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用地拉罗司进行铁螯合疗法治疗原发性骨髓纤维化中的铁过载

Iron chelation therapy with deferasirox in the management of iron overload in primary myelofibrosis.

作者信息

Elli Elena Maria, Belotti Angelo, Aroldi Andrea, Parma Matteo, Pioltelli Pietro, Pogliani Enrico Maria

机构信息

Hematology Division, San Gerardo Hospital, Monza, Italy.

出版信息

Mediterr J Hematol Infect Dis. 2014 Jun 1;6(1):e2014042. doi: 10.4084/MJHID.2014.042. eCollection 2014.

Abstract

Deferasirox (DSX) is the principal option currently available for iron-chelation-therapy (ICT), principally in the management of myelodysplastic syndromes (MDS), while in primary myelofibrosis (PMF) the expertise is limited. We analyzed our experience in 10 PMF with transfusion-dependent anemia, treated with DSX from September 2010 to December 2013. The median dose tolerated of DSX was 750 mg/day (10 mg/kg/day), with 3 transient interruption of treatment for drug-related adverse events (AEs) and 3 definitive discontinuation for grade 3/4 AEs. According to IWG 2006 criteria, erythroid responses with DSX were observed in 4/10 patients (40%), 2 of them (20%) obtaining transfusion independence. Absolute changes in median serum ferritin levels (Delta ferritin) were greater in hematologic responder (HR) compared with non-responder (NR) patients, already at 6 months of ICT respect to baseline. Our preliminary data open new insights regarding the benefit of ICT not only in MDS, but also in PMF with the possibility to obtain an erythroid response, overall in 40 % of patients. HR patients receiving DSX seem to have a better survival and a lower incidence of leukemic transformation (PMF-BP). Delta ferritin evaluation at 6 months could represent a significant predictor for a different survival and PMF-BP. However, the tolerability of the drug seems to be lower compared to MDS, both in terms of lower median tolerated dose and for higher frequency of discontinuation for AEs. The biological mechanism of action of DSX in chronic myeloproliferative setting through an independent NF-κB inhibition could be involved, but further investigations are required.

摘要

地拉罗司(DSX)是目前铁螯合疗法(ICT)的主要选择,主要用于治疗骨髓增生异常综合征(MDS),而在原发性骨髓纤维化(PMF)方面,相关经验有限。我们分析了2010年9月至2013年12月期间使用DSX治疗的10例输血依赖型贫血的PMF患者的经验。DSX的中位耐受剂量为750毫克/天(10毫克/千克/天),3例因药物相关不良事件(AE)短暂中断治疗,3例因3/4级AE最终停药。根据2006年IWG标准,10例患者中有4例(40%)出现了DSX诱导的红系反应,其中2例(20%)实现了输血独立。与未缓解者(NR)相比,血液学缓解者(HR)在ICT治疗6个月时相对于基线的中位血清铁蛋白水平绝对变化(Δ铁蛋白)更大。我们的初步数据为ICT的益处提供了新的见解,不仅在MDS中,而且在PMF中也有可能获得红系反应,总体上40%的患者有效。接受DSX治疗的HR患者似乎有更好的生存率和更低的白血病转化(PMF-BP)发生率。6个月时的Δ铁蛋白评估可能是不同生存率和PMF-BP的重要预测指标。然而,与MDS相比,该药物的耐受性似乎较低,无论是中位耐受剂量较低还是因AE停药的频率较高。DSX在慢性骨髓增殖性疾病中的生物学作用机制可能涉及通过独立抑制NF-κB,但仍需进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/651d/4063602/4c1ab7b07a9f/mjhid-6-1-e2014042f1.jpg

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