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Ki-67 biomarker in breast cancer of Indian women

BACKGROUND: Biological markers that reliably predict clinical or pathological response to primary systemic therapy early during a course of chemotherapy may have considerable clinical potential. AIMS: Aims of study to evaluated changes in Ki-67 (MIB-1) labeling index and apoptotic index (AI) before,...

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Autores principales: Patil, Amit V., Singhai, Rajeev, Bhamre, Rahul S., Patil, Vinayak W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3336898/
https://www.ncbi.nlm.nih.gov/pubmed/22540077
http://dx.doi.org/10.4297/najms.2011.3119
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author Patil, Amit V.
Singhai, Rajeev
Bhamre, Rahul S.
Patil, Vinayak W.
author_facet Patil, Amit V.
Singhai, Rajeev
Bhamre, Rahul S.
Patil, Vinayak W.
author_sort Patil, Amit V.
collection PubMed
description BACKGROUND: Biological markers that reliably predict clinical or pathological response to primary systemic therapy early during a course of chemotherapy may have considerable clinical potential. AIMS: Aims of study to evaluated changes in Ki-67 (MIB-1) labeling index and apoptotic index (AI) before, during, and after neoadjuvant anthracycline chemotherapy in breast cancer in Indian women. MATERIALS AND METHODS: Breast cancer tissues were collected from Grant Medical College and Sir J.J. Group of Hospitals, Mumbai, India. Twenty-seven patients receiving neoadjuvant FEC (5-fluorouracil, epirubicin, and cyclophosphamide) chemotherapy for operable breast cancer underwent repeat core biopsy after 21 days of treatment. RESULTS: The objective clinical response rate was 56%. Eight patients (31%) achieved a pathological response by histopathological criteria; two patients had a near-complete pathological response. Increased day-21 AI was a statistically significant predictor of pathological response (p = 0.049). A strong trend for predicting pathological response was seen with higher Ki-67 indices at day 21 and AI at surgery (p = 0.06 and 0.06, respectively). CONCLUSION: The clinical utility of early changes in biological marker expression during chemotherapy remains unclear. Until further prospectively validated evidence confirming the reliability of predictive biomarkers is available, clinical decision-making should not be based upon individual biological tumor biomarker profiles.
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spelling pubmed-33368982012-04-26 Ki-67 biomarker in breast cancer of Indian women Patil, Amit V. Singhai, Rajeev Bhamre, Rahul S. Patil, Vinayak W. N Am J Med Sci Original Article BACKGROUND: Biological markers that reliably predict clinical or pathological response to primary systemic therapy early during a course of chemotherapy may have considerable clinical potential. AIMS: Aims of study to evaluated changes in Ki-67 (MIB-1) labeling index and apoptotic index (AI) before, during, and after neoadjuvant anthracycline chemotherapy in breast cancer in Indian women. MATERIALS AND METHODS: Breast cancer tissues were collected from Grant Medical College and Sir J.J. Group of Hospitals, Mumbai, India. Twenty-seven patients receiving neoadjuvant FEC (5-fluorouracil, epirubicin, and cyclophosphamide) chemotherapy for operable breast cancer underwent repeat core biopsy after 21 days of treatment. RESULTS: The objective clinical response rate was 56%. Eight patients (31%) achieved a pathological response by histopathological criteria; two patients had a near-complete pathological response. Increased day-21 AI was a statistically significant predictor of pathological response (p = 0.049). A strong trend for predicting pathological response was seen with higher Ki-67 indices at day 21 and AI at surgery (p = 0.06 and 0.06, respectively). CONCLUSION: The clinical utility of early changes in biological marker expression during chemotherapy remains unclear. Until further prospectively validated evidence confirming the reliability of predictive biomarkers is available, clinical decision-making should not be based upon individual biological tumor biomarker profiles. Medknow Publications & Media Pvt Ltd 2011-03 /pmc/articles/PMC3336898/ /pubmed/22540077 http://dx.doi.org/10.4297/najms.2011.3119 Text en Copyright: © North American Journal of Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Patil, Amit V.
Singhai, Rajeev
Bhamre, Rahul S.
Patil, Vinayak W.
Ki-67 biomarker in breast cancer of Indian women
title Ki-67 biomarker in breast cancer of Indian women
title_full Ki-67 biomarker in breast cancer of Indian women
title_fullStr Ki-67 biomarker in breast cancer of Indian women
title_full_unstemmed Ki-67 biomarker in breast cancer of Indian women
title_short Ki-67 biomarker in breast cancer of Indian women
title_sort ki-67 biomarker in breast cancer of indian women
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3336898/
https://www.ncbi.nlm.nih.gov/pubmed/22540077
http://dx.doi.org/10.4297/najms.2011.3119
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