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芦可替尼早期给药可降低急性白血病异基因造血干细胞移植后急性移植物抗宿主病。

Ruxolitinib early administration reduces acute GVHD after alternative donor hematopoietic stem cell transplantation in acute leukemia.

机构信息

Department of Hematology, Affiliated Cancer Hospital of Zhengzhou University and Henan Cancer Hospital, Zhengzhou, 450000, Henan, China.

Henan Academy of Medical and Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450000, Henan, China.

出版信息

Sci Rep. 2021 Apr 19;11(1):8501. doi: 10.1038/s41598-021-88080-3.

Abstract

This study aimed to observe the safety and clinical efficacy of early application of ruxolitinib to prevent acute graft-versus-host disease (aGVHD) after alternative donor transplantation in acute leukemia. There were 57 patients undergoing allo-HSCT at the Affiliated Cancer Hospital of Zhengzhou University from July 2017 to October 2019. They were divided into control(16 patients) and ruxolitinib (41 patients) groups. For aGVHD prophylaxis, the control group received post-transplantation cyclophosphamide, antithymocyte globulin-Fresenius, cyclosporine A, and mycophenolate mofetil, while in the ruxolitinib group, ruxolitinib 5 mg/d in adults or 0.07-0.1 mg/(kg d) in children was administered from the day of neutrophil engraftment to 100 days post-transplantation based on control group. We found 55 patients had successful reconstitution of hematopoiesis; No significant difference was found in cGVHD, hemorrhagic cystitis, pulmonary infection, intestinal infection, Epstein-Barr virus infection, cytomegalovirus infection, relapse, death, and nonrelapse mortality. The incidences of aGVHD (50 vs. 22%, P = 0.046) and grade II-IV aGVHD (42.9 vs. 12.2%, P = 0.013) were significantly higher in the control group than in the ruxolitinib group. No significant differences were observed in overall survival (P = 0.514), disease-free survival (P = 0.691), and cumulative platelet transfusion within 100 days post-transplantation between two groups. This suggests early application of ruxolitinib can reduce the incidence and severity of aGVHD and patients are well tolerated.

摘要

本研究旨在观察早期应用鲁索利替尼预防急性白血病异基因造血干细胞移植后急性移植物抗宿主病(aGVHD)的安全性和临床疗效。2017 年 7 月至 2019 年 10 月,郑州大学附属肿瘤医院共收治 57 例接受allo-HSCT 的患者,分为对照组(16 例)和鲁索利替尼组(41 例)。对于 aGVHD 的预防,对照组患者接受移植后环磷酰胺、抗胸腺细胞球蛋白-Fresenius、环孢素 A 和吗替麦考酚酯治疗,而在鲁索利替尼组中,从中性粒细胞植入之日起至移植后 100 天,给予成人 5mg/d 或儿童 0.07-0.1mg/(kg·d)的鲁索利替尼。我们发现 55 例患者造血重建成功;两组间 cGVHD、出血性膀胱炎、肺部感染、肠道感染、EB 病毒感染、巨细胞病毒感染、复发、死亡和非复发死亡率无显著差异。对照组 aGVHD(50%比 22%,P=0.046)和 II-IV 级 aGVHD(42.9%比 12.2%,P=0.013)的发生率明显高于鲁索利替尼组。两组患者的总生存率(P=0.514)、无病生存率(P=0.691)和移植后 100 天内血小板输注总量无显著差异。这表明早期应用鲁索利替尼可降低 aGVHD 的发生率和严重程度,且患者耐受良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c72/8055912/cad099af420d/41598_2021_88080_Fig1_HTML.jpg

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