Suppr超能文献

异基因造血干细胞移植后使用鲁索替尼维持治疗时慢性移植物抗宿主病的发生率较低。

Low rates of chronic graft-versus-host disease with ruxolitinib maintenance following allogeneic HCT.

作者信息

DeFilipp Zachariah, Kim Haesook T, Knight Laura W, O'Connor Suzanne M, Dhaver Shilton E, White Meghan, Dholaria Bhagirathbhai, Schroeder Mark A, Vasu Sumithira, Abedin Sameem, Chung Jooho, El-Jawahri Areej, Frigault Matthew J, McAfee Steven, Newcomb Richard A, O'Donnell Paul V, Spitzer Thomas R, Chen Yi-Bin, Hobbs Gabriela S

机构信息

Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.

Department of Data Science, Dana-Farber Cancer Institute and Harvard T.H. Chan School of Public Health, Boston, MA.

出版信息

Blood. 2025 May 15;145(20):2312-2316. doi: 10.1182/blood.2024028005.

Abstract

Despite recent advances in graft-versus-host disease (GVHD) prophylaxis, novel approaches to effective prevention of chronic GVHD (cGVHD) remain of high importance. In this prospective, multicenter, phase 2 trial, ruxolitinib, an oral inhibitor of Janus kinase (JAK) 1 and 2, was administered as maintenance therapy after reduced-intensity allogeneic hematopoietic cell transplantation (HCT). GVHD prophylaxis consisted of tacrolimus and methotrexate. Ruxolitinib began between day +30 to 100 and was administered continuously in 28-day cycles for up to 24 cycles. Seventy-eight participants were enrolled before HCT; 63 participants received the intervention. The median start date of ruxolitinib after HCT was day +45. The most common grade ≥3 adverse events were neutropenia, thrombocytopenia, and anemia. Seven participants experienced grade ≥3 infectious events. GVHD-free, relapse-free survival at 1 year after HCT, the primary end point, was 70%. Grade 3 to 4 acute GVHD at 6 months was 4.8%, and moderate-severe cGVHD at 2 years was 16%. cGVHD requiring systemic therapy was 9.5% at 1 year and 13% at 2 years. Overall survival and progression-free survival at 2 years were 76% and 68%, respectively. Prolonged administration of ruxolitinib following HCT is associated with low rates of clinically significant cGVHD. The incorporation of JAK inhibition into GVHD prevention approaches warrants further investigation. This trial was registered at www.clinicaltrials.gov as #NCT03286530.

摘要

尽管在移植物抗宿主病(GVHD)预防方面取得了最新进展,但有效预防慢性GVHD(cGVHD)的新方法仍然至关重要。在这项前瞻性、多中心、2期试验中,鲁索替尼(一种Janus激酶(JAK)1和2的口服抑制剂)在降低强度的异基因造血细胞移植(HCT)后作为维持治疗给药。GVHD预防包括他克莫司和甲氨蝶呤。鲁索替尼在第30至100天开始给药,以28天为周期持续给药,最多24个周期。78名参与者在HCT前入组;63名参与者接受了干预。HCT后鲁索替尼的中位开始日期为第45天。最常见的≥3级不良事件是中性粒细胞减少、血小板减少和贫血。7名参与者经历了≥3级感染事件。HCT后1年的无GVHD、无复发生存率(主要终点)为70%。6个月时3至4级急性GVHD为4.8%,2年时中度至重度cGVHD为16%。需要全身治疗的cGVHD在1年时为9.5%,在2年时为13%。2年时的总生存率和无进展生存率分别为76%和68%。HCT后长期服用鲁索替尼与临床上显著的cGVHD发生率低有关。将JAK抑制纳入GVHD预防方法值得进一步研究。该试验在www.clinicaltrials.gov上注册为#NCT03286530。

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