首页> 外文期刊>Bone marrow transplantation >A fludarabine, thiotepa reduced toxicity conditioning regimen designed specifically for allogeneic second haematopoietic cell transplantation after failure of previous autologous or allogeneic transplantation.
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A fludarabine, thiotepa reduced toxicity conditioning regimen designed specifically for allogeneic second haematopoietic cell transplantation after failure of previous autologous or allogeneic transplantation.

机译:氟达拉滨,噻替帕减少毒性的调理方案,专为先前的自体或异体移植失败后的异体第二次造血细胞移植而设计。

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摘要

We present a phase II study of fludarabine 5 x 30 mg/m(2), thiotepa 3 x 5 mg/kg as preparative regimen specifically for allogeneic second haematopoietic stem cell transplantation (HCT) after failure of previous HCT. Forty-nine patients (median age 52 years, range 27-68) received an allogeneic second HCT after failed autologous (n=29) or allogeneic (n=20) HCT. Diagnoses were AML (n=18), ALL (n=3), multiple myeloma (n=11), lymphoma (n=16) and CML (n=1). GVHD prophylaxis consisted of CYA and mainly low dose alemtuzumab (40 mg). The median follow-up for patients alive is 528 days (range 217-1344). In 43 of 49 (88%) evaluable patients response rates were CR=19, PR=14 and SD=10 at one month. At one year, the probability (95% confidence interval) of relapse is 55.1 (38.2-72)% and the nonrelapse mortality (NRM) is 29 (14.2-44.4)%. Estimated survival at one year is 42.6 (28.7-56.6)% and event free survival is 38.1 (24.4-51.8)%. Survival was significantly better for patients experiencing relapse beyond one year,than for patients relapsing within one year from first transplantation (51.2 (33.5-68.9)% vs 27 (7-48.5)%; P=0.013). We conclude that this regimen is feasible and well tolerated for allogeneic second HCT.
机译:我们提出氟达拉滨5 x 30 mg / m(2),噻替帕3 x 5 mg / kg作为准备方案的II期研究,该方案​​专门用于先前HCT失败后的同种异体第二代造血干细胞移植(HCT)。四十九例患者(中位年龄52岁,范围27-68)在自体(n = 29)或异体(n = 20)HCT失败后接受了异基因第二次HCT。诊断为AML(n = 18),ALL(n = 3),多发性骨髓瘤(n = 11),淋巴瘤(n = 16)和CML(n = 1)。预防GVHD包括CYA和主要是小剂量的Alemtuzumab(40 mg)。存活患者的中位随访时间为528天(范围217-1344)。 49例患者中有43例(88%)可评估的患者一个月的缓解率为CR = 19,PR = 14和SD = 10。一年后,复发的可能性(95%置信区间)为55.1(38.2-72)%,非复发死亡率(NRM)为29(14.2-44.4)%。一年的估计生存率为42.6(28.7-56.6)%,无事件生存率为38.1(24.4-51.8)%。一年以上复发的患者的生存期明显优于首次移植后一年内复发的患者(51.2(33.5-68.9)%vs 27(7-48.5)%; P = 0.013)。我们得出结论,对于同种异体第二HCT,该方案是可行的且耐受性良好。

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