Literature DB >> 18061181

Validation and extension of the PREMM1,2 model in a population-based cohort of colorectal cancer patients.

Francesc Balaguer1, Judith Balmaña, Sergi Castellví-Bel, Ewout W Steyerberg, Montserrat Andreu, Xavier Llor, Rodrigo Jover, Sapna Syngal, Antoni Castells.   

Abstract

BACKGROUND & AIMS: Early recognition of patients at risk for Lynch syndrome is critical but often difficult. Recently, a predictive algorithm-the PREMM(1,2) model-has been developed to quantify the risk of carrying a germline mutation in the mismatch repair (MMR) genes MLH1 and MSH2. However, the model's performance in an unselected, population-based colorectal cancer population as well as its performance in combination with tumor MMR testing are unknown.
METHODS: We included all colorectal cancer cases from the EPICOLON study, a prospective, multicenter, population-based cohort (n = 1222). All patients underwent tumor microsatellite instability analysis and immunostaining for MLH1 and MSH2, and those with MMR deficiency (n = 91) underwent tumor BRAF V600E mutation analysis and MLH1/MSH2 germline testing.
RESULTS: The PREMM(1,2) model with a >/=5% cut-off had a sensitivity, specificity, and positive predictive value (PPV) of 100%, 68%, and 2%, respectively. The use of a higher PREMM(1,2) cut-off provided a higher specificity and PPV, at expense of a lower sensitivity. The combination of a >/=5% cut-off with tumor MMR testing maintained 100% sensitivity with an increased specificity (97%) and PPV (21%). The PPV of a PREMM(1,2) score >/=20% alone (16%) approached the PPV obtained with PREMM(1,2) score >/=5% combined with tumor MMR testing. In addition, a PREMM(1,2) score of <5% was associated with a high likelihood of a BRAF V600E mutation.
CONCLUSIONS: The PREMM(1,2) model is useful to identify MLH1/MSH2 mutation carriers among unselected colorectal cancer patients. Quantitative assessment of the genetic risk might be useful to decide on subsequent tumor MMR and germline testing.

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Year:  2007        PMID: 18061181      PMCID: PMC2542581          DOI: 10.1053/j.gastro.2007.10.042

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  27 in total

Review 1.  AGA technical review on hereditary colorectal cancer and genetic testing.

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4.  Immunohistochemistry for MSH2 and MHL1: a method for identifying mismatch repair deficient colorectal cancer.

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6.  Performance of different microsatellite marker panels for detection of mismatch repair-deficient colorectal tumors.

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9.  Frequency of hereditary non-polyposis colorectal cancer and other colorectal cancer familial forms in Spain: a multicentre, prospective, nationwide study.

Authors:  Virgínia Piñol; Montserrat Andreu; Antoni Castells; Artemio Payá; Xavier Bessa; Jover Rodrigo
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10.  Identification of MYH mutation carriers in colorectal cancer: a multicenter, case-control, population-based study.

Authors:  Francesc Balaguer; Sergi Castellví-Bel; Antoni Castells; Montserrat Andreu; Jenifer Muñoz; Javier P Gisbert; Xavier Llor; Rodrigo Jover; Rafael de Cid; Victòria Gonzalo; Xavier Bessa; Rosa M Xicola; Elisenda Pons; Cristina Alenda; Artemio Payá; Josep M Piqué
Journal:  Clin Gastroenterol Hepatol       Date:  2007-03       Impact factor: 11.382

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  21 in total

Review 1.  Lynch syndrome diagnostics: decision-making process for germ-line testing.

Authors:  E Lastra; M García-González; B Llorente; C Bernuy; M J Barrio; L Pérez-Cabornero; M Durán; C García-Girón
Journal:  Clin Transl Oncol       Date:  2012-04       Impact factor: 3.405

2.  The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history.

Authors:  Fay Kastrinos; Ewout W Steyerberg; Rowena Mercado; Judith Balmaña; Spring Holter; Steven Gallinger; Kimberly D Siegmund; James M Church; Mark A Jenkins; Noralane M Lindor; Stephen N Thibodeau; Lynn Anne Burbidge; Richard J Wenstrup; Sapna Syngal
Journal:  Gastroenterology       Date:  2010-08-19       Impact factor: 22.682

Review 3.  Clinical management of hereditary colorectal cancer syndromes.

Authors:  Hans F A Vasen; Ian Tomlinson; Antoni Castells
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2015-01-13       Impact factor: 46.802

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

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5.  Genetic counseling and cascade genetic testing in Lynch syndrome.

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Authors:  Wael M Abdel-Rahman
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7.  Identification of Lynch syndrome among patients with colorectal cancer.

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Journal:  JAMA       Date:  2012-10-17       Impact factor: 56.272

8.  Development and validation of a colon cancer risk assessment tool for patients undergoing colonoscopy.

Authors:  Fay Kastrinos; John I Allen; David H Stockwell; Elena M Stoffel; Earl F Cook; Muthoka L Mutinga; Judith Balmaña; Sapna Syngal
Journal:  Am J Gastroenterol       Date:  2009-04-28       Impact factor: 10.864

9.  Risk assessment, genetic testing, and management of Lynch syndrome.

Authors:  Shilpa Grover; Sapna Syngal
Journal:  J Natl Compr Canc Netw       Date:  2010-01       Impact factor: 11.908

10.  Aberrant gene promoter methylation associated with sporadic multiple colorectal cancer.

Authors:  Victoria Gonzalo; Juan José Lozano; Jenifer Muñoz; Francesc Balaguer; Maria Pellisé; Cristina Rodríguez de Miguel; Montserrat Andreu; Rodrigo Jover; Xavier Llor; M Dolores Giráldez; Teresa Ocaña; Anna Serradesanferm; Virginia Alonso-Espinaco; Mireya Jimeno; Miriam Cuatrecasas; Oriol Sendino; Sergi Castellví-Bel; Antoni Castells
Journal:  PLoS One       Date:  2010-01-19       Impact factor: 3.240

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