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Germline Mutation Status, Pathological Complete Response, and Disease-Free Survival in Triple-Negative Breast Cancer
Author(s) -
Eric Hahnen,
Bianca Lederer,
Jan Hauke,
Sibylle Loibl,
Sandra Kröber,
Andreas Schneeweiß,
Carsten Denkert,
Peter A. Fasching,
JensUwe Blohmer,
Christian Jackisch,
Stefan Paepke,
Bernd Gerber,
Sherko Kümmel,
Christian Schem,
Guido Neidhardt,
Jens Huober,
Kerstin Rhiem,
Serban Dan Costa,
Janine Altmüller,
Claus Hanusch,
Hölger Thiele,
Volkmar Müller,
Peter Nürnberg,
Thomas Karn,
Valentiekljudova,
Michael Untch,
Gϋnter von Minckwitz,
Rita K. Schmutzler
Publication year - 2017
Publication title -
jama oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 8.846
H-Index - 99
eISSN - 2374-2445
pISSN - 2374-2437
DOI - 10.1001/jamaoncol.2017.1007
Subject(s) - medicine , carboplatin , breast cancer , oncology , triple negative breast cancer , germline mutation , taxane , regimen , brca mutation , cancer , mutation , chemotherapy , genetics , biology , cisplatin , gene
The GeparSixto trial provided evidence that the addition of neoadjuvant carboplatin to a regimen consisting of anthracycline, taxane, and bevacizumab increases pathological complete response (pCR) rates in patients with triple-negative breast cancer (TNBC). Whether BRCA1 and BRCA2 germline mutation status affects treatment outcome remains elusive.

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