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GH safety workshop position paper: a critical appraisal of recombinant human GH therapy in children and adults

Date
2016
Author
Cohen, P.
Boguszewski, M.
Burman, P.
Butler, G.
Chihara, K.
Christiansen, J.
Clayton, P.
Clemmons, D.
Deal, C.
Dunger, D.
Erfurth, E. M.
Fuqua, J. S.
Grimberg, A.
Haymond, M.
Higham, C.
Ho, K.
Hoffman, A. R.
Hokken-Koelega, A.
Johannsson, G.
Juul, A.
Kopchick, J.
Lee, P.
Pollak, M.
Radovick, S.
Robison, L.
Rosenfeld, R.
Ross, R. J.
Savendahl, L.
Saenger, P.
Sorensen, H. Toft
Stochholm, K.
Strasburger, C.
Swerdlow, A.
Thorner, M.
Darendeliler, Fatma Feyza
Cianfarani, S.
Allen, D. B.
Backeljauw, P.
Bidlingmaier, M.
Biller, B. M. K.
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Abstract
Recombinant human GH (rhGH) has been in use for 30 years, and over that time its safety and efficacy in children and adults has been subject to considerable scrutiny. In 2001, a statement from the GH Research Society (GRS) concluded that 'for approved indications, GH is safe'; however, the statement highlighted a number of areas for on-going surveillance of long-term safety, including cancer risk, impact on glucose homeostasis, and use of high dose pharmacological rhGH treatment. Over the intervening years, there have been a number of publications addressing the safety of rhGH with regard to mortality, cancer and cardiovascular risk, and the need for long-term surveillance of the increasing number of adults who were treated with rhGH in childhood. Against this backdrop of interest in safety, the European Society of Paediatric Endocrinology (ESPE), the GRS, and the Pediatric Endocrine Society (PES) convened a meeting to reappraise the safety of rhGH. The ouput of the meeting is a concise position statement.
URI
http://hdl.handle.net/20.500.12627/12695
https://doi.org/10.1530/eje-15-0873
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Creative Commons Lisansı

İstanbul Üniversitesi Akademik Arşiv Sistemi (ilgili içerikte aksi belirtilmediği sürece) Creative Commons Alıntı-GayriTicari-Türetilemez 4.0 Uluslararası Lisansı ile lisanslanmıştır.

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