Efficacy of Epoetin Alfa in Managing Symptomatic Anaemia in Low-Risk Myelodysplastic Syndromes: A Retrospective Analysis.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Cureus Pub Date : 2024-10-27 eCollection Date: 2024-10-01 DOI:10.7759/cureus.72460
Mohamed Aboulela, Angela Collins
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Abstract

Background Myelodysplastic syndromes (MDS) are clonal myeloid disorders characterised by ineffective haematopoiesis, leading to anaemia that often requires dependence on red blood cell (RBC) transfusions. Epoetin alfa (Eprex®) is now a mainstay in the management of symptomatic anaemia in low-risk MDS patients, reducing transfusion dependence and improving the quality of life in this patient group. Objective This retrospective study aimed to assess the efficacy of epoetin alfa in treating symptomatic anaemia in low-risk MDS patients, focusing on transfusion independence and its relationship with baseline erythropoietin (EPO) levels and haemoglobin (Hb) response. Methods Data from 56 patients with low-risk MDS treated with epoetin alfa at Norfolk and Norwich University Hospital, Norwich, United Kingdom, between 2018 and 2023 were retrospectively analysed. Baseline EPO levels, transfusion history, Hb response, and the duration of transfusion independence were assessed. Statistical analyses were performed to evaluate the correlation between baseline characteristics and treatment outcomes. Results Among the patients, 98.2% had baseline EPO levels below the 500 IU/L threshold, with a median EPO level of 74.3 IU/L. Following an eight-week trial of 30,000 units of epoetin-alfa, 41.1% of patients showed improved Hb levels, 41.1% maintained stable Hb levels, and 17.9% experienced a decline. A significant correlation was found between lower baseline EPO levels (<250 IU/L) and a positive treatment response (p = 0.0065). Additionally, patients who required fewer transfusions before treatment had longer durations of transfusion independence (correlation coefficient = -0.40, p = 0.015). Dose escalation to 60,000 units provided a benefit to 53.3% of patients with initially stable Hb levels. The average duration of transfusion independence was 8.1 months, and patients with improved Hb levels had the longest periods of transfusion independence (p = 0.005). Conclusion Epoetin alfa is an effective therapy for managing symptomatic anaemia in low-risk MDS patients. This study highlights its efficacy and provides valuable predictive information, particularly showing that patients with lower baseline EPO levels are more likely to respond to treatment. While prior transfusion dependence did not significantly predict response to therapy in this cohort, it was associated with the duration of transfusion independence.

Epoetin Alfa 在治疗低风险骨髓增生异常综合征症状性贫血中的疗效:回顾性分析
背景 骨髓增生异常综合征(MDS)是一种克隆性骨髓疾病,其特点是造血功能低下,导致贫血,常常需要依赖输注红细胞(RBC)。目前,Epoetin alfa(Eprex®)已成为治疗低危 MDS 患者症状性贫血的主要药物,可减少对输血的依赖性,提高这类患者的生活质量。目的 本回顾性研究旨在评估epoetin alfa治疗低危MDS患者症状性贫血的疗效,重点关注输血独立性及其与基线促红细胞生成素(EPO)水平和血红蛋白(Hb)反应的关系。方法 回顾性分析了英国诺福克和诺里奇大学医院在2018年至2023年期间用环氧乙烷α治疗的56名低风险MDS患者的数据。评估了基线 EPO 水平、输血史、Hb 反应和输血独立性持续时间。进行了统计分析,以评估基线特征与治疗结果之间的相关性。结果 98.2% 的患者 EPO 水平低于 500 IU/L 临界值,EPO 水平中位数为 74.3 IU/L。在接受为期八周的 30,000 单位环孢素-阿法治疗后,41.1% 的患者血红蛋白水平有所改善,41.1% 的患者血红蛋白水平保持稳定,17.9% 的患者血红蛋白水平有所下降。研究发现,较低的基线 EPO 含量与 Hb 含量之间存在明显的相关性 (
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