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Growth Hormone Deficiency and Treatment in Childhood Cancer Survivors

Growth hormone (GH) deficiency is a common pituitary hormone deficiency in childhood cancer survivors (CCS). The identification, diagnosis, and treatment of those individuals at risk are important in order to minimize associated morbidities that can be ameliorated by treatment with recombinant human...

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Autores principales: Pollock, Netanya I., Cohen, Laurie E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8569790/
https://www.ncbi.nlm.nih.gov/pubmed/34745010
http://dx.doi.org/10.3389/fendo.2021.745932
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author Pollock, Netanya I.
Cohen, Laurie E.
author_facet Pollock, Netanya I.
Cohen, Laurie E.
author_sort Pollock, Netanya I.
collection PubMed
description Growth hormone (GH) deficiency is a common pituitary hormone deficiency in childhood cancer survivors (CCS). The identification, diagnosis, and treatment of those individuals at risk are important in order to minimize associated morbidities that can be ameliorated by treatment with recombinant human GH therapy. However, GH and insulin-like growth factor-I have been implicated in tumorigenesis, so there has been concern over the use of GH therapy in patients with a history of malignancy. Reassuringly, GH therapy has not been shown to increase risk of tumor recurrence. These patients have an increased risk for development of meningiomas, but this may be related to their history of cranial irradiation rather than to GH therapy. In this review, we detail the CCS who are at risk for GHD and the existing evidence on the safety profile of GH therapy in this patient population.
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spelling pubmed-85697902021-11-06 Growth Hormone Deficiency and Treatment in Childhood Cancer Survivors Pollock, Netanya I. Cohen, Laurie E. Front Endocrinol (Lausanne) Endocrinology Growth hormone (GH) deficiency is a common pituitary hormone deficiency in childhood cancer survivors (CCS). The identification, diagnosis, and treatment of those individuals at risk are important in order to minimize associated morbidities that can be ameliorated by treatment with recombinant human GH therapy. However, GH and insulin-like growth factor-I have been implicated in tumorigenesis, so there has been concern over the use of GH therapy in patients with a history of malignancy. Reassuringly, GH therapy has not been shown to increase risk of tumor recurrence. These patients have an increased risk for development of meningiomas, but this may be related to their history of cranial irradiation rather than to GH therapy. In this review, we detail the CCS who are at risk for GHD and the existing evidence on the safety profile of GH therapy in this patient population. Frontiers Media S.A. 2021-10-22 /pmc/articles/PMC8569790/ /pubmed/34745010 http://dx.doi.org/10.3389/fendo.2021.745932 Text en Copyright © 2021 Pollock and Cohen https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Pollock, Netanya I.
Cohen, Laurie E.
Growth Hormone Deficiency and Treatment in Childhood Cancer Survivors
title Growth Hormone Deficiency and Treatment in Childhood Cancer Survivors
title_full Growth Hormone Deficiency and Treatment in Childhood Cancer Survivors
title_fullStr Growth Hormone Deficiency and Treatment in Childhood Cancer Survivors
title_full_unstemmed Growth Hormone Deficiency and Treatment in Childhood Cancer Survivors
title_short Growth Hormone Deficiency and Treatment in Childhood Cancer Survivors
title_sort growth hormone deficiency and treatment in childhood cancer survivors
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8569790/
https://www.ncbi.nlm.nih.gov/pubmed/34745010
http://dx.doi.org/10.3389/fendo.2021.745932
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