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泼尼松和依维莫司治疗新诊断的中度或重度慢性移植物抗宿主病(PredEver 研究):一项前瞻性多中心 IIA 期研究。

Treatment of newly diagnosed moderate or severe chronic graft-versus-host disease with prednisone and everolimus (PredEver first): a prospective multicenter phase IIA study.

机构信息

Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Department of Hematology, Medical Oncology, and Pneumology, University Medical Center, Mainz, Germany.

出版信息

Bone Marrow Transplant. 2024 Aug;59(8):1092-1096. doi: 10.1038/s41409-024-02289-0. Epub 2024 May 2.

Abstract

Although most patients with chronic graft-versus-host disease (cGVHD) show initial response to first-line therapy, long-term clinically meaningful success of first-line treatment remains rare. In a prospective multicentre phase II trial in 6 German centers, patients with newly diagnosed moderate or severe cGVHD received prednisone and everolimus for 12 months followed by a 1-year follow-up period. Primary endpoint was treatment success (TS) at 6 months defined as patient being alive, achieving PR or CR of cGVHD, having no relapse of underlying disease and requiring no secondary treatment for cGVHD. Of the 34 patients evaluable for efficacy, 19 (56%) had TS at 6 months with 22 and 52% of the patients in a CR and PR respectively. Overall 30 patients (88%) had a CR or PR as best response, nearly all responses (29/30) occurring within the first 6 weeks of treatment. The cumulative incidence of treatment failure at 1 year was 63%, corresponding to 37% TS. Predefined safety endpoint (thrombotic microangiopathy, pneumonitis, and avascular necrosis) were not observed in any patient. Addition of everolimus to prednisolone is well tolerated and may improve long-term treatment success. Larger studies are necessary to ascertain the possible role of everolimus in first-line treatment of cGVHD.

摘要

尽管大多数慢性移植物抗宿主病 (cGVHD) 患者对一线治疗有初始反应,但一线治疗长期获得有临床意义的成功仍然很少见。在 6 家德国中心进行的一项前瞻性多中心 II 期试验中,新诊断为中重度 cGVHD 的患者接受泼尼松和依维莫司治疗 12 个月,随后进行 1 年的随访期。主要终点是 6 个月时的治疗成功 (TS),定义为患者存活、cGVHD 达到 PR 或 CR、无基础疾病复发且无需 cGVHD 二级治疗。在可评估疗效的 34 例患者中,19 例 (56%) 在 6 个月时达到 TS,分别有 22%和 52%的患者达到 CR 和 PR。总体而言,30 例患者 (88%) 获得了 CR 或 PR 作为最佳反应,几乎所有反应 (29/30) 均发生在治疗的前 6 周内。1 年后治疗失败的累积发生率为 63%,对应 TS 为 37%。未观察到任何患者出现预定的安全性终点 (血栓性微血管病、肺炎和骨坏死)。依维莫司联合泼尼松龙耐受性良好,可能提高长期治疗成功率。需要更大规模的研究来确定依维莫司在 cGVHD 一线治疗中的可能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b295/11296949/e18be33902b5/41409_2024_2289_Fig1_HTML.jpg

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