• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.4084/MJHID.2014.042
PMID:24959339
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4063602/
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/4063602/56de6a0f8c67/mjhid-6-1-e2014042f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/651d/4063602/4c1ab7b07a9f/mjhid-6-1-e2014042f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/651d/4063602/545b8f321d7c/mjhid-6-1-e2014042f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/651d/4063602/8a3912a165be/mjhid-6-1-e2014042f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/651d/4063602/56de6a0f8c67/mjhid-6-1-e2014042f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/651d/4063602/4c1ab7b07a9f/mjhid-6-1-e2014042f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/651d/4063602/545b8f321d7c/mjhid-6-1-e2014042f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/651d/4063602/8a3912a165be/mjhid-6-1-e2014042f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/651d/4063602/56de6a0f8c67/mjhid-6-1-e2014042f4.jpg

相似文献

1
Iron chelation therapy with deferasirox in the management of iron overload in primary myelofibrosis.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
Mediterr J Hematol Infect Dis. 2014 Jun 1;6(1):e2014042. doi: 10.4084/MJHID.2014.042. eCollection 2014.
2
Deferasirox for transfusion-dependent patients with myelodysplastic syndromes: safety, efficacy, and beyond (GIMEMA MDS0306 Trial).地拉罗司用于依赖输血的骨髓增生异常综合征患者:安全性、疗效及其他(GIMEMA MDS0306试验)
Eur J Haematol. 2014 Jun;92(6):527-36. doi: 10.1111/ejh.12300. Epub 2014 Apr 10.
3
Results from a 1-year, open-label, single arm, multi-center trial evaluating the efficacy and safety of oral Deferasirox in patients diagnosed with low and int-1 risk myelodysplastic syndrome (MDS) and transfusion-dependent iron overload.一项为期 1 年、开放性、单臂、多中心试验的结果,评估了口服地拉罗司在低危和中危-1 风险骨髓增生异常综合征(MDS)和输血依赖型铁过载患者中的疗效和安全性。
Ann Hematol. 2013 Jan;92(2):191-8. doi: 10.1007/s00277-012-1594-z. Epub 2012 Oct 17.
4
Improved survival in red blood cell transfusion dependent patients with primary myelofibrosis (PMF) receiving iron chelation therapy.依赖红细胞输血的原发性骨髓纤维化(PMF)患者接受铁螯合治疗后生存改善。
Hematol Oncol. 2010 Mar;28(1):40-8. doi: 10.1002/hon.902.
5
Optimising management of deferasirox therapy for patients with transfusion-dependent thalassaemia and lower-risk myelodysplastic syndromes.优化依赖输血的地中海贫血和低危骨髓增生异常综合征患者的地拉罗司治疗管理。
Eur J Haematol. 2018 Sep;101(3):272-282. doi: 10.1111/ejh.13111. Epub 2018 Jul 27.
6
Deferasirox treatment improved the hemoglobin level and decreased transfusion requirements in four patients with the myelodysplastic syndrome and primary myelofibrosis.地拉罗司治疗改善了4例骨髓增生异常综合征和原发性骨髓纤维化患者的血红蛋白水平,并减少了输血需求。
Acta Haematol. 2008;120(2):70-4. doi: 10.1159/000158631. Epub 2008 Oct 1.
7
Clinical consequences of iron overload in patients with myelodysplastic syndromes: the case for iron chelation therapy.骨髓增生异常综合征患者铁过载的临床后果:铁螯合疗法的情况
Expert Rev Hematol. 2018 Jul;11(7):577-586. doi: 10.1080/17474086.2018.1486188. Epub 2018 Jun 19.
8
Prospective evaluation of the effect of deferasirox on hematologic response in transfusion-dependent patients with low-risk MDS and iron overload.去铁胺对低危骨髓增生异常综合征及铁过载的输血依赖患者血液学反应影响的前瞻性评估
Eur J Haematol. 2018 May 2. doi: 10.1111/ejh.13088.
9
Iron Chelation in Transfusion-Dependent Patients With Low- to Intermediate-1-Risk Myelodysplastic Syndromes: A Randomized Trial.输血依赖型低危至中危-1 级骨髓增生异常综合征患者的铁螯合治疗:一项随机试验。
Ann Intern Med. 2020 Apr 21;172(8):513-522. doi: 10.7326/M19-0916. Epub 2020 Mar 24.
10
Adequate iron chelation therapy for at least six months improves survival in transfusion-dependent patients with lower risk myelodysplastic syndromes.充分的铁螯合治疗至少 6 个月可改善输血依赖型低危骨髓增生异常综合征患者的生存。
Leuk Res. 2014 May;38(5):557-63. doi: 10.1016/j.leukres.2014.02.003. Epub 2014 Feb 14.

引用本文的文献

1
Iron overload disorders.铁过载疾病。
Hepatol Commun. 2022 Aug;6(8):1842-1854. doi: 10.1002/hep4.2012. Epub 2022 Jun 14.
2
The relationship between serum ferritin level and fibrosis and splenomegaly in myelofibrosis.骨髓纤维化中血清铁蛋白水平与纤维化及脾肿大的关系。
Am J Blood Res. 2020 Dec 15;10(6):345-350. eCollection 2020.
3
The role of allogeneic stem-cell transplant in myelofibrosis in the era of JAK inhibitors: a case-based review.JAK抑制剂时代异基因干细胞移植在骨髓纤维化中的作用:基于病例的综述

本文引用的文献

1
Mayor erythropoietic response after deferasirox treatment in a transfusion-dependent anemic patient with primary myelofibrosis.在一名依赖输血的原发性骨髓纤维化贫血患者中,地拉罗司治疗后的主要红细胞生成反应。
Case Rep Hematol. 2013;2013:520712. doi: 10.1155/2013/520712. Epub 2013 Nov 6.
2
Deferasirox: appraisal of safety and efficacy in long-term therapy.地拉罗司:长期治疗中的安全性与有效性评估
J Blood Med. 2013 Aug 5;4:101-10. doi: 10.2147/JBM.S35478. eCollection 2013.
3
Haematological improvement as a beneficial effect during deferasirox treatment in transfusion-dependent patients with myelodysplastic syndrome.
Bone Marrow Transplant. 2020 Apr;55(4):708-716. doi: 10.1038/s41409-019-0683-1. Epub 2019 Sep 18.
4
Treatment of Myelofibrosis: Old and New Strategies.骨髓纤维化的治疗:新旧策略
Clin Med Insights Blood Disord. 2017 Mar 8;10:1179545X17695233. doi: 10.1177/1179545X17695233. eCollection 2017.
5
[MRI monitoring in diagnosis and follow-up of iron overload].[磁共振成像监测在铁过载诊断及随访中的应用]
Zhonghua Xue Ye Xue Za Zhi. 2015 Apr;36(4):302-6. doi: 10.3760/cma.j.issn.0253-2727.2015.04.009.
6
Historical views, conventional approaches, and evolving management strategies for myeloproliferative neoplasms.骨髓增殖性肿瘤的历史观点、传统方法及不断演变的管理策略
J Natl Compr Canc Netw. 2015 Apr;13(4):424-34. doi: 10.6004/jnccn.2015.0058.
对于依赖输血的骨髓增生异常综合征患者,去铁胺治疗期间血液学改善是一种有益效果。
Blood Transfus. 2014 Jan;12 Suppl 1(Suppl 1):s162-3. doi: 10.2450/2013.0005-13. Epub 2013 Apr 15.
4
Hematologic responses in patients with aplastic anemia treated with deferasirox: a post hoc analysis from the EPIC study.贫血再生障碍性治疗患者的血液学反应:来自 EPIC 研究的事后分析。
Haematologica. 2013 Jul;98(7):1045-8. doi: 10.3324/haematol.2012.077669. Epub 2013 Apr 12.
5
A comprehensive review and analysis of the effect of ruxolitinib therapy on the survival of patients with myelofibrosis.对芦可替尼治疗骨髓纤维化患者生存影响的全面回顾和分析。
Blood. 2013 Jun 13;121(24):4832-7. doi: 10.1182/blood-2013-02-482232. Epub 2013 Apr 9.
6
Loss of transfusion dependency following deferasirox treatment of iron overload in a woman with myelofibrosis and spherocytosis - a case report.地拉罗司治疗骨髓纤维化合并球形红细胞增多症女性铁过载后输血依赖的丧失——病例报告
Onkologie. 2013;36(4):205-8. doi: 10.1159/000349939. Epub 2013 Mar 18.
7
Efficacy and safety of deferasirox in myelodysplastic syndromes.地拉罗司治疗骨髓增生异常综合征的疗效和安全性。
Ann Hematol. 2013 Jul;92(7):863-70. doi: 10.1007/s00277-013-1703-7. Epub 2013 Feb 17.
8
Primary myelofibrosis: 2013 update on diagnosis, risk-stratification, and management.原发性骨髓纤维化:2013 年诊断、风险分层和治疗更新。
Am J Hematol. 2013 Feb;88(2):141-50. doi: 10.1002/ajh.23384.
9
How I treat transfusional iron overload.如何治疗输血引起的铁过载
Blood. 2012 Nov 1;120(18):3657-69. doi: 10.1182/blood-2012-05-370098. Epub 2012 Aug 23.
10
An update on iron chelation therapy.铁螯合疗法的最新进展。
Blood Transfus. 2012 Oct;10(4):411-22. doi: 10.2450/2012.0008-12. Epub 2012 Jun 27.