儿童时期接受生长激素治疗的患者的癌症风险:SAGhE欧洲队列研究

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
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引用次数: 112

摘要

生长激素(GH)被用于越来越多的适应症,但人们一直担心它可能会增加患癌症的风险。发表的数据有限。目的探讨生长激素治疗与肿瘤风险的关系。DesignCohort study.SettingPopulation-based。自1984年首次使用重组人生长激素(r-hGH)治疗以来,8个欧洲国家的23,984例患者的患者记录。根据具体国家人口统计得出的癌症预期。主要结局指标:癌症发病率和癌症死亡率。结果该队列中几个癌症部位的发病率和死亡率风险升高,主要是由于癌症治疗后给予r-hGH的患者出现第二原发恶性肿瘤。在没有其他主要疾病的生长衰竭患者中没有明显的风险增加。只有骨癌和膀胱癌的发病率在没有既往癌症的gh治疗患者中显著升高。癌症风险与r-hGH治疗的持续时间或累积剂量无关,但对于既往癌症后接受治疗的患者,癌症死亡风险随着r-hGH每日剂量的增加而显著增加(P趋势< 0.001)。霍奇金淋巴瘤(HL)的发病率随着随访时间的延长而显著增加(总体患者P趋势= 0.001,既往无癌症患者P趋势= 0.002)。结论我们的研究结果并不普遍支持r-hGH的致癌作用,但在既往癌症患者中,肿瘤死亡风险与GH剂量之间的不明趋势,以及对骨癌、膀胱癌和HL风险的可能影响,需要进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cancer Risks in Patients Treated With Growth Hormone in Childhood: The SAGhE European Cohort Study
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.
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