of tumor response is challenging. The aim of the present study...

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Autores principales: Boughdad, Sarah, Champion, Laurence, Becette, Veronique, Cherel, Pascal, Fourme, Emmanuelle, Lemonnier, Jerome, Lerebours, Florence, Alberini, Jean-Louis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986018/
https://www.ncbi.nlm.nih.gov/pubmed/31992361
http://dx.doi.org/10.1186/s40644-020-0287-4
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author Boughdad, Sarah
Champion, Laurence
Becette, Veronique
Cherel, Pascal
Fourme, Emmanuelle
Lemonnier, Jerome
Lerebours, Florence
Alberini, Jean-Louis
author_facet Boughdad, Sarah
Champion, Laurence
Becette, Veronique
Cherel, Pascal
Fourme, Emmanuelle
Lemonnier, Jerome
Lerebours, Florence
Alberini, Jean-Louis
author_sort Boughdad, Sarah
collection PubMed
description BACKGROUND: Neoadjuvant endocrine therapy (NET) has shown efficacy in terms of clinical response and surgical outcome in postmenopausal patients with estrogen receptor-positive / HER2-negative breast cancer (ER+/HER2- BC) but monitoring of tumor response is challenging. The aim of the present study was to investigate the value of an early metabolic response compared to morphological and pathological responses in this population. METHODS: This was an ancillary study of CARMINA 02, a phase II clinical trial evaluating side-by-side the efficacy of 4 to 6 months of anastrozole or fulvestrant. Positron Emission Tomography/Computed Tomography using 2-deoxy-2-[(18)F]fluoro-D-glucose (FDG-PET/CT) scans were performed at baseline (M0), early after 1 month of treatment (M1) and pre-operatively in 11 patients (74.2 yo ± 3.6). Patients were classified as early “metabolic responders” (mR) when the decrease of SUVmax was higher than 40%, and “metabolic non-responders” (mNR) otherwise. Early metabolic response was compared to morphological response (palpation, US and MRI), variation of Ki-67 index, pathological response according to the Sataloff classification and also to Preoperative Endocrine Prognostic Index (PEPI) score. It was also correlated with overall survival (OS) and recurrence-free survival (RFS). RESULTS: Tumor size measured on US and on MRI was smaller in mR than mNR, with the highest statistically significant difference at M1 (p = 0.01 and 7.1 × 10(− 5), respectively). No statistically significant difference in the variation of tumor size between M0 and M1 assessed on US or MRI was observed between mR and mNR. mR had a better clinical response: no progressive disease in mR vs 2 in mNR and 2 partial response in mR vs 1 partial response in mNR. One patient with a pre-operative complete metabolic response had the best pathological response. Pathological response did not show any statistically significant difference between mR and mNR. mR had better OS and RFS (Kaplan-Meier p = 0.08 and 0.06, respectively). All cancer-related events occurred in mNR: 3 patients died, 2 of them from progressive disease. CONCLUSIONS: FDG-PET/CT imaging could become a “surrogate marker” to monitor tumor response, especially as NET is a valuable treatment option in postmenopausal women with ER+/HER2- BC.
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spelling pubmed-69860182020-01-30 Early metabolic response of breast cancer to neoadjuvant endocrine therapy: comparison to morphological and pathological response Boughdad, Sarah Champion, Laurence Becette, Veronique Cherel, Pascal Fourme, Emmanuelle Lemonnier, Jerome Lerebours, Florence Alberini, Jean-Louis Cancer Imaging Research Article BACKGROUND: Neoadjuvant endocrine therapy (NET) has shown efficacy in terms of clinical response and surgical outcome in postmenopausal patients with estrogen receptor-positive / HER2-negative breast cancer (ER+/HER2- BC) but monitoring of tumor response is challenging. The aim of the present study was to investigate the value of an early metabolic response compared to morphological and pathological responses in this population. METHODS: This was an ancillary study of CARMINA 02, a phase II clinical trial evaluating side-by-side the efficacy of 4 to 6 months of anastrozole or fulvestrant. Positron Emission Tomography/Computed Tomography using 2-deoxy-2-[(18)F]fluoro-D-glucose (FDG-PET/CT) scans were performed at baseline (M0), early after 1 month of treatment (M1) and pre-operatively in 11 patients (74.2 yo ± 3.6). Patients were classified as early “metabolic responders” (mR) when the decrease of SUVmax was higher than 40%, and “metabolic non-responders” (mNR) otherwise. Early metabolic response was compared to morphological response (palpation, US and MRI), variation of Ki-67 index, pathological response according to the Sataloff classification and also to Preoperative Endocrine Prognostic Index (PEPI) score. It was also correlated with overall survival (OS) and recurrence-free survival (RFS). RESULTS: Tumor size measured on US and on MRI was smaller in mR than mNR, with the highest statistically significant difference at M1 (p = 0.01 and 7.1 × 10(− 5), respectively). No statistically significant difference in the variation of tumor size between M0 and M1 assessed on US or MRI was observed between mR and mNR. mR had a better clinical response: no progressive disease in mR vs 2 in mNR and 2 partial response in mR vs 1 partial response in mNR. One patient with a pre-operative complete metabolic response had the best pathological response. Pathological response did not show any statistically significant difference between mR and mNR. mR had better OS and RFS (Kaplan-Meier p = 0.08 and 0.06, respectively). All cancer-related events occurred in mNR: 3 patients died, 2 of them from progressive disease. CONCLUSIONS: FDG-PET/CT imaging could become a “surrogate marker” to monitor tumor response, especially as NET is a valuable treatment option in postmenopausal women with ER+/HER2- BC. BioMed Central 2020-01-28 /pmc/articles/PMC6986018/ /pubmed/31992361 http://dx.doi.org/10.1186/s40644-020-0287-4 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Boughdad, Sarah
Champion, Laurence
Becette, Veronique
Cherel, Pascal
Fourme, Emmanuelle
Lemonnier, Jerome
Lerebours, Florence
Alberini, Jean-Louis
Early metabolic response of breast cancer to neoadjuvant endocrine therapy: comparison to morphological and pathological response
title Early metabolic response of breast cancer to neoadjuvant endocrine therapy: comparison to morphological and pathological response
title_full Early metabolic response of breast cancer to neoadjuvant endocrine therapy: comparison to morphological and pathological response
title_fullStr Early metabolic response of breast cancer to neoadjuvant endocrine therapy: comparison to morphological and pathological response
title_full_unstemmed Early metabolic response of breast cancer to neoadjuvant endocrine therapy: comparison to morphological and pathological response
title_short Early metabolic response of breast cancer to neoadjuvant endocrine therapy: comparison to morphological and pathological response
title_sort early metabolic response of breast cancer to neoadjuvant endocrine therapy: comparison to morphological and pathological response
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986018/
https://www.ncbi.nlm.nih.gov/pubmed/31992361
http://dx.doi.org/10.1186/s40644-020-0287-4
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