NCCN临床实践指南_遗传_家族高风险评估-结直肠癌(2019.V2)英文版
99页1、Version 2 2019 08 08 19 2019 National Comprehensive Cancer Network NCCN All rights reserved NCCN Guidelines and this illustration may not be reproduced in any form without the express written permission of NCCN NCCN Clinical Practice Guidelines in Oncology NCCN Guidelines Genetic Familial High Risk Assessment Colorectal Version 2 2019 August 8 2019 Continue NCCN org NCCN Guidelines Version 2 2019 Genetic Familial High Risk Assessment Colorectal Version 2 2019 08 08 19 2019 National Comprehensive
2、 Cancer Network NCCN All rights reserved NCCN Guidelines and this illustration may not be reproduced in any form without the express written permission of NCCN NCCN Guidelines Index Table of Contents Discussion NCCN Guidelines Panel Disclosures Continue Dawn Provenzale MD MS Chair Duke Cancer Institute Samir Gupta MD Vice chair UC San Diego Moores Cancer Center Dennis J Ahnen MD University of Colorado Cancer Center Lee May Chen MD UCSF Helen Diller Family Comprehensive Cancer Center Daniel C Chu
3、ng MD Massachusetts General Hospital Cancer Center Gregory Cooper MD Case Comprehensive Cancer Center University Hospitals Seidman Cancer Center and Cleveland Clinic Taussig Cancer Institute Dayna S Early MD Siteman Cancer Center at Barnes Jewish Hospital and Washington University School of Medicine Francis M Giardiello MD MBA The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins William Grady MD Fred Hutchinson Cancer Research Center Seattle Cancer Care Alliance Michael J Hall MD MS Fo
4、x Chase Cancer Center Amy L Halverson MD Robert H Lurie Comprehensive Cancer Center of Northwestern University Stanley R Hamilton MD The University of Texas MD Anderson Cancer Center Heather Hampel MS CGC The Ohio State University Comprehensive Cancer Center James Cancer Hospital and Solove Research Institute Sigurdis Haraldsdottir MD PhD Stanford Cancer Institute Priyanka Kanth MD MS Huntsman Cancer Institute at the University of Utah Jason B Klapman MD Moffitt Cancer Center Audrey J Lazenby MD
5、 Fred 110 1059 1066 Footnote c was added Irrespective of degree of relatedness Also for LS 1 and POLYP 1 HRS 2 Qualifier 5 serrated polyps was revised by adding proximal to sigmoid colon After qualifier 10 adenomas Rare genetic causes of multiple adenomatous polyps was added with corresponding footnote i HRS 3 The Criteria for the Evaluation of Lynch Syndrome were reorganized by personal history family history and increased model predicted risk for Lynch syndrome Personal history 3rd sub bullet
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