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CXCR4 导向放射性配体疗法治疗晚期弥漫性大 B 细胞淋巴瘤的可行性。

Feasibility of CXCR4-Directed Radioligand Therapy in Advanced Diffuse Large B-Cell Lymphoma.

机构信息

Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany

Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany.

出版信息

J Nucl Med. 2019 Jan;60(1):60-64. doi: 10.2967/jnumed.118.210997. Epub 2018 May 18.

Abstract

We have recently reported on our experience with C-X-C-motif chemokine receptor 4 (CXCR4)-directed radioligand therapy (RLT) in multiple myeloma and acute leukemia. Six patients with heavily pretreated relapsed diffuse large B-cell lymphoma (3 men, 3 women; aged, 54 ± 8 y) underwent CXCR4-directed RLT in combination with conditioning chemotherapy and allogeneic stem cell transplantation. In 2 patients, radioimmunotherapy targeting CD20 or CD66 was added to enhance antilymphoma activity. Endpoints were incidence and severity of adverse events, progression-free survival, and overall survival. RLT and additional radioimmunotherapy were well tolerated, without any acute adverse events or changes in vital signs. Successful engraftment was recorded after a median of 11 d (range, 9-13 d). Of the 4 patients who were available for follow-up (one patient died of CNS aspergillosis 29 d after RLT and another of sepsis in aplasia 34 d after RLT), CXCR4-directed RLT resulted in a partial response in two (both treated with additional radioimmunotherapy) and a mixed response in the remaining two. The response duration was rather short-lived, with a median progression-free survival of 62 d (range, 29-110 d) and a median overall survival of 76 d (range, 29-334 d). CXCR4-directed RLT (in combination with additional radioimmunotherapy) is feasible as a conditioning regimen before allogeneic stem cell transplantation in diffuse large B-cell lymphoma.

摘要

我们最近报道了我们在多发性骨髓瘤和急性白血病中使用 C-X-C 基序趋化因子受体 4(CXCR4)导向放射性配体疗法(RLT)的经验。6 例接受过大量预处理的复发性弥漫性大 B 细胞淋巴瘤(3 名男性,3 名女性;年龄,54±8 岁)患者接受了 CXCR4 导向的 RLT 联合预处理化疗和异基因干细胞移植。在 2 例患者中,添加了针对 CD20 或 CD66 的 radioimmunotherapy,以增强抗淋巴瘤活性。终点是不良事件的发生率和严重程度、无进展生存期和总生存期。RLT 和额外的 radioimmunotherapy 耐受性良好,没有任何急性不良事件或生命体征变化。中位时间为 11 d(范围为 9-13 d)后记录到成功植入。在可进行随访的 4 例患者中(1 例患者在 RLT 后 29 d 死于中枢神经系统曲霉菌病,另 1 例患者在 RLT 后 34 d 死于再生障碍性败血症),2 例(均接受额外的 radioimmunotherapy)患者接受了 CXCR4 定向 RLT 治疗,结果为部分缓解,另外 2 例患者为混合反应。反应持续时间相当短暂,中位无进展生存期为 62 d(范围为 29-110 d),中位总生存期为 76 d(范围为 29-334 d)。在弥漫性大 B 细胞淋巴瘤中,在异基因干细胞移植前,CXCR4 导向的 RLT(联合额外的 radioimmunotherapy)是一种可行的预处理方案。

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