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Better overall survival in patients who achieve pathological complete response after neoadjuvant chemotherapy for breast cancer in a Chilean public hospital

INTRODUCTION: There is extensive evidence associating the response to neoadjuvant chemotherapy (NeoCT) with breast cancer (BC) survival. However, to the author’s knowledge, there is no published data in Chile. The objective of the study is to evaluate whether achieving pathological complete response...

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Autores principales: Acevedo, Francisco, Petric, Militza, Walbaum, Benjamin, Robin, Julieta, Legorburu, Luisa, Murature, Geraldine, Guerra, Constanza, Navarro, Marisel, Canovas, María José, Sanchez, Cesar, Vargas, Lorena, Manzor, Manuel, Peña, José, Muñiz, Sabrina, Veglia, Paulina, Cartes, Raúl, Martinez, Raúl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987490/
https://www.ncbi.nlm.nih.gov/pubmed/33777178
http://dx.doi.org/10.3332/ecancer.2021.1185
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author Acevedo, Francisco
Petric, Militza
Walbaum, Benjamin
Robin, Julieta
Legorburu, Luisa
Murature, Geraldine
Guerra, Constanza
Navarro, Marisel
Canovas, María José
Sanchez, Cesar
Vargas, Lorena
Manzor, Manuel
Peña, José
Muñiz, Sabrina
Veglia, Paulina
Cartes, Raúl
Martinez, Raúl
author_facet Acevedo, Francisco
Petric, Militza
Walbaum, Benjamin
Robin, Julieta
Legorburu, Luisa
Murature, Geraldine
Guerra, Constanza
Navarro, Marisel
Canovas, María José
Sanchez, Cesar
Vargas, Lorena
Manzor, Manuel
Peña, José
Muñiz, Sabrina
Veglia, Paulina
Cartes, Raúl
Martinez, Raúl
author_sort Acevedo, Francisco
collection PubMed
description INTRODUCTION: There is extensive evidence associating the response to neoadjuvant chemotherapy (NeoCT) with breast cancer (BC) survival. However, to the author’s knowledge, there is no published data in Chile. The objective of the study is to evaluate whether achieving pathological complete response (pCR) after NeoCT is associated with greater survival and lower risk of recurrence in a Chilean Public Health Service. METHODS: Retrospective analysis of a database. Patients with a diagnosis of Stages I–III BC who received NeoCT between 2009 and 2019 were included. Clinical and pathological information were extracted from the clinical records. BC subtypes were defined using hormone receptor (HR) information (HR: oestrogen and/or progesterone) and epidermal growth factor type 2 (HER2), being divided into four groups: HR+/HER2−, HR+/HER2+, HR−/HER2+, HR-/HER2−. pCR was defined as the absence of invasive cancer in the breast and axilla (ypT0/is N0) after NeoCT. RESULTS: Of 3,092 patients, 17.2% received NeoCT. Of these, 40.2% corresponded to HR+/HER2−, 20.9% HR+/HER2+, 18.2% HR−/HER2+ and 20.7% HR−/HER2−. Overall, 24.8% achieved pCR, being the lowest for HR+/HER2− (10.3%) and the highest for HR−/HER2+ (53.2%). In the multivariable analysis, family history, HER2+ and type of chemotherapy were associated with a greater probability of pCR. With a median follow-up of 40 months, the overall survival and metastasis-free survival (MFS) at 3 years were greater for the group with pCR compared to that which did not achieve it (90.5% versus 76.7%, p = 0.03 and 88.5% versus 71.4%, p = 0.003, respectively). The multivariable analysis confirmed this finding. Brain MFS was similar in both groups. CONCLUSION: NeoCT is associated with greater pCR in aggressive BC subtypes. In those, achieving pCR was associated with better survival in our study. To the author’s knowledge, this is the first study which evaluates the relation between pCR and BC subtypes in a Chilean public hospital.
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spelling pubmed-79874902021-03-26 Better overall survival in patients who achieve pathological complete response after neoadjuvant chemotherapy for breast cancer in a Chilean public hospital Acevedo, Francisco Petric, Militza Walbaum, Benjamin Robin, Julieta Legorburu, Luisa Murature, Geraldine Guerra, Constanza Navarro, Marisel Canovas, María José Sanchez, Cesar Vargas, Lorena Manzor, Manuel Peña, José Muñiz, Sabrina Veglia, Paulina Cartes, Raúl Martinez, Raúl Ecancermedicalscience Research INTRODUCTION: There is extensive evidence associating the response to neoadjuvant chemotherapy (NeoCT) with breast cancer (BC) survival. However, to the author’s knowledge, there is no published data in Chile. The objective of the study is to evaluate whether achieving pathological complete response (pCR) after NeoCT is associated with greater survival and lower risk of recurrence in a Chilean Public Health Service. METHODS: Retrospective analysis of a database. Patients with a diagnosis of Stages I–III BC who received NeoCT between 2009 and 2019 were included. Clinical and pathological information were extracted from the clinical records. BC subtypes were defined using hormone receptor (HR) information (HR: oestrogen and/or progesterone) and epidermal growth factor type 2 (HER2), being divided into four groups: HR+/HER2−, HR+/HER2+, HR−/HER2+, HR-/HER2−. pCR was defined as the absence of invasive cancer in the breast and axilla (ypT0/is N0) after NeoCT. RESULTS: Of 3,092 patients, 17.2% received NeoCT. Of these, 40.2% corresponded to HR+/HER2−, 20.9% HR+/HER2+, 18.2% HR−/HER2+ and 20.7% HR−/HER2−. Overall, 24.8% achieved pCR, being the lowest for HR+/HER2− (10.3%) and the highest for HR−/HER2+ (53.2%). In the multivariable analysis, family history, HER2+ and type of chemotherapy were associated with a greater probability of pCR. With a median follow-up of 40 months, the overall survival and metastasis-free survival (MFS) at 3 years were greater for the group with pCR compared to that which did not achieve it (90.5% versus 76.7%, p = 0.03 and 88.5% versus 71.4%, p = 0.003, respectively). The multivariable analysis confirmed this finding. Brain MFS was similar in both groups. CONCLUSION: NeoCT is associated with greater pCR in aggressive BC subtypes. In those, achieving pCR was associated with better survival in our study. To the author’s knowledge, this is the first study which evaluates the relation between pCR and BC subtypes in a Chilean public hospital. Cancer Intelligence 2021-02-11 /pmc/articles/PMC7987490/ /pubmed/33777178 http://dx.doi.org/10.3332/ecancer.2021.1185 Text en © the authors; licensee ecancermedicalscience. 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), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Acevedo, Francisco
Petric, Militza
Walbaum, Benjamin
Robin, Julieta
Legorburu, Luisa
Murature, Geraldine
Guerra, Constanza
Navarro, Marisel
Canovas, María José
Sanchez, Cesar
Vargas, Lorena
Manzor, Manuel
Peña, José
Muñiz, Sabrina
Veglia, Paulina
Cartes, Raúl
Martinez, Raúl
Better overall survival in patients who achieve pathological complete response after neoadjuvant chemotherapy for breast cancer in a Chilean public hospital
title Better overall survival in patients who achieve pathological complete response after neoadjuvant chemotherapy for breast cancer in a Chilean public hospital
title_full Better overall survival in patients who achieve pathological complete response after neoadjuvant chemotherapy for breast cancer in a Chilean public hospital
title_fullStr Better overall survival in patients who achieve pathological complete response after neoadjuvant chemotherapy for breast cancer in a Chilean public hospital
title_full_unstemmed Better overall survival in patients who achieve pathological complete response after neoadjuvant chemotherapy for breast cancer in a Chilean public hospital
title_short Better overall survival in patients who achieve pathological complete response after neoadjuvant chemotherapy for breast cancer in a Chilean public hospital
title_sort better overall survival in patients who achieve pathological complete response after neoadjuvant chemotherapy for breast cancer in a chilean public hospital
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987490/
https://www.ncbi.nlm.nih.gov/pubmed/33777178
http://dx.doi.org/10.3332/ecancer.2021.1185
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