Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome

dc.contributor.authorTischkowitz Marc
dc.contributor.authorColas Chrystelle
dc.contributor.authorPouwels Sjak
dc.contributor.authorHoogerbrugge Nicoline
dc.contributor.authorPHTS Guideline Development Group & The European Reference Network GENTURIS
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organization-code1.2.246.10.2458963.20.39855016430
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.converis.publication-id51894875
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/51894875
dc.date.accessioned2022-10-28T13:49:57Z
dc.date.available2022-10-28T13:49:57Z
dc.description.abstract<i>PTEN </i>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.
dc.format.pagerange1393
dc.identifier.eissn1476-5438
dc.identifier.jour-issn1018-4813
dc.identifier.olddbid184613
dc.identifier.oldhandle10024/167707
dc.identifier.urihttps://www.utupub.fi/handle/11111/38663
dc.identifier.urnURN:NBN:fi-fe2021042823765
dc.language.isoen
dc.okm.affiliatedauthorPeltonen, Sirkku
dc.okm.affiliatedauthorHietala, Marja
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherNATURE PUBLISHING GROUP
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1038/s41431-020-0651-7
dc.relation.ispartofjournalEuropean Journal of Human Genetics
dc.relation.issue10
dc.relation.volume28
dc.source.identifierhttps://www.utupub.fi/handle/10024/167707
dc.titleCancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome
dc.year.issued2020

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