Literature DB >> 33839100

Gene-Specific Variation in Colorectal Cancer Surveillance Strategies for Lynch Syndrome.

Fay Kastrinos1, Myles A Ingram2, Elisabeth R Silver2, Aaron Oh2, Monika Laszkowska3, Anil K Rustgi3, Chin Hur4.   

Abstract

BACKGROUND AND AIMS: Lynch syndrome is associated with pathogenic variants in 4 mismatch repair (MMR) genes that increase lifetime risk of colorectal cancer. Guidelines recommend intensive colorectal cancer surveillance with colonoscopy every 1-2 years starting at age 25 years for all carriers of Lynch syndrome-associated variants, regardless of gene product. We constructed a simulation model to analyze the effects of different ages of colonoscopy initiation and surveillance intervals for each MMR gene (MLH1, MSH2, MSH6, and PMS2) on colorectal cancer incidence and mortality, quality-adjusted life-years, and cost.
METHODS: Using published literature, we developed a Markov simulation model of Lynch syndrome progression for patients with each MMR variant. The model simulated clinical trials of Lynch syndrome carriers, varying age of colonoscopy initiation (5-year increments from 25-40 years), and surveillance intervals (1-5 years). We assessed the optimal strategy for each gene, defined as the strategy with the highest quality-adjusted life-years and incremental cost-effectiveness ratio below a $100,000 willingness-to-pay threshold.
RESULTS: Optimal surveillance for patients with pathogenic variants in the MLH1 and MSH2 genes was colonoscopy starting at age 25 years, with 1- to 2-year surveillance intervals. Initiating colonoscopy at age 35 and 40 years, with 3-year intervals, was cost-effective for patients with pathogenic variants in MSH6 or PMS2, respectively.
CONCLUSIONS: We developed a simulation model to select optimal surveillance starting ages and intervals for patients with Lynch syndrome based on MMR variant. The model supports recommendations for intensive surveillance of patients with Lynch syndrome-associated variants in MLH1 or MSH2. However, for patients with Lynch syndrome-associated variants of MSH6 or PMS2, later initiation of surveillance at 35 and 40 years, respectively, and at 3-year intervals, can be considered.
Copyright © 2021 AGA Institute. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Colorectal Cancer; Cost-Effectiveness; Genetic Cancer Syndromes; Surveillance

Mesh:

Substances:

Year:  2021        PMID: 33839100      PMCID: PMC9330543          DOI: 10.1053/j.gastro.2021.04.010

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


  40 in total

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2.  United States Life Tables, 2016.

Authors:  Elizabeth Arias; Jiaquan Xu; Kenneth D Kochanek
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3.  Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome.

Authors:  Christoph Engel; Aysel Ahadova; Toni T Seppälä; Stefan Aretz; Marloes Bigirwamungu-Bargeman; Hendrik Bläker; Karolin Bucksch; Reinhard Büttner; Wouter T de Vos Tot Nederveen Cappel; Volker Endris; Elke Holinski-Feder; Stefanie Holzapfel; Robert Hüneburg; Maarten A J M Jacobs; Jan J Koornstra; Alexandra M Langers; Anna Lepistö; Monika Morak; Gabriela Möslein; Päivi Peltomäki; Kirsi Pylvänäinen; Nils Rahner; Laura Renkonen-Sinisalo; Karsten Schulmann; Verena Steinke-Lange; Albrecht Stenzinger; Christian P Strassburg; Paul C van de Meeberg; Mariette van Kouwen; Monique van Leerdam; Deepak B Vangala; Juda Vecht; Marie-Louise Verhulst; Magnus von Knebel Doeberitz; Jürgen Weitz; Silke Zachariae; Markus Loeffler; Jukka-Pekka Mecklin; Matthias Kloor; Hans F Vasen
Journal:  Gastroenterology       Date:  2020-01-08       Impact factor: 22.682

4.  Yield of Lynch Syndrome Surveillance for Patients With Pathogenic Variants in DNA Mismatch Repair Genes.

Authors:  Anne Goverde; Ellis L Eikenboom; Ellemieke L Viskil; Marco J Bruno; Michael Doukas; Winand N M Dinjens; Erik Jan Dubbink; Ans M W van den Ouweland; Robert M W Hofstra; Anja Wagner; Manon C W Spaander
Journal:  Clin Gastroenterol Hepatol       Date:  2019-08-27       Impact factor: 11.382

5.  Calculation of risk of colorectal and endometrial cancer among patients with Lynch syndrome.

Authors:  Elena Stoffel; Bhramar Mukherjee; Victoria M Raymond; Nabihah Tayob; Fay Kastrinos; Jennifer Sparr; Fei Wang; Prathap Bandipalliam; Sapna Syngal; Stephen B Gruber
Journal:  Gastroenterology       Date:  2009-07-18       Impact factor: 22.682

6.  Screening and surveillance in hereditary gastrointestinal cancers: Recommendations from the European Society of Digestive Oncology (ESDO) expert discussion at the 20th European Society for Medical Oncology (ESMO)/World Congress on Gastrointestinal Cancer, Barcelona, June 2018.

Authors:  Deepak B Vangala; Estelle Cauchin; Judith Balmaña; Lucian Wyrwicz; Eric van Cutsem; Ulrich Güller; Antoni Castells; Fatima Carneiro; Pascal Hammel; Michel Ducreux; Jean-Luc van Laethem; Tamara Matysiak-Budnik; Wolff Schmiegel
Journal:  Eur J Cancer       Date:  2018-10-18       Impact factor: 9.162

7.  An economic viewpoint on alternative strategies for identifying persons with hereditary nonpolyposis colorectal cancer.

Authors:  Scott D Ramsey; Wylie Burke; Lauren Clarke
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8.  Cancer Risks for PMS2-Associated Lynch Syndrome.

Authors:  Sanne W Ten Broeke; Heleen M van der Klift; Carli M J Tops; Stefan Aretz; Inge Bernstein; Daniel D Buchanan; Albert de la Chapelle; Gabriel Capella; Mark Clendenning; Christoph Engel; Steven Gallinger; Encarna Gomez Garcia; Jane C Figueiredo; Robert Haile; Heather L Hampel; John L Hopper; Nicoline Hoogerbrugge; Magnus von Knebel Doeberitz; Loic Le Marchand; Tom G W Letteboer; Mark A Jenkins; Annika Lindblom; Noralane M Lindor; Arjen R Mensenkamp; Pål Møller; Polly A Newcomb; Theo A M van Os; Rachel Pearlman; Marta Pineda; Nils Rahner; Egbert J W Redeker; Maran J W Olderode-Berends; Christophe Rosty; Hans K Schackert; Rodney Scott; Leigha Senter; Liesbeth Spruijt; Verena Steinke-Lange; Manon Suerink; Stephen Thibodeau; Yvonne J Vos; Anja Wagner; Ingrid Winship; Frederik J Hes; Hans F A Vasen; Juul T Wijnen; Maartje Nielsen; Aung Ko Win
Journal:  J Clin Oncol       Date:  2018-08-30       Impact factor: 50.717

9.  Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.

Authors:  Mev Dominguez-Valentin; Julian R Sampson; Toni T Seppälä; Sanne W Ten Broeke; John-Paul Plazzer; Sigve Nakken; Christoph Engel; Stefan Aretz; Mark A Jenkins; Lone Sunde; Inge Bernstein; Gabriel Capella; Francesc Balaguer; Huw Thomas; D Gareth Evans; John Burn; Marc Greenblatt; Eivind Hovig; Wouter H de Vos Tot Nederveen Cappel; Rolf H Sijmons; Lucio Bertario; Maria Grazia Tibiletti; Giulia Martina Cavestro; Annika Lindblom; Adriana Della Valle; Francisco Lopez-Köstner; Nathan Gluck; Lior H Katz; Karl Heinimann; Carlos A Vaccaro; Reinhard Büttner; Heike Görgens; Elke Holinski-Feder; Monika Morak; Stefanie Holzapfel; Robert Hüneburg; Magnus von Knebel Doeberitz; Markus Loeffler; Nils Rahner; Hans K Schackert; Verena Steinke-Lange; Wolff Schmiegel; Deepak Vangala; Kirsi Pylvänäinen; Laura Renkonen-Sinisalo; John L Hopper; Aung Ko Win; Robert W Haile; Noralane M Lindor; Steven Gallinger; Loïc Le Marchand; Polly A Newcomb; Jane C Figueiredo; Stephen N Thibodeau; Karin Wadt; Christina Therkildsen; Henrik Okkels; Zohreh Ketabi; Leticia Moreira; Ariadna Sánchez; Miquel Serra-Burriel; Marta Pineda; Matilde Navarro; Ignacio Blanco; Kate Green; Fiona Lalloo; Emma J Crosbie; James Hill; Oliver G Denton; Ian M Frayling; Einar Andreas Rødland; Hans Vasen; Miriam Mints; Florencia Neffa; Patricia Esperon; Karin Alvarez; Revital Kariv; Guy Rosner; Tamara Alejandra Pinero; María Laura Gonzalez; Pablo Kalfayan; Douglas Tjandra; Ingrid M Winship; Finlay Macrae; Gabriela Möslein; Jukka-Pekka Mecklin; Maartje Nielsen; Pål Møller
Journal:  Genet Med       Date:  2019-07-24       Impact factor: 8.822

10.  Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report.

Authors:  Toni T Seppälä; Aysel Ahadova; Mev Dominguez-Valentin; Finlay Macrae; D Gareth Evans; Christina Therkildsen; Julian Sampson; Rodney Scott; John Burn; Gabriela Möslein; Inge Bernstein; Elke Holinski-Feder; Kirsi Pylvänäinen; Laura Renkonen-Sinisalo; Anna Lepistö; Charlotte Kvist Lautrup; Annika Lindblom; John-Paul Plazzer; Ingrid Winship; Douglas Tjandra; Lior H Katz; Stefan Aretz; Robert Hüneburg; Stefanie Holzapfel; Karl Heinimann; Adriana Della Valle; Florencia Neffa; Nathan Gluck; Wouter H de Vos Tot Nederveen Cappel; Hans Vasen; Monika Morak; Verena Steinke-Lange; Christoph Engel; Nils Rahner; Wolff Schmiegel; Deepak Vangala; Huw Thomas; Kate Green; Fiona Lalloo; Emma J Crosbie; James Hill; Gabriel Capella; Marta Pineda; Matilde Navarro; Ignacio Blanco; Sanne Ten Broeke; Maartje Nielsen; Ken Ljungmann; Sigve Nakken; Noralane Lindor; Ian Frayling; Eivind Hovig; Lone Sunde; Matthias Kloor; Jukka-Pekka Mecklin; Mette Kalager; Pål Møller
Journal:  Hered Cancer Clin Pract       Date:  2019-02-28       Impact factor: 2.857

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1.  Systematic review: non-endoscopic surveillance for colorectal neoplasia in individuals with Lynch syndrome.

Authors:  Elsa L S A van Liere; Nanne K H de Boer; Evelien Dekker; Monique E van Leerdam; Tim G J de Meij; Dewkoemar Ramsoekh
Journal:  Aliment Pharmacol Ther       Date:  2022-02-18       Impact factor: 9.524

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