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一种新型重组人血小板生成素治疗异基因造血干细胞移植后长期孤立性血小板减少症。

A novel recombinant human thrombopoietin for treating prolonged isolated thrombocytopenia after allogeneic stem cell transplantation.

机构信息

Peking University People's Hospital, Peking University Institute of Haematology, Beijing Key Laboratory of Haematopoietic Stem Cell Transplantation for the Treatment of Haematological Diseases , Beijing , P.R. China.

Peking-Tsinghua Centre for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University , Beijing , P.R. China.

出版信息

Platelets. 2019;30(8):994-1000. doi: 10.1080/09537104.2018.1557613. Epub 2018 Dec 20.

Abstract

Patients with prolonged isolated thrombocytopenia (PT) after allogeneic stem cell transplantation (allo-SCT) are known to have a poor prognosis. However, there is no standard treatment for PT. The present study aimed to investigate the potential effect of a novel recombinant human thrombopoietin (rhTPO) in a cohort of patients with PT following allo-SCT. A total of 24 patients with PT (including delayed platelet engraftment and secondary failure of platelet recovery) were treated with rhTPO from July 1, 2016 to May 31, 2017. rhTPO injections were administered at 300 IU/kg/d for 28 consecutive days or until platelet counts were ≥ 50 × 10/L, independent of platelet transfusion. Response was defined as platelet recovery to ≥ 20 × 10/L for seven consecutive days without transfusion support during or within 7 days of the end of rhTPO treatment. All patients completed the 28 days of treatment, and none were withdrawn due to adverse effects. The overall response was 45.8%, which was significantly higher than historical data (12.2%, < 0.001). The median response time was 12 (7-25) days from the initiation of rhTPO treatment. A response to rhTPO was associated with megakaryocytes in the bone marrow (positive vs. negative, 81.8 vs. 22.2%; p = 0.022). Among 11 patients exhibiting a response to rhTPO, the median number of megakaryocytes in bone marrow was increased significantly (10 vs. 2; = 0.036) after rhTPO treatment. In conclusion, the results of this preliminary study suggest that rhTPO may represent a therapeutic option, with a response of 45.8% for patients with PT after allo-SCT, and especially for those with megakaryocytes in the bone marrow. However, this should be further confirmed in randomized prospective clinical trials.

摘要

已知异基因造血干细胞移植(allo-SCT)后持续性孤立性血小板减少症(PT)的患者预后不良。然而,目前尚无 PT 的标准治疗方法。本研究旨在探讨新型重组人血小板生成素(rhTPO)在 allo-SCT 后 PT 患者中的潜在疗效。

2016 年 7 月 1 日至 2017 年 5 月 31 日,共有 24 例 PT 患者(包括血小板延迟植入和血小板恢复的继发性失败)接受 rhTPO 治疗。rhTPO 注射剂量为 300 IU/kg/d,连续 28 天,或直至血小板计数≥50×10/L,无需血小板输注。反应定义为在 rhTPO 治疗结束时或结束后 7 天内,无需输注支持,血小板恢复至≥20×10/L 且连续 7 天。所有患者均完成 28 天治疗,无因不良反应而退出。

总体反应率为 45.8%,明显高于历史数据(12.2%,<0.001)。rhTPO 治疗开始后,中位反应时间为 12(7-25)天。rhTPO 反应与骨髓中的巨核细胞有关(阳性 vs. 阴性,81.8% vs. 22.2%;p=0.022)。在 11 例对 rhTPO 有反应的患者中,rhTPO 治疗后骨髓中巨核细胞数量中位数显著增加(10 对 2;=0.036)。

综上所述,本初步研究结果表明,rhTPO 可能是一种治疗选择,allo-SCT 后 PT 患者的反应率为 45.8%,尤其是骨髓中有巨核细胞的患者。然而,这需要在随机前瞻性临床试验中进一步证实。

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