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131I-抗 CD45 抗体联合氟达拉滨和低剂量全身照射预处理的异基因造血细胞移植治疗老年晚期急性髓系白血病或高危骨髓增生异常综合征患者。

Allogeneic hematopoietic cell transplantation after conditioning with 131I-anti-CD45 antibody plus fludarabine and low-dose total body irradiation for elderly patients with advanced acute myeloid leukemia or high-risk myelodysplastic syndrome.

机构信息

Division of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

出版信息

Blood. 2009 Dec 24;114(27):5444-53. doi: 10.1182/blood-2009-03-213298. Epub 2009 Sep 28.

DOI:10.1182/blood-2009-03-213298
PMID:19786617
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2798861/
Abstract

We conducted a study to estimate the maximum tolerated dose (MTD) of (131)I-anti-CD45 antibody (Ab; BC8) that can be combined with a standard reduced-intensity conditioning regimen before allogeneic hematopoietic cell transplantation. Fifty-eight patients older than 50 years with advanced acute myeloid leukemia (AML) or high-risk myelodysplastic syndrome (MDS) were treated with (131)I-BC8 Ab and fludarabine plus 2 Gy total body irradiation. Eighty-six percent of patients had AML or MDS with greater than 5% marrow blasts at the time of transplantation. Treatment produced a complete remission in all patients, and all had 100% donor-derived CD3(+) and CD33(+) cells in the blood by day 28 after the transplantation. The MTD of (131)I-BC8 Ab delivered to liver was estimated to be 24 Gy. Seven patients (12%) died of nonrelapse causes by day 100. The estimated probability of recurrent malignancy at 1 year is 40%, and the 1-year survival estimate is 41%. These results show that CD45-targeted radiotherapy can be safely combined with a reduced-intensity conditioning regimen to yield encouraging overall survival for older, high-risk patients with AML or MDS. This study was registered at www.clinicaltrials.gov as #NCT00008177.

摘要

我们进行了一项研究,旨在评估(131)I-抗 CD45 抗体(Ab;BC8)与标准的低强度预处理方案联合应用于异基因造血细胞移植前的最大耐受剂量(MTD)。58 例年龄大于 50 岁的晚期急性髓细胞白血病(AML)或高危骨髓增生异常综合征(MDS)患者接受了(131)I-BC8 Ab 联合氟达拉滨和 2 Gy 全身照射治疗。86%的患者在移植时骨髓原始细胞大于 5%。所有患者均获得完全缓解,且所有患者在移植后第 28 天血液中均有 100%的供体来源 CD3(+)和 CD33(+)细胞。(131)I-BC8 Ab 作用于肝脏的 MTD 估计为 24 Gy。7 例患者(12%)在 100 天内死于非复发原因。1 年时恶性肿瘤复发的估计概率为 40%,1 年生存率估计为 41%。这些结果表明,CD45 靶向放疗可以与低强度预处理方案安全联合,为年龄较大、AML 或 MDS 高危的患者带来令人鼓舞的总生存。该研究在 www.clinicaltrials.gov 上注册,编号为#NCT00008177。

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