III. Medical Department, Hematology and Medical Oncology, Technische Universität München, Munich, Germany.
Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany.
J Nucl Med. 2019 Oct;60(10):1399-1405. doi: 10.2967/jnumed.118.223420. Epub 2019 Mar 8.
The chemokine receptor CXC-chemokine receptor 4 (CXCR4) is a transmembrane receptor involved in survival, proliferation, and dissemination of different cancers, including hematopoietic malignancies. Relapsed or refractory hematopoietic cancers are frequently resistant to conventional therapy, and novel highly active strategies are urgently needed. CXCR4-directed endoradiotherapy constitutes a highly promising targeted therapeutic concept. Here, we investigated the adverse effects of this novel treatment approach. Twenty-two patients with heavily pretreated lymphoproliferative or myeloid malignancies were treated with Lu- or Y-pentixather-a CXCR4-directed therapeutic radioligand-before conventional conditioning therapy followed by autologous or allogeneic hematopoietic stem cell transplantation. Twenty-five CXCR4-directed endoradiotherapies were administered to those patients. Adverse events occurring between endoradiotherapy and the start of conventional conditioning therapy were retrospectively analyzed and graded for the estimation of the safety profile. CXCR4-directed endoradiotherapy with pentixather showed a favorable toxicity profile. As expected, the hematopoietic system was most affected, with all subjects developing cytopenias. Except for 1 acute kidney failure, grade 3, due to tumor lysis syndrome, overall nephro- and hepatotoxicity was low. Other higher-grade adverse events were either transient and resolved or easily manageable. Therapy with radiolabeled pentixather appears to be well tolerated and easily applicable when preceding conventional conditioning regimens for hematopoietic stem cell transplantation.
趋化因子受体 CXC-趋化因子受体 4(CXCR4)是一种参与不同癌症(包括血液恶性肿瘤)的存活、增殖和扩散的跨膜受体。复发或难治性血液癌症通常对常规治疗具有抗性,因此迫切需要新的高度有效的策略。CXCR4 导向的内放射治疗构成了一种极具前景的靶向治疗概念。在这里,我们研究了这种新治疗方法的不良反应。
22 例经大量预处理的淋巴增殖性或髓性恶性肿瘤患者在接受常规预处理治疗前,接受了 Lu 或 Y-戊曲肽-a CXCR4 导向的治疗放射性配体治疗,随后进行自体或同种异体造血干细胞移植。对这些患者进行了 25 次 CXCR4 导向的内放射治疗。回顾性分析了内放射治疗与常规预处理治疗开始之间发生的不良事件,并对其进行分级,以评估安全性概况。
用戊曲肽进行的 CXCR4 导向的内放射治疗显示出良好的毒性特征。正如预期的那样,造血系统受到的影响最大,所有患者均出现细胞减少症。除了 1 例因肿瘤溶解综合征导致的 3 级急性肾衰竭外,总体肾毒性和肝毒性较低。其他较高等级的不良事件要么是短暂的且已解决,要么是易于管理的。
当用于造血干细胞移植的常规预处理方案之前时,放射性标记的戊曲肽治疗似乎具有良好的耐受性,并且易于应用。