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dc.contributor.authorSwerdlow, AJ
dc.contributor.authorCooke, R
dc.contributor.authorBeckers, D
dc.contributor.authorBorgström, B
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.authorGausche, R
dc.contributor.authorGiacomozzi, C
dc.contributor.authorHokken-Koelega, ACS
dc.contributor.authorKhan, AJ
dc.contributor.authorKiess, W
dc.contributor.authorKuehni, CE
dc.contributor.authorMullis, P-E
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.authorVan Eycken, L
dc.contributor.authorZandwijken, GRJ
dc.date.accessioned2017-05-23T15:31:47Z
dc.date.issued2017-05-01
dc.identifier.citationThe Journal of clinical endocrinology and metabolism, 2017, 102 (5), pp. 1661 - 1672
dc.identifier.issn0021-972X
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/648
dc.identifier.eissn1945-7197
dc.identifier.doi10.1210/jc.2016-2046
dc.description.abstractCONTEXT: Growth hormone (GH) is prescribed for an increasing range of indications, but there has been concern that it might raise cancer risk. Published data are limited. OBJECTIVE: To examine cancer risks in relation to GH treatment. DESIGN: Cohort study. SETTING: Population-based. PATIENTS: Cohort of 23,984 patients treated with recombinant human GH (r-hGH) in eight European countries since this treatment was first used in 1984. Cancer expectations from country-specific national population statistics. MAIN OUTCOME MEASURES: Cancer incidence and cancer mortality. RESULTS: Incidence and mortality risks in the cohort were raised for several cancer sites, largely consequent on second primary malignancies in patients given r-hGH after cancer treatment. There was no clear raised risk in patients with growth failure without other major disease. Only for bone and bladder cancers was incidence significantly raised in GH-treated patients without previous cancer. Cancer risk was unrelated to duration or cumulative dose of r-hGH treatment, but for patients treated after previous cancer, cancer mortality risk increased significantly with increasing daily r-hGH dose (P trend < 0.001). Hodgkin lymphoma (HL) incidence increased significantly with longer follow-up (P trend = 0.001 for patients overall and 0.002 for patients without previous cancer). CONCLUSIONS: Our results do not generally support a carcinogenic effect of r-hGH, but the unexplained trend in cancer mortality risk in relation to GH dose in patients with previous cancer, and the indication of possible effects on bone cancer, bladder cancer, and HL risks, need further investigation.
dc.formatPrint
dc.format.extent1661 - 1672
dc.languageeng
dc.language.isoeng
dc.publisherENDOCRINE SOC
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectHumans
dc.subjectNeoplasms
dc.subjectHodgkin Disease
dc.subjectBone Neoplasms
dc.subjectNeoplasms, Second Primary
dc.subjectBone Diseases, Developmental
dc.subjectHypopituitarism
dc.subjectTurner Syndrome
dc.subjectGrowth Disorders
dc.subjectHuman Growth Hormone
dc.subjectRecombinant Proteins
dc.subjectIncidence
dc.subjectRisk
dc.subjectCohort Studies
dc.subjectDose-Response Relationship, Drug
dc.subjectAdolescent
dc.subjectChild
dc.subjectChild, Preschool
dc.subjectInfant
dc.subjectInfant, Newborn
dc.subjectEurope
dc.subjectFemale
dc.subjectMale
dc.subjectRenal Insufficiency, Chronic
dc.subjectUrinary Bladder Neoplasms
dc.subjectYoung Adult
dc.titleCancer Risks in Patients Treated With Growth Hormone in Childhood: The SAGhE European Cohort Study.
dc.typeJournal Article
dcterms.dateAccepted2017-01-26
rioxxterms.versionofrecord10.1210/jc.2016-2046
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2017-05
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfThe Journal of clinical endocrinology and metabolism
pubs.issue5
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.volume102
pubs.embargo.termsNot known
icr.researchteamAetiological Epidemiology
dc.contributor.icrauthorSwerdlow, Anthony


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