PURPOSE: To develop recommendations for management of patients with breast cancer (BC) with germline mutations in BC susceptibility genes. METHODS: The American Society of Clinical Oncology, American Society for Radiation Oncology, and Society of Surgical Oncology convened an Expert Panel to develop recommendations based on a systematic review of the literature and a formal consensus process. RESULTS: Fifty-eight articles met eligibility criteria and formed the evidentiary basis for the local therapy recommendations; six randomized controlled trials of systemic therapy met eligibility criteria. RECOMMENDATIONS: Patients with newly diagnosed BC and BRCA1/2 mutations may be considered for breast-conserving therapy (BCT), with local control of...
Hereditary breast cancers, mainly due to BRCA1 and BRCA2 mutations, account for only 5–10% of this d...
To access publisher's full text version of this article click on the hyperlink belowAn international...
Protocols for activity aiming at early diagnosis and treatment of inherited breast or breast-ovarian...
Mutations due to hereditary related genes such as BRCA1, BRCA2, TP53 and PTEN confer greater risk of...
Carol Forbes,1 Debra Fayter,1 Shelley de Kock,2 Ruben GW Quek3 1Department of Reviews, Kleijnen Syst...
Sarah Edaily, Hikmat Abdel-Razeq Department of Internal Medicine, King Hussein Cancer Center, Amman,...
Hereditary breast cancer occurs in 5–20 % of cases and it is associated with inherited mutations in ...
BRCA1/2-related breast cancers (BC) can be considered a separate entity compared to sporadic ones. C...
The identification that breast cancer is hereditary was first described in the nineteenth century. W...
Abstract Approximately, 7 % of all breast cancers (BC) and 11–15 % of ovarian cancers (OC) are assoc...
Approximately 5% to 10% of all breast cancers are hereditary; many of which are caused by pathogenic...
© 2019 American Medical Association. All rights reserved. Importance: Potentially harmful mutations ...
Force (USPSTF) recommendation on genetic risk assessment and BRCA mutation testing for breast and ov...
Importance: Potentially harmful mutations of the breast cancer susceptibility 1 and 2 genes (BRCA1/2...
ImportancePotentially harmful mutations of the breast cancer susceptibility 1 and 2 genes (BRCA1/2) ...
Hereditary breast cancers, mainly due to BRCA1 and BRCA2 mutations, account for only 5–10% of this d...
To access publisher's full text version of this article click on the hyperlink belowAn international...
Protocols for activity aiming at early diagnosis and treatment of inherited breast or breast-ovarian...
Mutations due to hereditary related genes such as BRCA1, BRCA2, TP53 and PTEN confer greater risk of...
Carol Forbes,1 Debra Fayter,1 Shelley de Kock,2 Ruben GW Quek3 1Department of Reviews, Kleijnen Syst...
Sarah Edaily, Hikmat Abdel-Razeq Department of Internal Medicine, King Hussein Cancer Center, Amman,...
Hereditary breast cancer occurs in 5–20 % of cases and it is associated with inherited mutations in ...
BRCA1/2-related breast cancers (BC) can be considered a separate entity compared to sporadic ones. C...
The identification that breast cancer is hereditary was first described in the nineteenth century. W...
Abstract Approximately, 7 % of all breast cancers (BC) and 11–15 % of ovarian cancers (OC) are assoc...
Approximately 5% to 10% of all breast cancers are hereditary; many of which are caused by pathogenic...
© 2019 American Medical Association. All rights reserved. Importance: Potentially harmful mutations ...
Force (USPSTF) recommendation on genetic risk assessment and BRCA mutation testing for breast and ov...
Importance: Potentially harmful mutations of the breast cancer susceptibility 1 and 2 genes (BRCA1/2...
ImportancePotentially harmful mutations of the breast cancer susceptibility 1 and 2 genes (BRCA1/2) ...
Hereditary breast cancers, mainly due to BRCA1 and BRCA2 mutations, account for only 5–10% of this d...
To access publisher's full text version of this article click on the hyperlink belowAn international...
Protocols for activity aiming at early diagnosis and treatment of inherited breast or breast-ovarian...