Literature DB >> 33794268

Familial Burden and Other Clinical Factors Associated With Various Types of Cancer in Individuals With Lynch Syndrome.

Leah H Biller1, Miki Horiguchi2, Hajime Uno2, Chinedu Ukaegbu3, Sapna Syngal1, Matthew B Yurgelun4.   

Abstract

BACKGROUND & AIMS: Lynch syndrome (LS) is associated with increased risks of various gastrointestinal, gynecologic, genitourinary, and other cancers. Many clinical practice guidelines recommend that LS carriers' screening strategies be devised based on their family history of various cancers, in addition to age-, sex-, and gene-specific considerations. The aim of this study was to examine the association between family history and other clinical factors with LS carriers' histories of various cancers.
METHODS: Two cohorts of LS carriers were analyzed: a laboratory-based cohort of consecutively ascertained individuals undergoing germline LS testing and a clinic-based cohort of LS carriers undergoing clinical care at an academic medical center. Multivariable logistic regression was performed to assess clinical factors associated with LS carriers' histories of various cancers/neoplasms. Familial burden was defined as LS carriers' aggregate number of first-/second-degree relatives with a history of a given malignancy.
RESULTS: Multivariable analysis of the laboratory-based cohort (3828 LS carriers) identified familial burden as being incrementally associated with LS carriers' personal history of endometrial (odds ratio [OR], 1.37 per affected first-/second-degree relative; 95% confidence interval [CI], 1.21-1.56), urinary tract (OR, 2.72; 95% CI, 2.02-3.67), small bowel (OR, 3.17; 95% CI, 1.65-6.12), gastric (OR, 1.93; 95% CI, 1.24-3.02), and pancreaticobiliary cancers (OR, 2.10; 95% CI, 1.21-3.65) and sebaceous neoplasms (OR, 7.39; 95% CI, 2.71-20.15). Multivariable analysis of the clinic-based cohort (607 LS carriers) confirmed a significant association of familial burden of endometrial and urinary tract cancers.
CONCLUSIONS: Familial burden - in addition to age, sex, and specific LS gene - should be used to assess LS carriers' risks of specific cancers and guide decision-making about organ-specific surveillance.
Copyright © 2021 AGA Institute. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Extracolonic; HNPCC; Screening

Mesh:

Substances:

Year:  2021        PMID: 33794268      PMCID: PMC9115644          DOI: 10.1053/j.gastro.2021.03.039

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   33.883


  23 in total

1.  Familial risk-colorectal cancer: ESMO Clinical Practice Guidelines.

Authors:  J Balmaña; F Balaguer; A Cervantes; D Arnold
Journal:  Ann Oncol       Date:  2013-06-27       Impact factor: 32.976

2.  Hereditary gastrointestinal cancers: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up†.

Authors:  N Stjepanovic; L Moreira; F Carneiro; F Balaguer; A Cervantes; J Balmaña; E Martinelli
Journal:  Ann Oncol       Date:  2019-10-01       Impact factor: 32.976

3.  Value of upper gastrointestinal endoscopy for gastric cancer surveillance in patients with Lynch syndrome.

Authors:  Swetlana Ladigan-Badura; Deepak B Vangala; Christoph Engel; Karolin Bucksch; Robert Hueneburg; Claudia Perne; Jacob Nattermann; Verena Steinke-Lange; Nils Rahner; Hans K Schackert; Jürgen Weitz; Matthias Kloor; Judith Kuhlkamp; Huu Phuc Nguyen; Gabriela Moeslein; Christian Strassburg; Monika Morak; Elke Holinski-Feder; Reinhard Buettner; Stefan Aretz; Markus Loeffler; Wolff Schmiegel; Christian Pox; Karsten Schulmann
Journal:  Int J Cancer       Date:  2020-10-13       Impact factor: 7.396

4.  Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.

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Journal:  J Clin Oncol       Date:  2014-12-01       Impact factor: 44.544

5.  Prophylactic surgery to reduce the risk of gynecologic cancers in the Lynch syndrome.

Authors:  Kathleen M Schmeler; Henry T Lynch; Lee-may Chen; Mark F Munsell; Pamela T Soliman; Mary Beth Clark; Molly S Daniels; Kristin G White; Stephanie G Boyd-Rogers; Peggy G Conrad; Kathleen Y Yang; Mary M Rubin; Charlotte C Sun; Brian M Slomovitz; David M Gershenson; Karen H Lu
Journal:  N Engl J Med       Date:  2006-01-19       Impact factor: 91.245

6.  Genomic and transcriptomic heterogeneity of colorectal tumours arising in Lynch syndrome.

Authors:  Hans Binder; Lydia Hopp; Michal R Schweiger; Steve Hoffmann; Frank Jühling; Martin Kerick; Bernd Timmermann; Susann Siebert; Christina Grimm; Lilit Nersisyan; Arsen Arakelyan; Maria Herberg; Peter Buske; Henry Loeffler-Wirth; Maciej Rosolowski; Christoph Engel; Jens Przybilla; Martin Peifer; Nicolaus Friedrichs; Gabriela Moeslein; Margarete Odenthal; Michelle Hussong; Sophia Peters; Stefanie Holzapfel; Jacob Nattermann; Robert Hueneburg; Wolff Schmiegel; Brigitte Royer-Pokora; Stefan Aretz; Michael Kloth; Matthias Kloor; Reinhard Buettner; Jörg Galle; Markus Loeffler
Journal:  J Pathol       Date:  2017-09-05       Impact factor: 7.996

7.  Guidelines for the management of hereditary colorectal cancer from the British Society of Gastroenterology (BSG)/Association of Coloproctology of Great Britain and Ireland (ACPGBI)/United Kingdom Cancer Genetics Group (UKCGG).

Authors:  Kevin J Monahan; Nicola Bradshaw; Sunil Dolwani; Bianca Desouza; Malcolm G Dunlop; James E East; Mohammad Ilyas; Asha Kaur; Fiona Lalloo; Andrew Latchford; Matthew D Rutter; Ian Tomlinson; Huw J W Thomas; James Hill
Journal:  Gut       Date:  2019-11-28       Impact factor: 23.059

8.  Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer.

Authors:  Aung Ko Win; Mark A Jenkins; James G Dowty; Antonis C Antoniou; Andrew Lee; Graham G Giles; Daniel D Buchanan; Mark Clendenning; Christophe Rosty; Dennis J Ahnen; Stephen N Thibodeau; Graham Casey; Steven Gallinger; Loïc Le Marchand; Robert W Haile; John D Potter; Yingye Zheng; Noralane M Lindor; Polly A Newcomb; John L Hopper; Robert J MacInnis
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2016-10-31       Impact factor: 4.254

9.  Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database.

Authors:  Pål Møller; Toni T Seppälä; Inge Bernstein; Elke Holinski-Feder; Paulo Sala; D Gareth Evans; Annika Lindblom; Finlay Macrae; Ignacio Blanco; Rolf H Sijmons; Jacqueline Jeffries; Hans F A Vasen; John Burn; Sigve Nakken; Eivind Hovig; Einar Andreas Rødland; Kukatharmini Tharmaratnam; Wouter H de Vos Tot Nederveen Cappel; James Hill; Juul T Wijnen; Mark A Jenkins; Kate Green; Fiona Lalloo; Lone Sunde; Miriam Mints; Lucio Bertario; Marta Pineda; Matilde Navarro; Monika Morak; Laura Renkonen-Sinisalo; Mev Dominguez Valentin; Ian M Frayling; John-Paul Plazzer; Kirsi Pylvanainen; Maurizio Genuardi; Jukka-Pekka Mecklin; Gabriela Moeslein; Julian R Sampson; Gabriel Capella
Journal:  Gut       Date:  2017-07-28       Impact factor: 23.059

10.  Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial.

Authors:  John Burn; Harsh Sheth; Faye Elliott; Lynn Reed; Finlay Macrae; Jukka-Pekka Mecklin; Gabriela Möslein; Fiona E McRonald; Lucio Bertario; D Gareth Evans; Anne-Marie Gerdes; Judy W C Ho; Annika Lindblom; Patrick J Morrison; Jem Rashbass; Raj Ramesar; Toni Seppälä; Huw J W Thomas; Kirsi Pylvänäinen; Gillian M Borthwick; John C Mathers; D Timothy Bishop
Journal:  Lancet       Date:  2020-06-13       Impact factor: 79.321

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