Schottelius Margret, Wirtz Martina, Eiber Matthias, Maurer Tobias, Wester Hans-Jürgen
Chair for Pharmaceutical Radiochemistry, Technische Universität München, Walther-Meissner-Strasse 3, 85748, Garching, Germany.
Department of Nuclear Medicine, Klinikum rechts der Isar, Technische Universität München, Ismaningerstr. 22, 81675, Munich, Germany.
EJNMMI Res. 2015 Dec;5(1):68. doi: 10.1186/s13550-015-0147-6. Epub 2015 Nov 25.
The relevance of prostate-specific membrane antigen (PSMA) targeting in the clinical management of prostate cancer (PCa) is continually increasing, entailing the development of PSMA-targeted molecular probes. Recently, a first PSMA-targeted theranostic concept has been successfully implemented by [(68)Ga/(177)Lu]PSMA-I&T. To further exploit the excellent PSMA-targeting characteristics and in vivo performance of the PSMA-I&T platform, [(111)In]PSMA-I&T was evaluated as a complementary probe for radioguided surgery and SPECT imaging.
Compared to [(68)Ga/(177)Lu]PSMA-I&T, [(111)In]PSMA-I&T showed unchangedly high PSMA-affinity and enhanced internalization into PSMA-expressing LNCaP PCa cells. Biodistribution studies in LNCaP xenograft-bearing mice (1 h p.i.) revealed slightly reduced background accumulation of [(111)In]PSMA-I&T compared to [(177)Lu]PSMA-I&T and identical tumor uptake of both compounds, leading to increased tumor/background ratios for [(111)In]PSMA-I&T. An exemplary patient with metastatic PCa underwent preoperative [(68)Ga]HBED-CC-PSMA PET/CT (1 h p.i.) and [(111)In]PSMA-I&T SPECT/CT (4 h p.i.), followed by prostatectomy and radioguided extended pelvic lymphadenectomy (24 h p.i.). In [(111)In]PSMA-I&T SPECT/CT, the previously identified PCa lesions ([(68)Ga]HBED-CC-PSMA PET/CT) showed high tracer accumulation and were also detectable using planar scintigraphy. The intraoperative use of a hand-held gamma probe allowed detection and resection of all [(111)In]PSMA-I&T-accumulating lesions. The presence of PSMA-positive tumor tissue in the resected specimens was confirmed histopathologically and via [(111)In]PSMA-I&T autoradiography.
[(111)In]PSMA-I&T shows efficient PSMA targeting in vitro and in vivo, combined with low background accumulation. In an exemplary PCa patient, [(111)In]PSMA-I&T was successfully applied for preoperative SPECT/CT visualization and radioguided resection of PSMA-positive lesions, hinting towards a high value of [(111)In]PSMA-I&T as a complementary tool to [(68)Ga/(177)Lu]PSMA-I&T in the clinical management of prostate cancer.
前列腺特异性膜抗原(PSMA)靶向在前列腺癌(PCa)临床管理中的相关性不断增加,这促使了PSMA靶向分子探针的开发。最近,首个PSMA靶向的诊疗一体化概念已通过[(68)Ga/(177)Lu]PSMA-I&T成功实现。为了进一步利用PSMA-I&T平台出色的PSMA靶向特性和体内性能,[(111)In]PSMA-I&T被评估为放射性引导手术和SPECT成像的补充探针。
与[(68)Ga/(177)Lu]PSMA-I&T相比,[(111)In]PSMA-I&T显示出不变的高PSMA亲和力,并增强了对表达PSMA的LNCaP前列腺癌细胞的内化。对荷LNCaP异种移植瘤小鼠的生物分布研究(注射后1小时)显示,与[(177)Lu]PSMA-I&T相比,[(111)In]PSMA-I&T的背景蓄积略有减少,且两种化合物在肿瘤中的摄取相同,这导致[(111)In]PSMA-I&T的肿瘤/背景比值增加。一名转移性PCa患者在术前接受了[(68)Ga]HBED-CC-PSMA PET/CT(注射后1小时)和[(111)In]PSMA-I&T SPECT/CT(注射后4小时)检查,随后进行了前列腺切除术和放射性引导的扩大盆腔淋巴结清扫术(注射后24小时)。在[(111)In]PSMA-I&T SPECT/CT检查中,先前确定的PCa病变([(68)Ga]HBED-CC-PSMA PET/CT)显示出高示踪剂蓄积,并且使用平面闪烁显像也可检测到。术中使用手持式γ探针能够检测并切除所有[(111)In]PSMA-I&T蓄积的病变。切除标本中PSMA阳性肿瘤组织的存在通过组织病理学和[(111)In]PSMA-I&T放射自显影得以证实。
[(111)In]PSMA-I&T在体外和体内均显示出有效的PSMA靶向性,且背景蓄积较低。在一名示例性PCa患者中,[(111)In]PSMA-I&T成功应用于术前SPECT/CT可视化以及PSMA阳性病变的放射性引导切除,这表明[(111)In]PSMA-I&T作为[(68)Ga/(177)Lu]PSMA-I&T在前列腺癌临床管理中的补充工具具有很高的价值。