Rapid withdrawal of voxelotor can precipitate sickle cell disease related crisis.

IF 3 3区 医学 Q2 HEMATOLOGY
Salam Alkindi, Ahmed Al Subhi, Anil Pathare
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引用次数: 0

Abstract

Sickle cell disease (SCD) is an inherited disorder characterized by abnormal mutation leading to formation of sickle red blood cells. The initial step is the formation of polymers and precipitation of Hemoglobin within the cell. voxelotor is a novel anti-polymerization drug approved for treatment of patients with SCD, resulting in improved hemoglobin level. Recently its clinical development was suspended, as concerns were raised regarding its safety and efficacy. We have evaluated 11 patients who were stable, on voxelotor for a mean period of 191 weeks (range, 8-369). We observed that upon its withdrawal, 8 patients (73%) showed a rapid onset of vaso-occlusive crisis, within a median of 4.7 days, precipitating hemolysis, with a significant drop of Hb, raised reticulocytes, bilirubin, and lactic dehydrogenase. Also, one patient (9.1%) developed acute chest syndrome, whereas five (45.5%) patients needed blood transfusions. Our data confirms that rapid withdrawal of voxelotor could precipitate severe SCD-related crisis.

迅速停药可引起镰状细胞病相关危象。
镰状细胞病(SCD)是一种以异常突变导致镰状红细胞形成为特征的遗传性疾病。最初的步骤是在细胞内形成聚合物和沉淀血红蛋白。voxelotor是一种新型抗聚合药物,被批准用于治疗SCD患者,可改善血红蛋白水平。最近,由于对其安全性和有效性的担忧,其临床开发被暂停。我们评估了11例使用voxelotor稳定的患者,平均时间为191周(范围8-369周)。我们观察到,在停药后,8例患者(73%)出现血管闭塞危象的快速发作,中位时间为4.7天,伴有溶血,血红蛋白显著下降,网状红细胞、胆红素和乳酸脱氢酶升高。1例(9.1%)出现急性胸综合征,5例(45.5%)需要输血。我们的数据证实,快速停用voxelotor可能会引发严重的scd相关危机。
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来源期刊
Annals of Hematology
Annals of Hematology 医学-血液学
CiteScore
5.60
自引率
2.90%
发文量
304
审稿时长
2 months
期刊介绍: Annals of Hematology covers the whole spectrum of clinical and experimental hematology, hemostaseology, blood transfusion, and related aspects of medical oncology, including diagnosis and treatment of leukemias, lymphatic neoplasias and solid tumors, and transplantation of hematopoietic stem cells. Coverage includes general aspects of oncology, molecular biology and immunology as pertinent to problems of human blood disease. The journal is associated with the German Society for Hematology and Medical Oncology, and the Austrian Society for Hematology and Oncology.
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