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首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Phase I Study of Clofarabine and 2-Gy Total Body Irradiation as a Nonmyeloablative Preparative Regimen for Hematopoietic Stem Cell Transplantation in Pediatric Patients with Hematologic Malignancies: A Therapeutic Advances in Childhood Leukemia Consortium Study
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Phase I Study of Clofarabine and 2-Gy Total Body Irradiation as a Nonmyeloablative Preparative Regimen for Hematopoietic Stem Cell Transplantation in Pediatric Patients with Hematologic Malignancies: A Therapeutic Advances in Childhood Leukemia Consortium Study

机译:I阶段研究Clofarabine和2-Gy总体辐照作为血液学恶性肿瘤儿科患者造血干细胞移植中的非植物干细胞移植方案:儿童白血病联盟研究的治疗进展

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Clofarabine is a purine nucleoside analog with immunosuppressive and antileukemic activity and its inclusion in reduced-intensity regimens could potentially improve outcomes. We performed a prospective phase I study of clofarabine combined with 2 Gy total body irradiation (TBI) as a nonmyeloablative preparative regimen for allogeneic stem cell transplantation in pediatric patients who were considered at high risk of mortality from standard myeloablative regimens. The main goal of the study was to delineate the maximum feasible dose (MFD) of clofarabine in combination with 2 Gy TBI. Eighteen patients, 1 to 21 years of age and in complete remission, were enrolled in 2 strata (matched related donor and unrelated donor) and evaluated for day100 dose-limiting events (DLE) (nonengraftment, nonrelapse mortality [NRM], and severe renal insufficiency) after receiving clofarabine at the starting dose level of 40 mg/m(2). All 6 patients (3 in each stratum) engrafted with no day 100 DLE seen in the first cohort. The dose was increased to 52 mg/m2 in the next and an expanded cohort (total of 12 patients) and no DLE were observed at day 100 and at the 1-year study endpoint. The regimen was well tolerated with transient transaminitis and gastrointestinal and skin reactions as the common reversible toxicities observed with clofarabine. The dose of 52 mg/m2 of clofarabine was deemed the MFD. Disease relapse led to mortality in 6 (33%) patients during follow-up with 1-year event-free survival and overall survival of 60% (95% confidence interval [CI], 34 to 79) and 71% (95% CI, 44 to 87), respectively. This regimen leads to successful engraftment using both related and unrelated donors with exceptionally low rates of NRM. (C) 2017 American Society for Blood and Marrow Transplantation.
机译:Clofarabine是一种嘌呤核苷与免疫抑制和抗血清血症活性的类似物,并且其在减少强度方案中的包含可能会改善结果。我们进行了一项预期阶段,我研究了氯氟沙明酸的研究与2 Gy全身照射(TBI)相结合,作为异构性干细胞移植在儿科患者中的非茂剂制剂方案,该儿科患者从标准的米洛匹米方案中被考虑的死亡率高。该研究的主要目标是将氯氟沙滨的最大可行剂量(MFD)与2 Gy TBI联合制定。 18名患者,1至21岁,完全缓解,注册了2个层次(匹配的相关供体和不相关的供体),并评估了DAY100剂量限制事件(DLE)(非原营,非筛选死亡率[NRM]和严重肾脏在从40mg / m(2)的起始剂量水平接受柠檬酰滨后,不足)。所有6名患者(每个地层3例)植入了第一个队列中没有一天100个DLE。在下一个和扩张的群组中,剂量增加到52mg / m 2,并且在第100天和1年的研究终点中没有观察到DLE。该方案具有良好的曲敏炎和胃肠和皮肤反应,作为氯氟沙滨观察到的常见可逆毒性。 52mg / m 2的氯苯胺的剂量被认为是MFD。疾病复发导致6名(33%)患者的死亡率,在随访期间,无需1年的无事项存活和60%(95%置信区间[CI],34至79)和71%(95%CI)的总生存率44至87)分别。该方案使用既有相关和无关的捐献者都会导致成功的植入,不相关的捐献者具有异常低的NRM率。 (c)2017年美国血液和骨髓移植协会。

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