A. Swerdlow, Rosie Cooke, D. Beckers, B. Borgström, G. Butler, J. Carel, S. Cianfarani, P. Clayton, J. Coste, A. Deodati, E. Ecosse, R. Gausche, C. Giacomozzi, A. Hokken-Koelega, Aysha J. Khan, W. Kiess, C. Kuehni, P. Mullis, R. Pfaffle, L. Sävendahl, G. Sommer, Muriel Thomas, Anders Tidblad, S. Tollerfield, L. van Eycken, G. Zandwijken
{"title":"Cancer Risks in Patients Treated With Growth Hormone in Childhood: The SAGhE European Cohort Study","authors":"A. Swerdlow, Rosie Cooke, D. Beckers, B. Borgström, G. Butler, J. Carel, S. Cianfarani, P. Clayton, J. Coste, A. Deodati, E. Ecosse, R. Gausche, C. Giacomozzi, A. Hokken-Koelega, Aysha J. Khan, W. Kiess, C. Kuehni, P. Mullis, R. Pfaffle, L. Sävendahl, G. Sommer, Muriel Thomas, Anders Tidblad, S. Tollerfield, L. van Eycken, G. Zandwijken","doi":"10.1210/jc.2016-2046","DOIUrl":null,"url":null,"abstract":"Context\nGrowth 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.\n\n\nObjective\nTo examine cancer risks in relation to GH treatment.\n\n\nDesign\nCohort study.\n\n\nSetting\nPopulation-based.\n\n\nPatients\nCohort 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.\n\n\nMain Outcome Measures\nCancer incidence and cancer mortality.\n\n\nResults\nIncidence 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).\n\n\nConclusions\nOur 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.","PeriodicalId":22632,"journal":{"name":"The Journal of Clinical Endocrinology & Metabolism","volume":"19 1","pages":"1661–1672"},"PeriodicalIF":0.0000,"publicationDate":"2017-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"112","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Clinical Endocrinology & Metabolism","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1210/jc.2016-2046","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 112
Abstract
Context
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.