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移植预处理期使用芦可替尼可预防骨髓纤维化患者异基因造血干细胞移植后发生急性移植物抗宿主病。

Peritransplantation Ruxolitinib Prevents Acute Graft-versus-Host Disease in Patients with Myelofibrosis Undergoing Allogenic Stem Cell Transplantation.

机构信息

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

Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; Department of Haematology, Ampang Hospital, Selangor, Malaysia.

出版信息

Biol Blood Marrow Transplant. 2018 Oct;24(10):2152-2156. doi: 10.1016/j.bbmt.2018.05.023. Epub 2018 May 22.

Abstract

JAK inhibition by ruxolitinib is approved for treating myelofibrosis and also has shown efficacy in treating steroid-resistant acute and chronic graft-versus-host disease (GVHD). In 12 patients with myelofibrosis (median age, 63 years; range, 43 to 71 years) who were treated with ruxolitinib and underwent allogeneic stem cell transplantation (ASCT), ruxolitinib was continued (2 × 5 mg daily) until stable engraftment. No graft failure was observed, and leukocyte engraftment was achieved after a median of 12 days (range, 11 to 18 days). One patient developed fever of unknown origin after discontinuation of ruxolitinib; otherwise, no withdrawal syndrome was observed. Overall, only 1 patient each experienced acute GVHD grade I or II, resulting in an 8% incidence of acute GVHD grade II-IV at day +100, with no nonrelapse mortality. Complete chimerism was achieved in 11 patients after a median of 40 days, and molecular clearance of the underlying driver mutation was noted in 10 patients after a median of 32 days. Cytomegalovirus (CMV) reactivation occurred in 5 patients (41%), 1 of whom had CMV colitis as well, but all resolved after ganciclovir treatment. In 2 patients, ruxolitinib had to be discontinued on day 17 and day 18 after ASCT due to cytopenia after engraftment. Levels of inflammatory cytokines IL-8, IL-10, IL-6, TNFR2, INF-α, and INF-β were reduced after ruxolitinib treatment. After day +100, 4 patients developed acute GVHD (1 with grade I, 2 with grade II, and 1 with grade III) after tapering of cyclosporine, and all patients were alive at a median follow-up of 17 months (range, 12 to 18 months).

摘要

芦可替尼通过抑制 JAK 治疗骨髓纤维化,也已显示出治疗激素耐药性急性和慢性移植物抗宿主病(GVHD)的疗效。在 12 例接受芦可替尼治疗且接受异基因干细胞移植(ASCT)的骨髓纤维化患者(中位年龄 63 岁;范围 43 至 71 岁)中,在稳定植入后继续使用芦可替尼(每天 2×5mg)。未观察到移植物衰竭,白细胞植入中位数为 12 天(范围 11 至 18 天)。1 例患者在停用芦可替尼后出现不明原因发热;否则,未观察到停药综合征。总体而言,仅有 1 例患者分别发生 1 级或 2 级急性 GVHD,导致第 100 天急性 GVHD 2 级至 4 级的发生率为 8%,无非复发死亡率。11 例患者在中位 40 天后获得完全嵌合,10 例患者在中位 32 天后检测到潜在驱动突变的分子清除。5 例(41%)患者发生巨细胞病毒(CMV)再激活,其中 1 例还伴有 CMV 结肠炎,但所有患者在接受更昔洛韦治疗后均得到解决。在 2 例患者中,在 ASCT 后第 17 天和第 18 天,由于植入后细胞减少,芦可替尼不得不停药。芦可替尼治疗后,白细胞介素 8(IL-8)、白细胞介素 10(IL-10)、白细胞介素 6(IL-6)、肿瘤坏死因子受体 2(TNFR2)、干扰素-α(INF-α)和干扰素-β(INF-β)的炎症细胞因子水平降低。在第 100 天之后,在环孢素减量后,4 例患者出现急性 GVHD(1 例为 1 级,2 例为 2 级,1 例为 3 级),所有患者在中位随访 17 个月(范围 12 至 18 个月)时均存活。

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