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(90)替伊莫单抗 Y 与减低强度预处理及异基因造血干细胞移植治疗晚期滤泡性淋巴瘤。

(90)Y-ibritumomab tiuxetan followed by reduced-intensity conditioning and allo-SCT in patients with advanced follicular lymphoma.

机构信息

Lymphoma Program, Department of Medical Oncology, Harvard Medical School, Dana-Farber Cancer Institute, Boston, MA 02115-6084, USA.

出版信息

Bone Marrow Transplant. 2011 Dec;46(12):1503-9. doi: 10.1038/bmt.2010.339. Epub 2011 Jan 24.

Abstract

Reduced-intensity conditioning (RIC) hematopoietic SCT (HSCT) is a potentially curative therapeutic option for patients with advanced follicular lymphoma (FL), but disease relapse remains the most common cause of failure. Radioimmunoconjugates administered before RIC allo-HSCT may enhance cytoreduction and allow more time for GVL effect to develop without the associated toxicity of a myeloablative HSCT. We performed a retrospective study to describe the outcomes of patients with relapsed, refractory or transformed FL who received yttrium-90 ((90)Y)-ibritumomab tiuxetan followed by fludarabine and low-dose BU RIC allogeneic HSCT at the Dana-Farber Cancer Institute between 2006 and 2009, inclusively. Twelve patients were identified with a median age of 55 (40-66) years and a median number of lines of therapy of 5 (2-10). Two patients (17%) had transformed to a more aggressive histology and five (42%) had chemorefractory FL. Cumulative incidences of grade II-IV acute GVHD at 100 days were 17% (±11%) and chronic GVHD at 12 months were 63% (±19%). Two-year non-relapse mortality was 18% (±12%). Two-year OS and PFS were 83% (±11%) and 74% (±13%), respectively. This treatment is associated with favorable outcomes including acceptable rates of GVHD and relapse in advanced FL patients, and warrants prospective studies.

摘要

对于晚期滤泡性淋巴瘤 (FL) 患者,低强度预处理条件下的造血干细胞移植 (HSCT) 是一种潜在的治愈性治疗选择,但疾病复发仍然是最常见的失败原因。在低强度预处理异基因 HSCT 前给予放射性免疫偶联物可能会增强细胞减灭作用,并在没有清髓性 HSCT 相关毒性的情况下,为 GVL 效应的发展提供更多时间。我们进行了一项回顾性研究,以描述在 2006 年至 2009 年期间,在达纳-法伯癌症研究所接受钇-90 ((90)Y)-替伊莫单抗替昔坦联合氟达拉滨和低剂量 BU 低强度预处理异基因 HSCT 的复发性、难治性或转化性 FL 患者的结局。共确定了 12 名患者,中位年龄为 55 岁(40-66 岁),中位治疗线数为 5 条(2-10 条)。有 2 名患者(17%)转化为侵袭性更高的组织学类型,5 名患者(42%)对化疗有抗药性。100 天时 II-IV 级急性移植物抗宿主病的累积发生率为 17%(±11%),12 个月时慢性移植物抗宿主病的发生率为 63%(±19%)。2 年非复发死亡率为 18%(±12%)。2 年 OS 和 PFS 分别为 83%(±11%)和 74%(±13%)。这种治疗方法与晚期 FL 患者良好的结局相关,包括可接受的移植物抗宿主病和复发率,值得进一步开展前瞻性研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37f1/3139703/be04f7d33362/nihms256874f1.jpg

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