Raman Sripriya, Grimberg Adda, Waguespack Steven G, Miller Bradley S, Sklar Charles A, Meacham Lillian R, Patterson Briana C
Division of Pediatric Endocrinology (S.R.), Children's Mercy Hospital, University of Missouri, Kansas City, Missouri 64111; University of Kansas Medical Center (S.R.), Kansas City, Kansas 66160; Department of Pediatrics (A.G.), Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104; Division of Endocrinology and Diabetes (A.G.), The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104; Department of Endocrine Neoplasia and Hormonal Disorders (S.G.W.), University of Texas MD Anderson Cancer Center, Houston, Texas 77030; Division of Endocrinology (B.S.M.), Department of Pediatrics, University of Minnesota Masonic Children's Hospital, Minneapolis, Minnesota 55455; Memorial Sloan Kettering Cancer Center (C.A.S.), New York, New York 10065; and Emory University/Aflac Cancer and Blood Disorders Center of Children's Healthcare of Atlanta (L.R.M., B.C.P.), Atlanta, Georgia 30322.
J Clin Endocrinol Metab. 2015 Jun;100(6):2192-203. doi: 10.1210/jc.2015-1002. Epub 2015 Apr 3.
GH and IGF-1 have been shown to affect tumor growth in vitro and in some animal models. This report summarizes the available evidence on whether GH therapy in childhood is associated with an increased risk of neoplasia during treatment or after treatment is completed.
A PubMed search conducted through February 2014 retrieved original articles written in English addressing GH therapy and neoplasia risk. Subsequent searches were done to include additional relevant publications.
In children without prior cancer or known risk factors for developing cancer, the clinical evidence does not affirm an association between GH therapy during childhood and neoplasia. GH therapy has not been reported to increase the risk for neoplasia in this population, although most of these data are derived from postmarketing surveillance studies lacking rigorous controls. In patients who are at higher risk for developing cancer, current evidence is insufficient to conclude whether or not GH further increases cancer risk. GH treatment of pediatric cancer survivors does not appear to increase the risk of recurrence but may increase their risk for subsequent primary neoplasms.
In children without known risk factors for malignancy, GH therapy can be safely administered without concerns about an increased risk for neoplasia. GH use in children with medical diagnoses predisposing them to the development of malignancies should be critically analyzed on an individual basis, and if chosen, appropriate surveillance for malignancies should be undertaken. GH can be used to treat GH-deficient childhood cancer survivors who are in remission with the understanding that GH therapy may increase their risk for second neoplasms.
生长激素(GH)和胰岛素样生长因子-1(IGF-1)已被证明在体外及一些动物模型中会影响肿瘤生长。本报告总结了关于儿童期GH治疗是否与治疗期间或治疗结束后肿瘤形成风险增加相关的现有证据。
通过检索截至2014年2月的PubMed数据库,获取了以英文撰写的关于GH治疗与肿瘤形成风险的原始文章。随后进行了进一步检索以纳入其他相关出版物。
在无既往癌症或已知癌症发生风险因素的儿童中,临床证据并未证实儿童期GH治疗与肿瘤形成之间存在关联。尽管这些数据大多来自缺乏严格对照的上市后监测研究,但尚未有报道称GH治疗会增加该人群的肿瘤形成风险。对于癌症发生风险较高的患者,目前的证据不足以得出GH是否会进一步增加癌症风险的结论。对儿童癌症幸存者进行GH治疗似乎不会增加复发风险,但可能会增加其随后发生原发性肿瘤的风险。
在无已知恶性肿瘤风险因素的儿童中,可以安全地进行GH治疗,而无需担心肿瘤形成风险增加。对于因医学诊断而易患恶性肿瘤的儿童使用GH,应基于个体情况进行严格分析,若选择使用,则应进行适当的恶性肿瘤监测。GH可用于治疗处于缓解期的生长激素缺乏的儿童癌症幸存者,但应了解GH治疗可能会增加他们发生第二肿瘤的风险。