Literature DB >> 30041945

BRCA2 Loss-of-Function and High Sensitivity to Cisplatin-Based Chemotherapy in a Patient With a Pleomorphic Soft Tissue Sarcoma: Effect of Genomic Medicine.

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.
Copyright © 2018 Southern Society for Clinical Investigation. Published by Elsevier Inc. All rights reserved.

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


  1 in total

1.  Osteosarcoma without prior retinoblastoma related to RB1 low-penetrance germline pathogenic variants: A novel type of RB1-related hereditary predisposition syndrome?

Authors:  Marion Imbert-Bouteille; Marion Gauthier-Villars; Dominique Leroux; Isabelle Meunier; Isabelle Aerts; Livia Lumbroso-Le Rouic; Sophie Lejeune; Capucine Delnatte; Caroline Abadie; Pascal Pujol; Claude Houdayer; Carole Corsini
Journal:  Mol Genet Genomic Med       Date:  2019-09-30       Impact factor: 2.183

  1 in total

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