Dipartimento di oncoematologia, U.O.C. Centro delle Microcitemie A. Mastrobuoni, Azienda Ospedaliera di Rilievo Nazionale A. Cardarelli, Via A. Cardarelli 9, Naples, Italy.
Expert Opin Drug Saf. 2010 Nov;9(6):875-81. doi: 10.1517/14740338.2010.510831.
Although IFN therapy is known to cause neutropenia, data on the risk of deferiprone (DFP)-induced haematological complications in patients receiving IFN are lacking.
This was a retrospective single-centre study to assess the association between exposure to IFN for hepatitis C virus treatment and haematological side effects of DFP therapy in patients with thalassemia major and intermedia using a large database spanning 2001 – 2008. During observation time, a total of 66 patients, including 63 affected by thalassemia major and 3 by thalassemia intermedia, were treated with chelation DFP-based regimens. A subset of 25 patients was treated at least for 3 months also with IFN (6 were cotreated and 19 were pretreated).
Overall, the incidence of neutropenia and agranulocytosis was 9.83 and 1.14/100 patient/year, respectively. Receipt of IFN was significantly associated with increased risk of haematological complications of DFP therapy: among patients receiving IFN, 48 and 12% experienced at least one episode of neutropenia and agranulocytosis, respectively.
These results suggest that IFN therapy may increase the risk of complications of DFP-based iron chelation therapy in patients with thalassemia. Further research is needed to assess whether the association observed in this retrospective single-centre observational study is due to IFN or other factors.
虽然干扰素(IFN)治疗已知会导致中性粒细胞减少症,但缺乏接受 IFN 治疗的患者使用去铁酮(DFP)治疗引起血液学并发症的风险数据。
这是一项回顾性单中心研究,使用跨越 2001-2008 年的大型数据库,评估了接受丙型肝炎病毒治疗用 IFN 暴露与重型和中间型地中海贫血患者 DFP 治疗的血液学副作用之间的关联。在观察期间,共有 66 名患者接受了基于螯合的 DFP 方案治疗,其中 63 名患有重型地中海贫血,3 名患有中间型地中海贫血。其中一组 25 名患者至少接受了 3 个月的 IFN 治疗(6 名联合治疗,19 名预先治疗)。
总体而言,中性粒细胞减少症和粒细胞缺乏症的发生率分别为 9.83 和 1.14/100 患者/年。接受 IFN 治疗与 DFP 治疗血液学并发症的风险增加显著相关:接受 IFN 的患者中,分别有 48%和 12%至少经历了一次中性粒细胞减少症和粒细胞缺乏症。
这些结果表明,IFN 治疗可能会增加地中海贫血患者接受 DFP 为基础的铁螯合治疗的并发症风险。需要进一步研究以评估在这项回顾性单中心观察性研究中观察到的关联是否归因于 IFN 或其他因素。