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在日本,免疫抑制治疗初治的再生障碍性贫血患者中,联合用艾曲波帕与兔抗胸腺细胞球蛋白/环孢素 A。

Eltrombopag in Combination with Rabbit Anti-thymocyte Globulin/Cyclosporine A in Immunosuppressive Therapy-naïve Patients with Aplastic Anemia in Japan.

机构信息

Department of Hematology, Japanese Red Cross Osaka Hospital, Japan.

Department of Hematology, University of Tsukuba, Japan.

出版信息

Intern Med. 2021 Apr 15;60(8):1159-1168. doi: 10.2169/internalmedicine.6063-20. Epub 2020 Nov 23.

Abstract

Objective In Japan, immunosuppressive therapy (IST) with anti-thymocyte globulin (ATG), and cyclosporine A (CsA) is the standard of care in patients with aplastic anemia (AA) who are not indicated for stem-cell transplantation, although some patients may experience relapse. This study assessed the efficacy and safety of eltrombopag in combination with rabbit-ATG/CsA in IST-naïve patients with non-severe or severe AA in Japan. Methods In this non-randomized, open-label, single-arm, phase II study, rabbit-ATG/CsA and eltrombopag were initiated on Days 1 and 15 (±3 days), respectively, and continued for ≥26 weeks; rabbit-ATG was given for 5 days (Days 1 to 5). The primary endpoint was the overall response rate (ORR) at Week 26. Patients Patients with AA who were IST-naïve and ≤70 years old or between 71 and 75 years old based on the recommendation of the investigator were enrolled in Japan. Results Of the 11 enrolled patients, 10 started treatment with eltrombopag. The ORRs at Weeks 26 and 52 were 70.0% and 60.0%, respectively. The ORR at Week 26 was 100% (all 3 patients) in patients with non-severe AA and 57.1% (4/7) in patients with severe AA. Among transfusion-dependent patients, 66.7% (4/6) and 62.5% (5/8) became red blood cell- and platelet-transfusion independent, respectively. The most common adverse events were nausea and headache. No deaths or hematologic malignancies were reported. A cytogenetic abnormality was reported in one patient. Conclusion This study confirmed the clinical benefit of eltrombopag plus rabbit-ATG/CsA in IST-naïve patients with non-severe or severe AA in Japan.

摘要

目的

在日本,对于不适合进行干细胞移植的再生障碍性贫血(AA)患者,免疫抑制疗法(IST)联合抗胸腺细胞球蛋白(ATG)和环孢素 A(CsA)是标准治疗方案,尽管部分患者可能会出现复发。本研究评估了艾曲波帕联合兔源 ATG/CsA 在日本初治的非重型或重型 AA 患者中的疗效和安全性。

方法

这是一项非随机、开放标签、单臂、II 期研究,在第 1 天和第 15 天(±3 天)分别起始兔源 ATG/CsA 和艾曲波帕治疗,持续时间≥26 周;兔源 ATG 治疗 5 天(第 1 天至第 5 天)。主要终点为第 26 周的总体缓解率(ORR)。

患者

在日本,纳入了年龄≤70 岁或 71-75 岁(基于研究者的建议)且初治的 AA 患者。

结果

11 例患者中,有 10 例开始接受艾曲波帕治疗。第 26 周和第 52 周的 ORR 分别为 70.0%和 60.0%。非重型 AA 患者的 ORR 在第 26 周为 100%(3 例均为完全缓解),重型 AA 患者为 57.1%(4/7)。在依赖输血的患者中,分别有 66.7%(4/6)和 62.5%(5/8)实现红细胞和血小板输血独立。最常见的不良反应为恶心和头痛。未报告死亡或血液系统恶性肿瘤。一名患者出现细胞遗传学异常。

结论

本研究证实了在日本,艾曲波帕联合兔源 ATG/CsA 在初治的非重型或重型 AA 患者中具有临床获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5cc/8112980/f036f7227e35/1349-7235-60-1159-g001.jpg

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