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High incidence of germline BRCA mutation in patients with ER low-positive/PR low-positive/HER-2 neu negative tumors.
Sanford, Rachel A; Song, Juhee; Gutierrez-Barrera, Angelica M; Profato, Jessica; Woodson, Ashley; Litton, Jennifer Keating; Bedrosian, Isabelle; Albarracin, Constance T; Valero, Vicente; Arun, Banu.
Afiliação
  • Sanford RA; Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Song J; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Gutierrez-Barrera AM; Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Profato J; Department of Clinical Cancer Genetics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Woodson A; Department of Clinical Cancer Genetics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Litton JK; Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Bedrosian I; Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Albarracin CT; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Valero V; Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Arun B; Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer ; 121(19): 3422-7, 2015 Oct 01.
Article em En | MEDLINE | ID: mdl-26280679
ABSTRACT

BACKGROUND:

The 2015 National Comprehensive Cancer Network guidelines recommend that genetic counseling and germline BRCA mutation testing be offered to women under age 60 with triple-negative breast cancer (TNBC). As a result of the 2010 American Society of Clinical Oncology (ASCO)/College of American Pathologists (CAP) guidelines for breast cancer, patients with breast cancers that are estrogen receptor (ER) or progesterone receptor (PR) low-positive (1%-9% on immunohistochemistry) are no longer strictly considered to have TNBC and may not be referred for genetic counseling. However, the incidence of BRCA mutation in patients with hormone receptor (HR) low-positive breast cancers remains unknown, and current ASCO/CAP guidelines may result in undertesting for BRCA mutations.

METHODS:

A prospectively maintained research database of breast cancer patients evaluated at The University of Texas MD Anderson Cancer Center between 2004 and 2014 was reviewed; 314 patients were identified with HER2/neu-negative breast cancers expressing ER and PR <10% with known BRCA mutation status.

RESULTS:

Three hundred fourteen patients had breast cancers expressing ER and PR <10%; 238 (75.8%) had HR-negative cancers (<1% ER and PR), and 76 (24.2%) had HR-low-positive cancers (1%-9% ER and/or PR). Among patients with HR-negative tumors, 86 of 238 (36.1%) had a BRCA1/2 mutation, whereas in the HR-low-positive group, 30 of 76 (39.5%) had a BRCA1/2 mutation. In multivariate analysis, HR status (<1% vs 1%-9%) was not significantly associated with BRCA1/2 mutations.

CONCLUSIONS:

The incidence of BRCA1/2 mutations is similar in patients with HR-low-positive breast cancer and patients with HR-negative breast cancer. Genetic counseling and BRCA testing should be offered to patients under age 60 who have HR-low-positive breast cancers. Cancer 2015;1213435-43. © 2015 American Cancer Society.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Receptor ErbB-2 Tipo de estudo: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Receptor ErbB-2 Tipo de estudo: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article