Literature DB >> 36251064

Risk of cancer in individuals with Lynch-like syndrome and their families: a systematic review.

Pandu P Nugroho1,2, Siti Alyaa S Ghozali1,2, Daniel D Buchanan3,4,5, Mia I Pisano6, Jeanette C Reece7.   

Abstract

BACKGROUND: Lynch-like syndrome (LLS) tumors have similar clinicopathological features to Lynch syndrome (LS) tumors but have no identifiable pathogenic germline mismatch repair gene variant. However, cancer risks in LLS patients and first-degree relatives (FDRs) are not well defined.
METHODS: To clarify LLS-associated cancer risks, a systematic review of all studies examining all cancer risks in LLS was performed. Searching of Medline, Embase, Pubmed, Cochrane and CINAHL databases and reference/citation checking identified relevant studies published between January 1, 1980 and February 11, 2021. Joanna Briggs Institute Appraisal Tools assessed the risk of bias.
RESULTS: Six studies (five cohort/one cross-sectional) were eligible for study inclusion. One study found no difference in colorectal cancer (CRC) incidence between LLS and LS patients or CRC risks at aged 70 years. Three studies found CRC incidence in LLS FDRs was higher than the general population but lower than LS FDRs. Two studies showed no difference in CRC diagnosis age between LLS patients and LS patients. Endometrial cancer risks in LLS patients were higher than the general population but lower than LS patients.
CONCLUSION: Evidence of elevated CRC risks in LLS patients and FDRs supports increased colonoscopy surveillance strategies for LLS patients and FDRs in line with current recommendations for LS. Due to heterogeneity amongst LLS populations, extended intervals between screening may be advised for low-risk families. Studies to resolve the molecular characterization and definition of LLS are needed to clarify cancer risks associated with LLS which in turn may individualize surveillance strategies for LLS patients and families.
© 2022. The Author(s).

Entities:  

Keywords:  Colorectal cancer; Extra-colonic cancer; Lynch syndrome; Lynch-like syndrome; Standard incidence ratio

Year:  2022        PMID: 36251064     DOI: 10.1007/s00432-022-04397-0

Source DB:  PubMed          Journal:  J Cancer Res Clin Oncol        ISSN: 0171-5216            Impact factor:   4.322


  39 in total

1.  Decision support tools to improve cancer diagnostic decision making in primary care: a systematic review.

Authors:  Sophie Chima; Jeanette C Reece; Kristi Milley; Shakira Milton; Jennifer G McIntosh; Jon D Emery
Journal:  Br J Gen Pract       Date:  2019-11-28       Impact factor: 5.386

2.  Mutation deep within an intron of MSH2 causes Lynch syndrome.

Authors:  Mark Clendenning; Daniel D Buchanan; Michael D Walsh; Belinda Nagler; Christophe Rosty; Bryony Thompson; Amanda B Spurdle; John L Hopper; Mark A Jenkins; Joanne P Young
Journal:  Fam Cancer       Date:  2011-06       Impact factor: 2.375

3.  Prevalence of Lynch syndrome and Lynch-like syndrome among patients with colorectal cancer in a Japanese hospital-based population.

Authors:  Noriyasu Chika; Hidetaka Eguchi; Kensuke Kumamoto; Okihide Suzuki; Keiichiro Ishibashi; Tetsuhiko Tachikawa; Kiwamu Akagi; Jun-Ichi Tamaru; Yasushi Okazaki; Hideyuki Ishida
Journal:  Jpn J Clin Oncol       Date:  2017-02-09       Impact factor: 3.019

4.  Hereditary non-polyposis colorectal cancer: current risks of colorectal cancer largely overestimated.

Authors:  J Carayol; M Khlat; J Maccario; C Bonaïti-Pellié
Journal:  J Med Genet       Date:  2002-05       Impact factor: 6.318

5.  Differentiating Lynch-like from Lynch syndrome.

Authors:  John M Carethers
Journal:  Gastroenterology       Date:  2014-01-24       Impact factor: 22.682

Review 6.  Lynch syndrome and Lynch syndrome mimics: The growing complex landscape of hereditary colon cancer.

Authors:  John M Carethers; Elena M Stoffel
Journal:  World J Gastroenterol       Date:  2015-08-21       Impact factor: 5.742

7.  Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.

Authors:  Freddie Bray; Jacques Ferlay; Isabelle Soerjomataram; Rebecca L Siegel; Lindsey A Torre; Ahmedin Jemal
Journal:  CA Cancer J Clin       Date:  2018-09-12       Impact factor: 508.702

Review 8.  Clinical problems of colorectal cancer and endometrial cancer cases with unknown cause of tumor mismatch repair deficiency (suspected Lynch syndrome).

Authors:  Daniel D Buchanan; Christophe Rosty; Mark Clendenning; Amanda B Spurdle; Aung Ko Win
Journal:  Appl Clin Genet       Date:  2014-10-06

9.  Cancer risks in Lynch syndrome, Lynch-like syndrome, and familial colorectal cancer type X: a prospective cohort study.

Authors:  Karolin Bucksch; Silke Zachariae; Stefan Aretz; Reinhard Büttner; Elke Holinski-Feder; Stefanie Holzapfel; Robert Hüneburg; Matthias Kloor; Magnus von Knebel Doeberitz; Monika Morak; Gabriela Möslein; Jacob Nattermann; Claudia Perne; Nils Rahner; Wolff Schmiegel; Karsten Schulmann; Verena Steinke-Lange; Christian P Strassburg; Deepak B Vangala; Jürgen Weitz; Markus Loeffler; Christoph Engel
Journal:  BMC Cancer       Date:  2020-05-24       Impact factor: 4.430

10.  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

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