| Literature DB >> 30041945 |
Camille Tlemsani1, Eric Pasmant2, Pascaline Boudou-Rouquette3, Audrey Bellesoeur3, Julien Even4, Frédérique Larousserie5, Cécile Reyes6, David Gentien6, Jérôme Alexandre3, Michel Vidaud2, Philippe Anract4, Karen Leroy7, François Goldwasser3.
Abstract
We report the case of a patient with a BRCA2 germline mutation who developed a localized pleomorphic soft tissue sarcoma of the leg with poor prognostic features. BRCA2 germline mutations were not previously reported to be associated with pleomorphic sarcoma. BRCA2 loss-of-heterozygosity was found in the tumor, resulting in a complete BRCA2 loss-of-function. BRCA2 deficiency is associated with sensitivity to cisplatin-based chemotherapy in breast and ovarian cancer patients. We used a cisplatin-based chemotherapy. A rapid major partial response was obtained, which allowed a curative and conservative surgical resection of the sarcoma followed by adjuvant irradiation. This case illustrates that sarcoma patients may present unexpected but targetable genetic abnormalities and that BRCA2 loss-of-function may be targetable in sarcoma as it is associated with enhanced sensitivity to cisplatin. Our observation emphasizes the input of genomic medicine in clinical practice, its importance for treatment decisions, and the overlap between constitutional and somatic genetics.Entities:
Keywords: BRCA2; Cancer predisposition; Cisplatin; Genomic medicine; Pleomorphic sarcoma
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Year: 2018 PMID: 30041945 DOI: 10.1016/j.amjms.2018.04.015
Source DB: PubMed Journal: Am J Med Sci ISSN: 0002-9629 Impact factor: 2.378