Herrmann Ken, Schottelius Margret, Lapa Constantin, Osl Theresa, Poschenrieder Andreas, Hänscheid Heribert, Lückerath Katharina, Schreder Martin, Bluemel Christina, Knott Markus, Keller Ulrich, Schirbel Andreas, Samnick Samuel, Lassmann Michael, Kropf Saskia, Buck Andreas K, Einsele Hermann, Wester Hans-Juergen, Knop Stefan
Department of Nuclear Medicine, University Hospital Würzburg, Würzburg, Germany Department of Molecular and Medical Pharmacology, David Geffen School of Medicine at UCLA, Los Angeles, California Jonsson Comprehensive Cancer Center, David Geffen School of Medicine at UCLA, Los Angeles, California
Pharmaceutical Radiochemistry, Technische Universität München, Munich, Germany.
J Nucl Med. 2016 Feb;57(2):248-51. doi: 10.2967/jnumed.115.167361. Epub 2015 Nov 12.
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.
趋化因子受体4(CXCR4)是多种人类癌症中肿瘤生长和转移的关键因素。基于放射性标记的CXCR4配体((68)Ga-喷替沙氟)用于诊断性受体靶向的良好经验,(177)Lu-和(90)Y-喷替沙肽最近被开发为内照射治疗载体。在此,我们总结了3例接受CXCR4导向内照射治疗的多发性骨髓瘤患者的人体首例经验,这些患者均有髓内和广泛髓外表现且经过大量预处理。
通过基线(68)Ga-喷替沙氟PET证实CXCR4靶点表达。每次治疗均经临床伦理委员会批准。在给予(177)Lu-喷替沙肽或(90)Y-喷替沙肽治疗前进行治疗前(177)Lu-喷替沙肽剂量测定。随后,患者接受额外的化疗和自体干细胞移植以进行骨髓挽救。
2例患者显示出显著的治疗效果,(18)F-FDG摄取显著降低。
喷替沙肽靶向CXCR4的放疗与细胞毒性化疗和自体干细胞移植联合应用似乎是一种有前景的新型治疗选择,尤其适用于晚期多发性骨髓瘤患者。