Medical Center, Department of Hematology & Oncology, University of Tuebingen, Tuebingen, Germany.
Blood. 2010 Sep 9;116(10):1795-802. doi: 10.1182/blood-2010-02-270538. Epub 2010 Jun 7.
Forty patients were enrolled in this phase 2 study combining radioimmunotherapy (RIT) using yttrium-90-ibritumomab-tiuxetan (15 MBq [0.4 mCi]/kg) with reduced-intensity conditioning (RIC) using fludarabine (90 mg/m(2)) and 2 Gy total body irradiation followed by allogeneic hematopoietic cell transplantation (HCT) from related (n = 13) or unrelated (n = 27) donors for the treatment of advanced non-Hodgkin lymphoma. Diagnoses were follicular lymphoma (n = 17), chronic lymphocytic leukemia (n = 13), mantle cell lymphoma (n = 8), marginal zone lymphoma (n = 1), and lymphoplasmacytic lymphoma (n = 1). Median age was 55 years (range, 34-68 years). All patients were high risk with refractory disease or relapse after preceding autologous HCT. No additional toxicities attributable to RIT were observed. Engraftment was rapid and sustained. Incidences of acute graft-versus-host disease 2-4 and chronic graft-versus-host disease were 43% and 53%, respectively. Kaplan-Meier-estimated nonrelapse mortality was 45% at 2 years. Twenty-two of 40 patients (55%) are alive, resulting in a Kaplan-Meier-estimated 2-year survival of 51% for all, 67% for follicular lymphoma, 49% for chronic lymphocytic leukemia, and 37% for mantle cell lymphoma patients. The combined use of RIT with RIC is feasible with acceptable toxicity, even in elderly and heavily pretreated patients. This study is registered at www.clinicaltrials.gov as #NCT00302757.
四十名患者参与了这项 2 期研究,该研究将放射性免疫治疗(RIT)与减少强度的预处理方案(RIC)相结合,RIC 方案采用氟达拉滨(90mg/m2)和 2Gy 全身照射,随后接受来自亲缘(n=13)或无关供者(n=27)的异基因造血细胞移植(HCT),以治疗晚期非霍奇金淋巴瘤。诊断为滤泡性淋巴瘤(n=17)、慢性淋巴细胞白血病(n=13)、套细胞淋巴瘤(n=8)、边缘区淋巴瘤(n=1)和淋巴浆细胞淋巴瘤(n=1)。中位年龄为 55 岁(范围,34-68 岁)。所有患者均为高危患者,伴有难治性疾病或在前次自体 HCT 后复发。未观察到与 RIT 相关的其他毒性。植入快速且持续。急性移植物抗宿主病 2-4 级和慢性移植物抗宿主病的发生率分别为 43%和 53%。2 年时非复发死亡率的 Kaplan-Meier 估计值为 45%。40 名患者中有 22 名(55%)存活,导致所有患者的 Kaplan-Meier 估计 2 年生存率为 51%,滤泡性淋巴瘤为 67%,慢性淋巴细胞白血病为 49%,套细胞淋巴瘤为 37%。RIT 与 RIC 的联合使用具有可行性,且毒性可接受,即使是在老年和大量预处理的患者中也是如此。这项研究在 www.clinicaltrials.gov 上注册,编号为 #NCT00302757。