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地拉罗司治疗骨髓增生异常综合征输血所致铁过载后的造血恢复情况

Hematopoietic recovery after administration of deferasirox for transfusional iron overload in a case of myelodysplastic syndrome.

作者信息

OKABE Hiroshi, SUZUKI Takahiro, OMORI Tsukasa, MORI Masaki, UEHARA Eisuke, HATANO Kaoru, UEDA Masuzu, MATSUYAMA Tomohiro, TOSHIMA Masaki, QZAKI Katsutoshi, NAGAI Tadashi, MUROI Kazuo, OZAWA Keiya

机构信息

Division of Hematology, Department of Medicine, Jichi Medical University.

出版信息

Rinsho Ketsueki. 2009 Nov;50(11):1626-9.

Abstract

Deferasirox (DFX) is a newly developed oral iron chelator that enables effective chelation with once daily administration. We describe here a case of transfusional-iron overloaded patient who experienced hematopoietic recovery after DFX administration. A 75-year-old woman with iron overload, who had been diagnosed with MDS (RCMD) and had received a transfusion of red blood cells and platelets regularly for 3 years, enrolled in the phase I clinical trial of ICL670 (DFX) in Japan. DFX administration steadily decreased her serum ferritin levels and chelated overloaded iron effectively. Interestingly, a year after initiation of the trial, she needed fewer blood transfusions, and no more transfusions after the 17th month of the trial. Even after suspending transfusions, her hemoglobin level and platelet count increased continuously, and she now has stable disease without blood transfusions. She has not received any specific treatment for MDS during this period. Examination of the bone marrow aspirates in the 35th month revealed dysplastic cells, indicating no remarkable change in the state of MDS. This case suggests that excess iron hampers hematopoiesis and that adequate iron chelation may improve hematological data in some iron-overloaded patients.

摘要

地拉罗司(DFX)是一种新开发的口服铁螯合剂,每日服用一次即可实现有效螯合。我们在此描述一例输血性铁过载患者,在服用DFX后出现造血恢复。一名75岁的铁过载女性,被诊断为骨髓增生异常综合征(RCMD),并定期接受红细胞和血小板输血3年,参加了日本ICL670(DFX)的I期临床试验。服用DFX后,她的血清铁蛋白水平稳步下降,有效螯合了过载的铁。有趣的是,试验开始一年后,她需要的输血次数减少,在试验第17个月后不再输血。即使在停止输血后,她的血红蛋白水平和血小板计数仍持续上升,现在病情稳定,无需输血。在此期间,她未接受任何针对骨髓增生异常综合征的特殊治疗。在第35个月对骨髓穿刺物的检查显示有发育异常细胞,表明骨髓增生异常综合征的状态没有明显变化。该病例表明,过量的铁会阻碍造血,而适当的铁螯合可能会改善一些铁过载患者的血液学数据。

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