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Molecular profile of breast cancers in Guinean oncological settings

Breast cancer is a complex disease characterized by the accumulation of multiple molecular alterations giving each tumor phenotype and an own evolutionary potential. This study aimed to describe the distribution of the profile and molecular subtypes of breast cancers followed at Surgical Oncology Un...

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Autores principales: Traoré, Bangaly, Koulibaly, Moussa, Diallo, Aissatou, Bah, Malick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615767/
https://www.ncbi.nlm.nih.gov/pubmed/31312338
http://dx.doi.org/10.11604/pamj.2019.33.22.18189
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author Traoré, Bangaly
Koulibaly, Moussa
Diallo, Aissatou
Bah, Malick
author_facet Traoré, Bangaly
Koulibaly, Moussa
Diallo, Aissatou
Bah, Malick
author_sort Traoré, Bangaly
collection PubMed
description Breast cancer is a complex disease characterized by the accumulation of multiple molecular alterations giving each tumor phenotype and an own evolutionary potential. This study aimed to describe the distribution of the profile and molecular subtypes of breast cancers followed at Surgical Oncology Unit of Donka National Hospital. This was retrospective and descriptive study on cases of breast cancer in which the hormone receptor status and expression of the Her2 oncogene have been performed from 2007 to 2016. We recorded 58 cases including 56 (96.6%) women and 2 (3.4%) men. The average age was 48.2 ± 10.9. Invasive ductal carcinoma accounted for 50 (86.2%) cases. The SBR grade was II in 31(53.4%) cases, III in 21 (36.2%) cases and I in 6 (10.3%) cases. The tumor was classified as T4 in 36 (62.1%) cases; it was metastatic in 11(19.0%) cases. Estrogen receptors were positive in 29 (50.0%) cases, progesterone receptors positive in 25 (43.1%) cases, the Her2 oncogene was positive in 22 (39.3%) cases. The distribution of molecular sub-types was: 20 (34.5%) luminal A, 15 (25.9%) triple negative, 13 (22.4%) Her2 overexpressed, 8 (13.8%) luminal B and 2 (3.2%) undetermined. This preliminary study showed the poor accessibility of immunohistochemistry for the molecular diagnosis of breast cancer in our country. Luminal A subtypes and triple negatives were more common. The determination of molecular subtypes is a rational basis for hormone therapy and targeted therapy, thus personalizing the treatment of breast cancer.
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spelling pubmed-66157672019-07-16 Molecular profile of breast cancers in Guinean oncological settings Traoré, Bangaly Koulibaly, Moussa Diallo, Aissatou Bah, Malick Pan Afr Med J Case Series Breast cancer is a complex disease characterized by the accumulation of multiple molecular alterations giving each tumor phenotype and an own evolutionary potential. This study aimed to describe the distribution of the profile and molecular subtypes of breast cancers followed at Surgical Oncology Unit of Donka National Hospital. This was retrospective and descriptive study on cases of breast cancer in which the hormone receptor status and expression of the Her2 oncogene have been performed from 2007 to 2016. We recorded 58 cases including 56 (96.6%) women and 2 (3.4%) men. The average age was 48.2 ± 10.9. Invasive ductal carcinoma accounted for 50 (86.2%) cases. The SBR grade was II in 31(53.4%) cases, III in 21 (36.2%) cases and I in 6 (10.3%) cases. The tumor was classified as T4 in 36 (62.1%) cases; it was metastatic in 11(19.0%) cases. Estrogen receptors were positive in 29 (50.0%) cases, progesterone receptors positive in 25 (43.1%) cases, the Her2 oncogene was positive in 22 (39.3%) cases. The distribution of molecular sub-types was: 20 (34.5%) luminal A, 15 (25.9%) triple negative, 13 (22.4%) Her2 overexpressed, 8 (13.8%) luminal B and 2 (3.2%) undetermined. This preliminary study showed the poor accessibility of immunohistochemistry for the molecular diagnosis of breast cancer in our country. Luminal A subtypes and triple negatives were more common. The determination of molecular subtypes is a rational basis for hormone therapy and targeted therapy, thus personalizing the treatment of breast cancer. The African Field Epidemiology Network 2019-05-14 /pmc/articles/PMC6615767/ /pubmed/31312338 http://dx.doi.org/10.11604/pamj.2019.33.22.18189 Text en © Bangaly Traoré et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Series
Traoré, Bangaly
Koulibaly, Moussa
Diallo, Aissatou
Bah, Malick
Molecular profile of breast cancers in Guinean oncological settings
title Molecular profile of breast cancers in Guinean oncological settings
title_full Molecular profile of breast cancers in Guinean oncological settings
title_fullStr Molecular profile of breast cancers in Guinean oncological settings
title_full_unstemmed Molecular profile of breast cancers in Guinean oncological settings
title_short Molecular profile of breast cancers in Guinean oncological settings
title_sort molecular profile of breast cancers in guinean oncological settings
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615767/
https://www.ncbi.nlm.nih.gov/pubmed/31312338
http://dx.doi.org/10.11604/pamj.2019.33.22.18189
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