首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Fludarabine-based reduced intensity conditioning for stem cell transplantation of Fanconi anemia patients from fully matched related and unrelated donors.
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Fludarabine-based reduced intensity conditioning for stem cell transplantation of Fanconi anemia patients from fully matched related and unrelated donors.

机译:基于氟达拉滨的降低强度调节,用于来自完全匹配的相关和不相关供体的Fanconi贫血患者的干细胞移植。

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摘要

Reduced intensity conditioning has been suggested as a desirable therapeutic modality for the treatment of patients with malignant and nonmalignant indications, but it seems particularly attractive for patients with Fanconi anemia due to their increased sensitivity to chemoradiotherapy. Between November 1996 and September 2003, 7 patients (1 male and 6 female; age range, 3-31 years; median age, 9.5) were conditioned with a fludarabine-based protocol for stem cell transplantation without radiation. In vivo T-cell depletion was accomplished with anti-thymocytic globulin or Campath-1H (alemtuzumab). Graft-versus-host disease prophylaxis consisted of low-dose cyclosporine alone. Eight transplantations were carried out for 7 patients using bone marrow, peripheral blood, and/or cord blood as sources of stem cells. All patients received transplants from HLA-A, -B, -C, and -DR matched donors, 5 from family members and 2 from matched unrelated donors. One patient did not engraft her first matched unrelated donor and underwent a second transplantation from another matched unrelated donor, after which she engrafted well. All 7 patients are alive and well, fully reconstituted with donor cells, and with 100% performance status. In conclusion, fludarabine-based preparative protocols are well tolerated, facilitate rapid engraftment with minimal toxicity, and should be considered an essential component of choice for patients with Fanconi anemia.
机译:强度降低的调理已被建议作为治疗恶性和非恶性适应症患者的理想治疗方式,但是对于Fanconi贫血患者而言,由于其对放化疗的敏感性增加,似乎特别有吸引力。在1996年11月至2003年9月之间,对7例患者(1例男性和6例女性;年龄范围为3-31岁;中位年龄为9.5岁)进行了基于氟达拉滨的无辐射干细胞移植治疗。用抗胸腺细胞球蛋白或Campath-1H(alemtuzumab)完成体内T细胞清除。预防移植物抗宿主病仅由低剂量环孢霉素组成。使用骨髓,外周血和/或脐带血作为干细胞来源,对7位患者进行了八次移植。所有患者均接受了HLA-A,-B,-C和-DR匹配供体的移植,其中5位来自家庭成员,2位来自相配的无关亲戚。一位患者没有移植她的第一个匹配的无关供者,并从另一位匹配的无关的捐赠者进行了第二次移植,之后她很好地移植了。所有7例患者都活得很好,并完全恢复了供体细胞的状态,并且表现为100%。总之,基于氟达拉滨的制备方案耐受性良好,有利于快速植入,且毒性极小,应被视为范可尼贫血患者选择的必不可少的组成部分。

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