Marcianò Ilaria, Ingrasciotta Ylenia, Giorgianni Francesco, Ientile Valentina, Chinellato Alessandro, Tari Daniele Ugo, Gini Rosa, Cannavò Salvatore, Pastorello Maurizio, Scondotto Salvatore, Cananzi Pasquale, Traversa Giuseppe, Trotta Francesco, Belleudi Valeria, Addis Antonio, Trifirò Gianluca
Unit of Clinical Pharmacology, A.O.U. Policlinico "G. Martino", Messina, Italy.
Department of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina, Messina, Italy.
Front Endocrinol (Lausanne). 2018 Mar 13;9:95. doi: 10.3389/fendo.2018.00095. eCollection 2018.
Somatropin [recombinant growth hormone (rGH)] is approved in children and adults for several conditions involving growth disturbances and the corresponding biosimilar is available in Italy since 2006. No population-based data are available on the pattern of rGH use in Italian clinical practice. This study aimed at exploring the pattern of biosimilar and originator rGH use in six Italian centers, where different policy interventions promoted biosimilar use.
This population-based, drug-utilization study was conducted in the years 2009-2014, using administrative databases of Umbria, Tuscany, and Lazio Regions and Local Health Units of Caserta, Treviso, and Palermo. Naïve rGH users were characterized, and prevalence of use and discontinuation were assessed over time.
Among 6,785 patients treated with rGH during the study years, 4,493 (66.2%) were naïve users (males/females = 1.3), mostly affected by GH deficiency. The prevalence of rGH use increased from 2009 to 2010, remaining stable thereafter, but it was heterogeneous across centers (twofold higher prevalence of use in center n.2 than centers n.4 and 1 in 2014). Biosimilar rGH uptake increased over time but was low (7.8% in 2014) and heterogeneous as well. Discontinuation of rGH therapy occurred in 54.0% of naïve users, more frequently in females than males (58.1 vs. 50.9%). During the first year of treatment, discontinuation was frequent (39.9%), but no statistically significant differences were observed in treatment persistence for biosimilar vs. originator rGH ( > 0.05).
Geographical heterogeneity in the prevalence of rGH use was observed. Similarly, the biosimilar rGH uptake was low and variable across centers. Post-marketing monitoring is required to continuously monitor the benefit-risk profile of rGH, thus guaranteeing greater savings than only promoting lowest cost rGH.
生长激素[重组生长激素(rGH)]在儿童和成人中被批准用于多种涉及生长障碍的病症,自2006年起意大利就有相应的生物类似药。意大利临床实践中关于rGH使用模式尚无基于人群的数据。本研究旨在探索在意大利六个中心生物类似药和原研rGH的使用模式,在这些中心采取了不同的政策干预措施来促进生物类似药的使用。
这项基于人群的药物利用研究于2009年至2014年进行,使用翁布里亚、托斯卡纳和拉齐奥地区以及卡塞塔、特雷维索和巴勒莫地方卫生单位的行政数据库。对初治rGH使用者进行特征描述,并评估随时间推移的使用患病率和停药情况。
在研究期间接受rGH治疗的6785例患者中,4493例(66.2%)为初治使用者(男性/女性=1.3),主要患有生长激素缺乏症。rGH的使用患病率从2009年到2010年有所增加,此后保持稳定,但各中心之间存在差异(2014年中心2的使用患病率比中心4和中心1高出两倍)。生物类似药rGH的采用率随时间增加,但较低(2014年为7.8%)且也存在差异。54.0%的初治使用者停止了rGH治疗女性比男性更频繁(58.1%对50.9%)。在治疗的第一年,停药很常见(39.9%),但生物类似药与原研rGH在治疗持续时间上未观察到统计学显著差异(P>0.05)。
观察到rGH使用患病率存在地理差异。同样,生物类似药rGH的采用率较低且各中心之间存在差异。需要进行上市后监测以持续监测rGH的获益风险状况,从而保证比仅推广成本最低的rGH能节省更多费用。