Literature DB >> 31981079

SEOM clinical guideline on hereditary colorectal cancer (2019).

C Guillén-Ponce1, E Lastra2, I Lorenzo-Lorenzo3, T Martín Gómez4, R Morales Chamorro5, A B Sánchez-Heras6, R Serrano7, M C Soriano Rodríguez8, J L Soto9, L Robles10.   

Abstract

In the last 2 decades, clinical genetics on hereditary colorectal syndromes has shifted from just a molecular characterization of the different syndromes to the estimation of the individual risk of cancer and appropriate risk reduction strategies. In the last years, new specific therapies for some subgroups of patients have emerged as very effective alternatives. At the same time, germline multigene panel testing by next-generation sequencing (NGS) technology has become the new gold standard for molecular genetics.

Entities:  

Keywords:  Adenomatous polyposis; Colon cancer; Hereditary colorectal cancer; Lynch syndrome

Year:  2020        PMID： 31981079     DOI： 10.1007/s12094-019-02272-y

Source DB:  PubMed          Journal:  Clin Transl Oncol        ISSN： 1699-048X            Impact factor:   3.405


  46 in total

1.  Endoscopic management of polyposis syndromes: European Society of Gastrointestinal Endoscopy (ESGE) Guideline.

Authors:  Monique E van Leerdam; Victorine H Roos; Jeanin E van Hooft; Evelien Dekker; Rodrigo Jover; Michal F Kaminski; Andrew Latchford; Helmut Neumann; Maria Pellisé; Jean-Christophe Saurin; Pieter J Tanis; Anja Wagner; Francesc Balaguer; Luigi Ricciardiello
Journal:  Endoscopy       Date:  2019-07-23       Impact factor: 10.093

2.  The American Society of Colon and Rectal Surgeons Clinical Practice Guidelines for the Management of Inherited Polyposis Syndromes.

Authors:  Daniel Herzig; Karin Hardiman; Martin Weiser; Nancy You; Ian Paquette; Daniel L Feingold; Scott R Steele
Journal:  Dis Colon Rectum       Date:  2017-09       Impact factor: 4.585

3.  The history of Lynch syndrome.

Authors:  C Richard Boland; Henry T Lynch
Journal:  Fam Cancer       Date:  2013-06       Impact factor: 2.375

4.  Assessment of Tumor Sequencing as a Replacement for Lynch Syndrome Screening and Current Molecular Tests for Patients With Colorectal Cancer.

Authors:  Heather Hampel; Rachel Pearlman; Mallory Beightol; Weiqiang Zhao; Daniel Jones; Wendy L Frankel; Paul J Goodfellow; Ahmet Yilmaz; Kristin Miller; Jason Bacher; Angela Jacobson; Electra Paskett; Peter G Shields; Richard M Goldberg; Albert de la Chapelle; Brian H Shirts; Colin C Pritchard
Journal:  JAMA Oncol       Date:  2018-06-01       Impact factor: 31.777

5.  Development and Validation of the PREMM5 Model for Comprehensive Risk Assessment of Lynch Syndrome.

Authors:  Fay Kastrinos; Hajime Uno; Chinedu Ukaegbu; Carmelita Alvero; Ashley McFarland; Matthew B Yurgelun; Matthew H Kulke; Deborah Schrag; Jeffrey A Meyerhardt; Charles S Fuchs; Robert J Mayer; Kimmie Ng; Ewout W Steyerberg; Sapna Syngal
Journal:  J Clin Oncol       Date:  2017-05-10       Impact factor: 44.544

6.  Prevalence of Germline Mutations in Polyposis and Colorectal Cancer-Associated Genes in Patients With Multiple Colorectal Polyps.

Authors:  Peter P Stanich; Rachel Pearlman; Alice Hinton; Stephanie Gutierrez; Holly LaDuca; Heather Hampel; Kory Jasperson
Journal:  Clin Gastroenterol Hepatol       Date:  2018-12-14       Impact factor: 11.382

7.  Universal Screening for Mismatch-Repair Deficiency in Endometrial Cancers to Identify Patients With Lynch Syndrome and Lynch-like Syndrome.

Authors:  Jaclyn C Watkins; Eric J Yang; Michael G Muto; Colleen M Feltmate; Ross S Berkowitz; Neil S Horowitz; Sapna Syngal; Matthew B Yurgelun; Anu Chittenden; Jason L Hornick; Christopher P Crum; Lynette M Sholl; Brooke E Howitt
Journal:  Int J Gynecol Pathol       Date:  2017-03       Impact factor: 2.762

8.  Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing.

Authors:  Daniel D Buchanan; Yen Y Tan; Michael D Walsh; Mark Clendenning; Alexander M Metcalf; Kaltin Ferguson; Sven T Arnold; Bryony A Thompson; Felicity A Lose; Michael T Parsons; Rhiannon J Walters; Sally-Ann Pearson; Margaret Cummings; Martin K Oehler; Penelope B Blomfield; Michael A Quinn; Judy A Kirk; Colin J Stewart; Andreas Obermair; Joanne P Young; Penelope M Webb; Amanda B Spurdle
Journal:  J Clin Oncol       Date:  2013-12-09       Impact factor: 44.544

9.  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

Review 10.  PTEN Hamartoma Tumor Syndrome: A Clinical Overview.

Authors:  Robert Pilarski
Journal:  Cancers (Basel)       Date:  2019-06-18       Impact factor: 6.639
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  3 in total

1.  2019 SEOM guidelines (the end of a decade).

Authors:  A González-Del-Alba; Á Rodríguez-Lescure
Journal:  Clin Transl Oncol       Date:  2020-02-06       Impact factor: 3.405

2.  Reporting quality of practice guidelines on colorectal cancer: evaluation using the RIGHT reporting checklist.

Authors:  Jing Han; Meng Tao; Xuan Wu; Ding Li; Yanfang Ma; Shaheenah Dawood; Colin W Steele; Ker-Kan Tan; Qiming Wang
Journal:  Ann Transl Med       Date:  2021-07

3.  Increased Co-Occurrence of Pathogenic Variants in Hereditary Breast and Ovarian Cancer and Lynch Syndromes: A Consequence of Multigene Panel Genetic Testing?

Authors:  Mar Infante; Mónica Arranz-Ledo; Enrique Lastra; Luis Enrique Abella; Raquel Ferreira; Marta Orozco; Lara Hernández; Noemí Martínez; Mercedes Durán
Journal:  Int J Mol Sci       Date:  2022-09-29       Impact factor: 6.208
  3 in total

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