Context 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.

Swerdlow, A.j., Cooke, R., Beckers, D., Butler, G., Carel, J.-., Cianfarani, S., et al. (2019). Risk of Meningioma in European Patients Treated with Growth Hormone in Childhood: Results from the SAGhE Cohort. THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM, 104(3), 658-664 [10.1210/jc.2018-01133].

Risk of Meningioma in European Patients Treated with Growth Hormone in Childhood: Results from the SAGhE Cohort

Cianfarani S.;Deodati A.;
2019-01-01

Abstract

Context 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.
2019
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA
English
Adolescent; Adult; Child; Child, Preschool; Cranial Irradiation; Europe; Female; Follow-Up Studies; Growth Disorders; Human Growth Hormone; Humans; Incidence; Infant; Infant, Newborn; Male; Meningeal Neoplasms; Meningioma; Neoplasms, Second Primary; Recombinant Proteins; Registries; Risk Assessment; Young Adult
http://jcem.endojournals.org
Swerdlow, A.j., Cooke, R., Beckers, D., Butler, G., Carel, J.-., Cianfarani, S., et al. (2019). Risk of Meningioma in European Patients Treated with Growth Hormone in Childhood: Results from the SAGhE Cohort. THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM, 104(3), 658-664 [10.1210/jc.2018-01133].
Swerdlow, Aj; Cooke, R; Beckers, D; Butler, G; Carel, J-; Cianfarani, S; Clayton, P; Coste, J; Deodati, A; Ecosse, E; Hokken-Koelega, Acs; Khan, Aj; K...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/232152
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