CXCR4型
多发性骨髓瘤
医学
化疗
移植
转移
放射治疗
干细胞
肿瘤科
骨髓
癌症研究
癌症
内科学
核医学
病理
受体
生物
趋化因子
遗传学
作者
Ken Herrmann,Margret Schottelius,Constantin Lapa,Theresa Osl,Andreas Poschenrieder,Heribert Hänscheid,Katharina Lückerath,Martin Schreder,Christina Bluemel,Markus Knott,Ulrich Keller,Andreas Schirbel,Samuel Samnick,Michael Laßmann,Saskia Kropf,Andreas K. Buck,Hermann Einsele,Hans‐Juergen Wester,Stefan Knop
标识
DOI:10.2967/jnumed.115.167361
摘要
Chemokine receptor 4 (CXCR4) is a key factor for tumor growth and metastasis in several types of human cancer. Based on promising experiences with a radiolabeled CXCR4 ligand ((68)Ga-pentixafor) for diagnostic receptor targeting, (177)Lu- and (90)Y-pentixather were recently developed as endoradiotherapeutic vectors. Here, we summarize the first-in-human experience in 3 heavily pretreated patients with intramedullary and extensive extramedullary manifestations of multiple myeloma undergoing CXCR4-directed endoradiotherapy.CXCR4 target expression was demonstrated by baseline (68)Ga-pentixafor PET. Each treatment was approved by the clinical ethics committee. Pretherapeutic (177)Lu-pentixather dosimetry was performed before (177)Lu-pentixather or (90)Y-pentixather treatment. Subsequently, patients underwent additional chemotherapy and autologous stem cell transplantation for bone marrow rescue.A remarkable therapeutic effect was visualized in 2 patients, who showed a significant reduction in (18)F-FDG uptake.CXCR4-targeted radiotherapy with pentixather appears to be a promising novel treatment option in combination with cytotoxic chemotherapy and autologous stem cell transplantation, especially for patients with advanced multiple myeloma.
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