用猪抗淋巴细胞球蛋白加环孢素,加或不加血小板生成素受体激动剂治疗重型再生障碍性贫血的长期疗效和安全性:一项双中心回顾性研究。

IF 2.3 4区 医学 Q2 HEMATOLOGY Expert Review of Hematology Pub Date : 2024-04-01 Epub Date: 2024-05-08 DOI:10.1080/17474086.2024.2350527
Shan Xu, Yue Xiao, Xinquan Liang, Yan Lu, Mingyang Deng
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引用次数: 0

摘要

背景:猪抗淋巴细胞球蛋白(p-ALG)联合环孢素(CsA)已被普遍用于重型再生障碍性贫血(SAA)患者,但有关p-ALG与血小板生成素受体激动剂(TPO-RA)联合应用的研究却很少:我们回顾性分析了2014年至2023年接受p-ALG加CsA、加或不加TPO-RA治疗的85名确诊SAA患者的数据:3个月和6个月时的总应答率分别为55.3%和65.9%,TPO-RA组3个月和6个月时的总应答率分别为66.7%和72.3%,无TPO-RA组3个月和6个月时的总应答率分别为27.8%和55.6%。在多变量分析中,基线血小板计数> 10×109/L是6个月时良好反应的简单预测因子(P = 0.015)。所有患者的中位随访时间为 39 个月(0.4 ~ 104 个月),5 年总生存(OS)率为 90.6% [95% CI = 82.1-95.2%],无失败生存(FFS)率为 68.9% [95% CI = 56.6-78.4%]。6个月内血液学反应是预测无失败生存率的独立阳性指标(P = 0.000)。结论:p-ALG联合CsA是SAA患者的有效选择。
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The long-term outcomes and safety of severe aplastic anemia treated with porcine antilymphocyte globulin plus cyclosporine, with or without thrombopoietin receptor agonists: a double-center retrospective study.

Background: Porcine antilymphocyte globulin (p-ALG) combined with cyclosporine (CsA) has been commonly used for severe aplastic anemia (SAA) patients, but few studies on the combination of p-ALG and thrombopoietin receptor agonist (TPO-RA).

Research design and methods: We retrospectively analyzed the data of 85 people with diagnosed SAA who underwent p-ALG plus CsA, with or without TPO-RA from 2014 to 2023.

Results: The overall response rates were 55.3% and 65.9% at 3 and 6 months, and the TPO-RA group were 66.7% and 72.3% at 3 and 6 months, without TPO-RA group were 27.8% and 55.6%. In multivariate analysis, baseline platelet count of > 10 × 109/L was a simple predictor of favorable response at 6 months (p = 0.015). The median follow-up time for all patients was 39 months (range 0.4 ~ 104), the 5-year overall survival (OS) rate was 90.6% [95% CI = 82.1-95.2%], and the failure-free survival (FFS) rate was 68.9% [95% CI = 56.6-78.4%]. Having hematologic responses in 6 months was an independent positive predictor for FFS (p = 0.000). Twelve patients (14.1%) suffered from serum sickness, and 9.5% of patients had mild hepatic impairment.

Conclusions: p-ALG along with CsA is an effective choice for patients with SAA. p-ALG combined with TPO-RA may contribute to the early restoration of hematopoiesis.

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来源期刊
CiteScore
4.70
自引率
3.60%
发文量
98
审稿时长
6-12 weeks
期刊介绍: Advanced molecular research techniques have transformed hematology in recent years. With improved understanding of hematologic diseases, we now have the opportunity to research and evaluate new biological therapies, new drugs and drug combinations, new treatment schedules and novel approaches including stem cell transplantation. We can also expect proteomics, molecular genetics and biomarker research to facilitate new diagnostic approaches and the identification of appropriate therapies. Further advances in our knowledge regarding the formation and function of blood cells and blood-forming tissues should ensue, and it will be a major challenge for hematologists to adopt these new paradigms and develop integrated strategies to define the best possible patient care. Expert Review of Hematology (1747-4086) puts these advances in context and explores how they will translate directly into clinical practice.
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