Suppr超能文献

一项多中心 2 期临床试验:地西他滨 10 天疗程、剂量递增供者淋巴细胞输注和鲁索替尼治疗异基因造血细胞移植后复发的急性髓系白血病和骨髓增生异常综合征。

A Multicenter Phase 2 Clinical Trial of 10-Day Decitabine, Dose-Escalated Donor Lymphocyte Infusion, and Ruxolitinib for Relapsed Acute Myeloid Leukemia and Myelodysplastic Syndromes after Allogeneic Hematopoietic Cell Transplantation.

机构信息

Division of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota, Minneapolis, Minnesota; Clinical Research Division, Fred Hutchinson Cancer Center and Division of Oncology, University of Washington, Seattle, Washington.

Division of Hematology and Oncology, University of Rochester, Rochester, New York.

出版信息

Transplant Cell Ther. 2023 May;29(5):328.e1-328.e6. doi: 10.1016/j.jtct.2023.02.010. Epub 2023 Feb 19.

Abstract

Post-transplantation relapse of acute myeloid leukemia and myelodysplastic syndromes has a poor prognosis. Donor lymphocyte infusion (DLI) is one treatment approach. However, efficacy is limited, and toxicity, mostly in the form of acute graft-versus-host disease (GVHD), is frequent. We tested a novel approach using 10-day decitabine, dose-escalated DLI, and ruxolitinib in a multicenter phase 2 trial aimed at increasing the efficacy of DLI and reducing its toxicity. Up to four 28-day cycles were administered. The primary endpoint was 6-month overall survival (OS). Of the 14 patients who started cycle 1, 13 received 1 DLI, 6 received 2 DLIs, and 1 received 3 4 DLIs. A preplanned interim analysis after enrolling 14 patients suggested futility, and the trial was closed to accrual. The final analysis showed a 6-month OS of 36% (95% confidence interval [CI], 18 to 72), a 1-year progression-free survival of 7% (95% CI, 1% to 47%), a 6-month cumulative incidence of grade II-IV acute GVHD of 57% (95% CI, 26% to 80%), and a 1-year nonrelapse mortality of 14% (95% CI, 2% to 38%). The combined modality treatment studied in this trial was ineffective and did not reduce DLI toxicity.

摘要

移植后急性髓系白血病和骨髓增生异常综合征的复发预后不良。供者淋巴细胞输注(DLI)是一种治疗方法。然而,疗效有限,且毒性频繁,主要表现为急性移植物抗宿主病(GVHD)。我们在一项多中心 2 期试验中测试了一种新方法,该方法使用 10 天的地西他滨、递增剂量的 DLI 和鲁索替尼,旨在提高 DLI 的疗效并降低其毒性。最多可进行四个 28 天的周期。主要终点是 6 个月总生存率(OS)。在开始第 1 周期的 14 名患者中,13 名接受了 1 次 DLI,6 名接受了 2 次 DLI,1 名接受了 3 次 4 次 DLI。在入组 14 名患者后进行的计划中期分析表明无效,试验停止入组。最终分析显示 6 个月 OS 为 36%(95%CI,18 至 72),1 年无进展生存率为 7%(95%CI,1%至 47%),6 个月 II 级至 IV 级急性 GVHD 的累积发生率为 57%(95%CI,26%至 80%),1 年非复发死亡率为 14%(95%CI,2%至 38%)。本试验中研究的联合治疗方法无效,并未降低 DLI 的毒性。

相似文献

引用本文的文献

本文引用的文献

8
Ruxolitinib for Glucocorticoid-Refractory Acute Graft-versus-Host Disease.
N Engl J Med. 2020 May 7;382(19):1800-1810. doi: 10.1056/NEJMoa1917635. Epub 2020 Apr 22.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验