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dc.contributor.authorSwerdlow, AJ
dc.contributor.authorCooke, R
dc.contributor.authorBeckers, D
dc.contributor.authorButler, G
dc.contributor.authorCarel, J-C
dc.contributor.authorCianfarani, S
dc.contributor.authorClayton, P
dc.contributor.authorCoste, J
dc.contributor.authorDeodati, A
dc.contributor.authorEcosse, E
dc.contributor.authorHokken-Koelega, ACS
dc.contributor.authorKhan, AJ
dc.contributor.authorKiess, W
dc.contributor.authorKuehni, CE
dc.contributor.authorFlück, CE
dc.contributor.authorPfaffle, R
dc.contributor.authorSävendahl, L
dc.contributor.authorSommer, G
dc.contributor.authorThomas, M
dc.contributor.authorTidblad, A
dc.contributor.authorTollerfield, S
dc.contributor.authorZandwijken, GRJ
dc.date.accessioned2018-08-16T10:33:20Z
dc.date.issued2019-03-01
dc.identifier.citationThe Journal of clinical endocrinology and metabolism, 2019, 104 (3), pp. 658 - 664
dc.identifier.issn0021-972X
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/2339
dc.identifier.eissn1945-7197
dc.identifier.doi10.1210/jc.2018-01133
dc.description.abstractCONTEXT: There has been concern that GH treatment of children might increase meningioma risk. Results of published studies have been inconsistent and limited. OBJECTIVE: To examine meningioma risks in relation to GH treatment. DESIGN: Cohort study with follow-up via cancer registries and other registers. SETTING: Population-based. PATIENTS: A cohort of 10,403 patients treated in childhood with recombinant GH in five European countries since this treatment was first used in 1984. Expected rates from national cancer registration statistics. MAIN OUTCOME MEASURES: Risk of meningioma incidence. RESULTS: During follow-up, 38 meningiomas occurred. Meningioma risk was greatly raised in the cohort overall [standardized incidence ratio (SIR) = 75.4; 95% CI: 54.9 to 103.6], as a consequence of high risk in subjects who had received radiotherapy for underlying malignancy (SIR = 658.4; 95% CI: 460.4 to 941.7). Risk was not significantly raised in patients who did not receive radiotherapy. Risk in radiotherapy-treated patients was not significantly related to mean daily dose of GH, duration of GH treatment, or cumulative dose of GH. CONCLUSIONS: Our data add to evidence of very high risk of meningioma in patients treated in childhood with GH after cranial radiotherapy, but suggest that GH may not affect radiotherapy-related risk, and that there is no material raised risk of meningioma in GH-treated patients who did not receive radiotherapy.
dc.formatPrint
dc.format.extent658 - 664
dc.languageeng
dc.language.isoeng
dc.publisherENDOCRINE SOC
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectHumans
dc.subjectMeningioma
dc.subjectMeningeal Neoplasms
dc.subjectNeoplasms, Second Primary
dc.subjectGrowth Disorders
dc.subjectHuman Growth Hormone
dc.subjectRecombinant Proteins
dc.subjectCranial Irradiation
dc.subjectRegistries
dc.subjectIncidence
dc.subjectRisk Assessment
dc.subjectFollow-Up Studies
dc.subjectAdolescent
dc.subjectAdult
dc.subjectChild
dc.subjectChild, Preschool
dc.subjectInfant
dc.subjectInfant, Newborn
dc.subjectEurope
dc.subjectFemale
dc.subjectMale
dc.subjectYoung Adult
dc.titleRisk of Meningioma in European Patients Treated With Growth Hormone in Childhood: Results From the SAGhE Cohort.
dc.typeJournal Article
dcterms.dateAccepted2018-08-14
rioxxterms.versionofrecord10.1210/jc.2018-01133
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2019-03
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfThe Journal of clinical endocrinology and metabolism
pubs.issue3
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Aetiological Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Aetiological Epidemiology
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Aetiological Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Aetiological Epidemiology
pubs.publication-statusPublished
pubs.volume104
pubs.embargo.termsNot known
icr.researchteamAetiological Epidemiology
dc.contributor.icrauthorSwerdlow, Anthony


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