Suppr超能文献

氟达拉滨/马法兰 100mg/m2 预处理联合异基因造血干细胞移植治疗成人噬血细胞性淋巴组织细胞增多症。

Fludarabine/Melphalan 100 mg/m Conditioning Therapy Followed by Allogeneic Hematopoietic Cell Transplantation for Adult Patients with Secondary Hemophagocytic Lymphohistiocytosis.

机构信息

Department of Hematology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

Department of Hematology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

出版信息

Biol Blood Marrow Transplant. 2019 Jun;25(6):1116-1121. doi: 10.1016/j.bbmt.2018.11.032. Epub 2018 Nov 30.

Abstract

Our previous research indicated that a reduced-intensity conditioning regimen (fludarabine and melphalan at 100 mg/m) was useful in allogeneic hematopoietic cell transplantation (HCT) for patients with lymphoma. This retrospective study evaluated the reduced-intensity conditioning regimen in allogeneic HCT for adult patients with hemophagocytic lymphohistiocytosis (HLH). Sixteen patients with HLH were evaluated, including 6 patients who were enrolled in a prospective clinical trial (NCT00772811) and 10 patients who received the same conditioning regimen (fludarabine at 30 mg/m/day on days -6 to -2 and melphalan at 100 mg/m on day -2). The median age was 42 years (range, 18 to 64), and 12 patients had Epstein-Barr virus (EBV)-associated HLH. Donors were an HLA matched sibling for 10 patients, an unrelated matched volunteer for 4 patients, and a mismatched family member for 2 patients. After excluding 3 patients who died soon after HCT, 12 patients achieved an engraftment (neutrophil median, day 12; platelet median, day 16). Five patients experienced acute graft-versus-host disease (GVHD), including 1 case of grade II and 4 cases of grades III to IV. Chronic GVHD occurred in 3 patients (moderate, 1 case; severe, 2 cases). After a median follow-up of 33.8 months 1 patient progressed, 3 patients relapsed, and 9 patients died. Five deaths were unrelated to relapse or progression and were caused by infection (n = 3), bleeding (n = 1), and GVHD (n = 1). No deaths or relapses were observed at >124 days post-transplant. The overall survival rate was 48.6%, and significant differences were observed according to pretransplant ferritin level (P = .007) and cytopenia lineage (P = .021). Before allogeneic HCT 10 of 12 patients still tested positive for EBV DNA: 6 patients tested negative for EBV DNA after HCT, 2 patients had persistent EBV DNA, and 2 patients were unassessable because of early death. Conditioning therapy using a lower dose of melphalan combined with fludarabine appears to be promising in allogeneic HCT for adults with HLH. However, strategies are needed to reduce the risk of early death.

摘要

我们之前的研究表明,对于淋巴瘤患者,采用减低强度预处理方案(氟达拉滨和马法兰,剂量为 100mg/m2)进行异基因造血细胞移植(HCT)是有效的。这项回顾性研究评估了减低强度预处理方案在成人噬血细胞性淋巴组织细胞增多症(HLH)患者异基因 HCT 中的应用。共评估了 16 例 HLH 患者,包括 6 例入组前瞻性临床试验(NCT00772811)的患者和 10 例接受相同预处理方案(氟达拉滨 30mg/m2/天,于-6 至-2 天给予;马法兰 100mg/m2 于-2 天给予)的患者。中位年龄为 42 岁(范围 18 至 64 岁),12 例患者为 EBV 相关 HLH。供者为 10 例患者的 HLA 匹配同胞、4 例无关匹配志愿者和 2 例不匹配的家庭成员。排除 3 例 HCT 后短期内死亡的患者后,12 例患者获得了植入(中性粒细胞中位时间为 12 天;血小板中位时间为 16 天)。5 例患者发生急性移植物抗宿主病(GVHD),包括 1 例 2 级和 4 例 3 至 4 级。3 例患者发生慢性 GVHD(中度 1 例;重度 2 例)。中位随访 33.8 个月后,1 例患者进展,3 例患者复发,9 例患者死亡。5 例死亡与复发或进展无关,分别由感染(n=3)、出血(n=1)和 GVHD(n=1)导致。移植后>124 天未观察到死亡或复发。总体生存率为 48.6%,根据移植前铁蛋白水平(P=.007)和细胞减少谱系(P=.021)观察到显著差异。在异基因 HCT 前,12 例患者中有 10 例仍检测到 EBV DNA 阳性:6 例患者 HCT 后 EBV DNA 转为阴性,2 例患者持续存在 EBV DNA,2 例患者因早期死亡而无法评估。使用较低剂量马法兰联合氟达拉滨的预处理方案似乎在成人 HLH 患者的异基因 HCT 中很有前景。然而,需要制定策略来降低早期死亡的风险。

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