Skip to Main Content (Press Enter)

Logo UNISR
  • ×
  • Home
  • People
  • Outputs
  • Organizations
  • Expertise & Skills

UNIFIND
Logo UNISR

|

UNIFIND

unisr.it
  • ×
  • Home
  • People
  • Outputs
  • Organizations
  • Expertise & Skills
  1. Outputs

Germline testing and genetic counseling in biliary tract cancer: an operative proposal to improve the state of art

Academic Article
Publication Date:
2024
Short description:
Germline testing and genetic counseling in biliary tract cancer: an operative proposal to improve the state of art / Rimini, M., Presi, S., Pipitone, G.B., Russo Raucci, A., Ratti, F., Della Corte, A., Pedica, F., Vanella, G., Tonon, G., Burgio, V., Vitiello, F., Rossari, F., Amadeo, E., Maria Giulia, C., Pecciarini, L., Arcidiacono, P.G., Falcinelli, F., Cascinu, S., De Cobelli, F., Aldrighetti, L., et al.. - In: EXPERT REVIEW OF GASTROENTEROLOGY & HEPATOLOGY. - ISSN 1747-4124. - 18:4-5(2024), pp. 141-146. [10.1080/17474124.2024.2337000]
abstract:
Introduction: A genetic predisposition seems to be involved in biliary tract cancer, but the prevalence of germline mutations in BTC remains unclear, and the therapeutic role of the germline pathologic variants is still unknown. Area covered: The aim of the present work is to systematically review the data available on the hereditary predisposition of biliary tract cancer by a specific research on PubMed, in order to highlight the most important critical points and to define the current possible role of germinal testing and genetic counseling in this setting of patients. Expert opinion: Basing on data already available, we decided to start in our institution a specific genetic protocol focused on biliary tract cancer patients, which includes genetic counseling and, if indicated, germline test. The inclusion criteria are: 1) Patient with personal history of oncologic disease other than BTC, 2) Patient with familiar history of oncologic disease (considering relatives of first and second grade), 3) Patient with <= 50 years old, 4) Patient presenting a somatic mutation in genes involved in DNA damage repair pathways and mismatch repair. The aim of the presented protocol is to identify germline pathogenic variants with prophylactic and therapeutic impact, and to collect and integrate a significant amount of clinical, familial, somatic, and genetic data.
Iris type:
1.1 Articolo in rivista
List of contributors:
Rimini, Margherita; Presi, Silvia; Pipitone, Giovanni Battista; Russo Raucci, Annalisa; Ratti, Francesca; Della Corte, Angelo; Pedica, Federica; Vanella, Giuseppe; Tonon, Giovanni; Burgio, Valentina; Vitiello, Francesco; Rossari, Federico; Amadeo, Elisabeth; Maria Giulia, Cangi; Pecciarini, Lorenza; Arcidiacono, Paolo Giorgio; Falcinelli, Francesca; Cascinu, Stefano; De Cobelli, Francesco; Aldrighetti, Luca; Patricelli, Maria Grazia; Carrera, Paola; Casadei-Gardini, Andrea
Authors of the University:
ARCIDIACONO PAOLO GIORGIO
CASADEI GARDINI ANDREA
CASCINU STEFANO
DE COBELLI FRANCESCO
PEDICA FEDERICA
RATTI FRANCESCA
RIMINI MARGHERITA
TONON GIOVANNI
Handle:
https://iris.unisr.it/handle/20.500.11768/159337
Published in:
EXPERT REVIEW OF GASTROENTEROLOGY & HEPATOLOGY
Journal
  • Overview

Overview

URL

https://www.tandfonline.com/doi/full/10.1080/17474124.2024.2337000?scroll=top&needAccess=true
  • Use of cookies

Powered by VIVO | Designed by Cineca | 26.6.1.0