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一项关于克拉屈滨联合大剂量马法兰作为异基因移植的降低强度预处理方案在成人中的 I 期研究。

A phase I study in adults of clofarabine combined with high-dose melphalan as reduced-intensity conditioning for allogeneic transplantation.

机构信息

Department of Hematology/Hematopoietic Cell Transplantation, City of Hope, Duarte, California 91010, USA.

出版信息

Biol Blood Marrow Transplant. 2012 Mar;18(3):432-40. doi: 10.1016/j.bbmt.2011.07.017. Epub 2011 Jul 27.

Abstract

Clofarabine is a novel purine nucleoside analog with immunosuppressive and antileukemia activity. We performed a phase I study of the combination of clofarabine plus melphalan as a reduced-intensity conditioning regimen for allogeneic stem cell transplantation in patients with acute myelogenous leukemia. Patients over age 18 in complete remission or with active disease (up to 50% marrow blasts) who had a matched related or unrelated donor were eligible. The conditioning regimen consisted of escalating doses of clofarabine plus melphalan, followed by allogeneic stem cell transplantation. Sixteen patients (median age, 63 years) were treated at 3 dose levels; 4 of these patients had primary induction failure, and 3 were in first relapse. One patient at dose level 2 and 1 patient at dose level 3 died of multiorgan toxicity; no other dose-limiting toxicities were seen. All other patients at both doses of clofarabine studied demonstrated complete engraftment by day 30, with a median time to absolute neutrophil count recovery of 14 days, and 16 days for platelet recovery. With a median follow-up of 17 months, only 2 patients relapsed, and 4 patients died. Clofarabine plus melphalan at dose level 2 is a well-tolerated conditioning regimen with activity in patients with advanced acute myelogenous leukemia.

摘要

克氯法拉滨是一种新型嘌呤核苷类似物,具有免疫抑制和抗白血病活性。我们进行了一项Ⅰ期研究,评估克氯法拉滨联合马法兰作为异基因造血干细胞移植预处理方案在急性髓细胞白血病患者中的应用。完全缓解或有活动疾病(最多 50%骨髓原始细胞)、有匹配的相关或无关供者的 18 岁以上患者符合入组条件。预处理方案包括递增剂量的克氯法拉滨联合马法兰,随后进行异基因造血干细胞移植。16 例患者(中位年龄 63 岁)接受了 3 个剂量水平的治疗;其中 4 例患者存在原发性诱导失败,3 例患者处于首次复发。1 例患者在剂量水平 2,1 例患者在剂量水平 3 死于多器官毒性;未观察到其他剂量限制性毒性。在研究的克氯法拉滨两个剂量水平中,所有其他患者均在第 30 天完全植入,中性粒细胞绝对计数恢复的中位时间为 14 天,血小板恢复的中位时间为 16 天。中位随访 17 个月时,仅 2 例患者复发,4 例患者死亡。克氯法拉滨联合马法兰在剂量水平 2 时耐受性良好,在晚期急性髓细胞白血病患者中具有活性。

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