Literature DB >> 30145018

Early genetic counseling and detection of CDH1 mutation in asymptomatic carriers improves survival in hereditary diffuse gastric cancer.

Maitham A Moslim1, Brandie Heald2, Chao Tu3, Carol A Burke4, R Matthew Walsh5.   

Abstract

BACKGROUND: Hereditary diffuse gastric cancer is associated with E-cadherin (CDH1) germline mutations. The implications of CDH1 mutations detected with multigene panels in those without family history of HDGC are uncertain.
METHODS: A registry of patients who underwent genetic counseling for CDH1 mutation was queried for the period 2011-2017.
RESULTS: Twenty-one patients with CDH1 mutation were identified. The most common indication for CDH1 genetic screening was family history of hereditary diffuse gastric cancer (known risk) in 10 patients (48%); 11 patients (52%), however, were diagnosed by multigene cancer panels (unknown risk). Nine of the 21 patients underwent total gastrectomy, and 5 others had metastatic gastric cancer at presentation. In the gastrectomy group, 5 of the 9 patients (56%) were known to have gastric cancer based on preoperative screening endoscopy, but final pathologic examinations indicated diffuse gastric cancer in 8 of the 9 patients. The 11 patients with unknown risk for CDH1 mutation tended to be older (median 41 vs 24 years) and more likely to have metastatic disease and to die of the disease (43% vs 29%) compared with patients with family history of hereditary diffuse gastric cancer.
CONCLUSION: CDH1 mutation-associated hereditary diffuse gastric cancer is a biologically aggressive variant of gastric cancer that appears to behave similarly in patients detected only by multigene panels. The detection of CDH1 mutation at a minimum warrants genetic counseling and preferably total gastrectomy.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2018        PMID: 30145018     DOI: 10.1016/j.surg.2018.05.059

Source DB:  PubMed          Journal:  Surgery        ISSN: 0039-6060            Impact factor:   3.982


  6 in total

Review 1.  The role of endoscopy in the management of hereditary diffuse gastric cancer syndrome.

Authors:  Shria Kumar; Jessica M Long; Gregory G Ginsberg; Bryson W Katona
Journal:  World J Gastroenterol       Date:  2019-06-21       Impact factor: 5.742

Review 2.  Case series of three patients with hereditary diffuse gastric cancer in a single family: Three case reports and review of literature.

Authors:  Masahiro Hirakawa; Kohichi Takada; Masanori Sato; Chisa Fujita; Naotaka Hayasaka; Takayuki Nobuoka; Shintaro Sugita; Aki Ishikawa; Miyako Mizukami; Hiroyuki Ohnuma; Kazuyuki Murase; Koji Miyanishi; Masayoshi Kobune; Ichiro Takemasa; Tadashi Hasegawa; Akihiro Sakurai; Junji Kato
Journal:  World J Gastroenterol       Date:  2020-11-14       Impact factor: 5.742

3.  Gastric Cancer in Aktobe Region of Western Kazakhstan from 2009 to 2018: Incidence Rates, Trends, and Five-Year Survival.

Authors:  Saule K Balmagambetova; Yerbol Z Bekmukhambetov; Anar B Tulyaeva; Yerbolat M Iztleuov; Gaziza A Smagulova; Arip K Koyshybaev; Olzhas N Urazayev; Saganaj T Djussembekov; Valeriy V Begunov; Irakli Kokhreidze
Journal:  Asian Pac J Cancer Prev       Date:  2020-06-01

Review 4.  Hereditary Diffuse Gastric Cancer: Molecular Genetics, Biological Mechanisms and Current Therapeutic Approaches.

Authors:  Lidia-Sabina Cosma; Sophie Schlosser; Hauke C Tews; Martina Müller; Arne Kandulski
Journal:  Int J Mol Sci       Date:  2022-07-15       Impact factor: 6.208

5.  Enhanced endoscopic detection of occult gastric cancer in carriers of pathogenic CDH1 variants.

Authors:  Bryan Franklin Curtin; Lauren Ann Gamble; Samuel Ali Schueler; Samantha Marilyn Ruff; Martha Quezado; Markku Miettinen; Grace-Ann Fasaye; Monica Passi; Jonathan Matthew Hernandez; Theo Heller; Christopher Koh; Jeremy Lee Davis
Journal:  J Gastroenterol       Date:  2020-11-18       Impact factor: 6.772

6.  Quadruple Multiple Primary Malignancies: Early Detection of Second Primary Malignancy by Esophagogastroduodenoscopy/Colonoscopy Is Crucial for Patients with Classic Kaposi's Sarcoma.

Authors:  Nobuyuki Maruyama; Yuko Okubo; Masato Umikawa; Akiko Matsuzaki; Akira Hokama; Fusahiro Hirano; Tessho Maruyama; Kazuhide Nishihara; Toshiyuki Nakasone; Shoko Makishi; Hiroyuki Nakamura; Naoki Yoshimi
Journal:  Diagnostics (Basel)       Date:  2020-04-14
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.