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采用移植后环磷酰胺的低毒性替代供体干细胞移植治疗原发性免疫缺陷病。

Reduced-toxicity alternate-donor stem cell transplantation with posttransplant cyclophosphamide for primary immunodeficiency disorders.

作者信息

Rastogi Neha, Katewa Satyendra, Thakkar Dhwanee, Kohli Shruti, Nivargi Sagar, Yadav Satya Prakash

机构信息

Pediatric Hematology Oncology Unit, Department of Pediatrics, Fortis Memorial Research Institute, Gurgaon, Haryana, India.

Department of Pediatric Hematology Oncology & BMT, Medanta The Medicity Hospital, Gurgaon, Haryana, India.

出版信息

Pediatr Blood Cancer. 2018 Jan;65(1). doi: 10.1002/pbc.26783. Epub 2017 Sep 13.

Abstract

We describe here the outcomes of reduced-toxicity alternate-donor stem cell transplant (SCT) with posttransplant cyclophosphamide (PTCy) for primary immunodeficiency disorders (PIDs) in eight children (haploidentical-seven and matched unrelated donor-one). The conditioning was with serotherapy (alemtuzumab-3/rabbit-anti-thymoglobulin-5); fludarabine, cyclophosphamide, and total body irradiation-5 (additional thiotepa-3); fludarabine and treosulfan-2; and fludarabine and busulfan-1. All received PTCy 50 mg/kg on days 3 and 4 as graft versus host disease prophylaxis along with tacrolimus and mycophenolate. Mean CD34 dose was 13.8 × 10 /kg. Two children died because of PIDs. Acute graft versus host disease up to grades I and II was seen in three children. All six survivors are fully donor and disease free at median follow-up of 753 days. Alternate donor SCT with PTCy is feasible in PID and has good outcomes.

摘要

我们在此描述了采用移植后环磷酰胺(PTCy)进行低毒性替代供体干细胞移植(SCT)治疗8例儿童原发性免疫缺陷病(PID)的结果(单倍体相合供体7例,匹配的无关供体1例)。预处理方案包括:血清疗法(阿仑单抗3例/兔抗胸腺细胞球蛋白5例);氟达拉滨、环磷酰胺及全身照射5例(另外3例加用噻替派);氟达拉滨和曲奥舒凡2例;氟达拉滨和白消安1例。所有患儿在第3天和第4天均接受50mg/kg的PTCy以预防移植物抗宿主病,同时使用他克莫司和霉酚酸酯。平均CD34剂量为13.8×10⁶/kg。2例儿童因PID死亡。3例儿童出现了I级和II级急性移植物抗宿主病。在中位随访753天时,所有6例存活者均完全为供体来源且无疾病。采用PTCy的替代供体SCT在PID治疗中是可行的,且效果良好。

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