抗人T淋巴细胞猪免疫球蛋白联合环孢素作为治疗中国严重再生障碍性贫血的一线免疫抑制药物:一项大型单中心、10年回顾性研究

IF 3.4 3区 医学 Q2 HEMATOLOGY
Wenrui Yang, Xu Liu, Xin Zhao, Li Zhang, Guangxin Peng, Lei Ye, Kang Zhou, Yuan Li, Jianping Li, Huihui Fan, Yang Yang, Youzhen Xiong, Liping Jing, Fengkui Zhang
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引用次数: 2

摘要

背景:自2009年以来,抗人T淋巴细胞猪免疫球蛋白(p-ATG)已成为中国严重再生障碍性贫血(SAA)患者免疫抑制治疗(IST)中最常用的ATG制剂。目的:本研究旨在评估2010年至2019年期间接受p-ATG联合环孢素(CsA)作为一线治疗的大型SAA患者的早期血液学反应和长期预后。设计:这是一项针对医疗记录的单中心回顾性研究。方法:分析2010 - 2019年我科1023例连续接受p-ATG联合CsA一线IST治疗的获得性再生障碍性贫血(AA)患者的资料。结果:患者中位年龄24(4 ~ 75)岁,中位随访时间57.2个月(3天~ 137.5个月)。早期死亡率为2.8%,中位死亡时间为0.9个月(3天-2.9个月)。3个月和6个月的总有效率分别为40.6%和56.1%。5年累积复发率和克隆进化率分别为9.0%[95%可信区间(CI) = 4.2 ~ 16.0%]和4.5% (95% CI = 1.4 ~ 10.6%)。5年总生存率(OS)和无事件生存率分别为83.7% (95% CI = 81.1-86.0%)和50.4% (95% CI = 47.1-53.5%)。结论:p-ATG联合CsA治疗AA有效、安全,在h-ATG无法应用的地区,p-ATG可作为标准IST方案的替代ATG制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Antihuman T lymphocyte porcine immunoglobulin combined with cyclosporine as first-line immunosuppressive therapy for severe aplastic anemia in China: a large single-center, 10-year retrospective study.

Antihuman T lymphocyte porcine immunoglobulin combined with cyclosporine as first-line immunosuppressive therapy for severe aplastic anemia in China: a large single-center, 10-year retrospective study.

Antihuman T lymphocyte porcine immunoglobulin combined with cyclosporine as first-line immunosuppressive therapy for severe aplastic anemia in China: a large single-center, 10-year retrospective study.

Antihuman T lymphocyte porcine immunoglobulin combined with cyclosporine as first-line immunosuppressive therapy for severe aplastic anemia in China: a large single-center, 10-year retrospective study.

Background: Antihuman T lymphocyte porcine immunoglobulin (p-ATG) has been the most common ATG preparation in immunosuppressive therapy (IST) in Chinese patients with severe aplastic anemia (SAA) since 2009.

Objectives: This study aimed to evaluate the early hematologic response and long-term outcomes of a large cohort of patients with SAA who received p-ATG plus cyclosporine (CsA) as first-line therapy from 2010 to 2019.

Design: This is a single-center retrospective study of medical records.

Methods: We analyzed the data of 1023 consecutive patients with acquired aplastic anemia (AA) who underwent p-ATG combined with CsA as a first-line IST treatment from 2010 to 2019 at our department.

Results: The median age of the patients was 24 (4-75) years, and the median follow-up time was 57.2 months (3 days-137.5 months). There was an early mortality rate of 2.8% with a median death time of 0.9 months (3 days-2.9 months). The overall response rates were 40.6% and 56.1% at 3 and 6 months, respectively. The 5-year cumulative incidences of relapse and clonal evolution were 9.0% [95% confidence interval (CI) = 4.2-16.0%] and 4.5% (95% CI = 1.4-10.6%), respectively. The 5-year overall survival (OS) and event-free survival rates were 83.7% (95% CI = 81.1-86.0%) and 50.4% (95% CI = 47.1-53.5%), respectively.

Conclusion: p-ATG combined with CsA for the treatment of AA is effective and safe, and p-ATG can be used as an alternative ATG preparation for the standard IST regimen in areas in which h-ATG is not available.

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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
54
审稿时长
7 weeks
期刊介绍: Therapeutic Advances in Hematology delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of hematology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in hematology, providing a forum in print and online for publishing the highest quality articles in this area.
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