Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome
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Published:2020-06-12
Issue:10
Volume:28
Page:1387-1393
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ISSN:1018-4813
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Container-title:European Journal of Human Genetics
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language:en
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Short-container-title:Eur J Hum Genet
Author:
Tischkowitz MarcORCID, Colas Chrystelle, Pouwels Sjaak, Hoogerbrugge Nicoline, Bisseling Tanya, Bubien Virginie, Caux Frederic, Chabbert-Buffet Nathalie, Colas Chrystelle, Da Mota Gomes Sophie, Gotthardt Martin, Hoogerbrugge Nicoline, Kets Marleen, Lachlan Katherine L., Links Thera P., Longy Michel, Mann Ritse, Pouwels Sjaak, Kool Leo Schultze, Semple Robert K., Stock Ian, Tischkowitz Marc, Vos Janet, Hoogerbrugge Nicoline, Ligtenberg Marjolijn, Oostenbrink Rianne, Sijmons Rolf, Evans Gareth, Woodward Emma, Tischkowitz Marc, Maher Eamonn, Ferner Rosalie E., Aretz Stefan, Spier Isabel, Steinke-Lange Verena, Holinski-Feder Elke, Schröck Evelin, Frebourg Thierry, Houdayer Claude, Colas Chrystelle, Wolkenstein Pierre, Bours Vincent, Legius Eric, Poppe Bruce, Claes Kathleen, de Putter Robin, Guillermo Ignacio Blanco, Capella Gabriel, Vidal Joan Brunet, Lázaro Conxi, Balmaña Judith, Hernandez Hector Salvador, Oliveira Carla, Teixeira Manuel, Bajalica-Lagercrantz Svetlana, Tham Emma, Lubinski Jan, Ertmanska Karolina, Melegh Bela, Krajc Mateja, Blatnik Ana, Peltonen Sirkku, Hietala Marja, ,
Abstract
AbstractPTEN hamartoma tumour syndrome is a diverse multi-system disorder predisposing to the development of hamartomatous growths, increasing risk of breast, thyroid, renal cancer, and possibly increasing risk of endometrial cancer, colorectal cancer and melanoma. There is no international consensus on cancer surveillance in PHTS and all current guidelines are based on expert opinion. A comprehensive literature review was undertaken and guidelines were developed by clinicians with expertise from clinical genetics, gynaecology, endocrinology, dermatology, radiology, gastroenterology and general surgery, together with affected individuals and their representatives. Recommendations were put forward for surveillance for breast, thyroid and renal cancers. Limited recommendations were developed for other sites including endometrial, colon and skin. The proposed cancer surveillance recommendations for PHTS require a coordinated multidisciplinary approach and significant patient commitment. The evidence base for cancer surveillance in this guideline are limited, emphasising the need for prospective evaluation of the effectiveness of surveillance in the PHTS population.
Funder
Cancer Research UK
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference17 articles.
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