Genetic/familial high-risk assessment: Colorectal, version 2.2019: Featured updates to the NCCN Guidelines Guidelines
| Authors: | Gupta, S.; Provenzale, D.; Llor, X.; Halverson, A. L.; Grady, W.; Chung, D. C.; Haraldsdottir, S.; Markowitz, A. J.; Slavin, T. P. Jr; Hampel, H.; Ness, R. M.; Weiss, J. M.; Ahnen, D. J.; Chen, L. M.; Cooper, G.; Early, D. S.; Giardiello, F. M.; Hall, M. J.; Hamilton, S. R.; Kanth, P.; Klapman, J. B.; Lazenby, A. J.; Lynch, P. M.; Mayer, R. J.; Mikkelson, J.; Peter, S.; Regenbogen, S. E.; Dwyer, M. A.; Ogba, N. |
| Title: | Genetic/familial high-risk assessment: Colorectal, version 2.2019: Featured updates to the NCCN Guidelines |
| Abstract: | Identifying individuals with hereditary syndromes allows for improved cancer surveillance, risk reduction, and optimized management. Establishing criteria for assessment allows for the identification of individuals who are carriers of pathogenic genetic variants. The NCCN Guidelines for Genetic/Familial High-Risk Assessment: Colorectal provide recommendations for the assessment and management of patients with high-risk colorectal cancer syndromes. These NCCN Guidelines Insights focus on criteria for the evaluation of Lynch syndrome and considerations for use of multigene testing in the assessment of hereditary colorectal cancer syndromes. © National Comprehensive Cancer Network, Inc. 2019. All rights reserved. |
| Journal Title: | Journal of the National Comprehensive Cancer Network |
| Volume: | 17 |
| Issue: | 9 |
| ISSN: | 1540-1405 |
| Publisher: | Harborside Press |
| Date Published: | 2019-09-01 |
| Start Page: | 1032 |
| End Page: | 1041 |
| Language: | English |
| DOI: | 10.6004/jnccn.2019.0044 |
| PUBMED: | 31487681 |
| PROVIDER: | scopus |
| DOI/URL: | |
| Notes: | Article -- Export Date: 1 October 2019 -- Source: Scopus |
