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[177镥]帕妥珠单抗:HER-2表达异种移植瘤的实验性治疗

[177Lu]pertuzumab: experimental therapy of HER-2-expressing xenografts.

作者信息

Persson Mikael, Gedda Lars, Lundqvist Hans, Tolmachev Vladimir, Nordgren Hans, Malmström Per-Uno, Carlsson Jörgen

机构信息

Department of Biomedical Radiation Sciences, Rudbeck Laboratory, Uppsala University, SE-75185 Uppsala, Sweden.

出版信息

Cancer Res. 2007 Jan 1;67(1):326-31. doi: 10.1158/0008-5472.CAN-06-2363.

Abstract

Pertuzumab (Omnitarg) is a novel antibody against HER-2, domain II. HER-2 is a tyrosine kinase receptor that is overexpressed in several carcinomas, especially breast cancer. Pertuzumab, labeled with the low-energy beta emitter (177)Lu, might be a candidate for targeted radiotherapy of disseminated HER-2-positive micrometastases. The radiolabeled antibody [(177)Lu]pertuzumab showed favorable targeting properties in BALB/c (nu/nu) mice with HER-2-overexpressing xenografts. The absorbed dose in tumors was more than five times higher than the absorbed dose in blood and more than seven times the absorbed dose in any other normal organ. Experimental therapy showed that [(177)Lu]pertuzumab delayed tumor progression compared with controls (no treatment, P < 0.0001; nonlabeled pertuzumab antibody, P < 0.0001; and (177)Lu-labeled irrelevant antibody, P < 0.01). No adverse side effects of the treatment could be detected. Thus, the experimental results support the planning of clinical studies applying [(177)Lu]pertuzumab for therapy.

摘要

帕妥珠单抗(Omnitarg)是一种针对HER-2结构域II的新型抗体。HER-2是一种酪氨酸激酶受体,在多种癌症尤其是乳腺癌中过度表达。用低能β发射体(177)Lu标记的帕妥珠单抗可能是播散性HER-2阳性微转移灶靶向放疗的候选药物。放射性标记抗体[(177)Lu]帕妥珠单抗在过表达HER-2的异种移植BALB/c(nu/nu)小鼠中显示出良好的靶向特性。肿瘤中的吸收剂量比血液中的吸收剂量高五倍以上,比任何其他正常器官中的吸收剂量高七倍以上。实验性治疗表明,与对照组相比,[(177)Lu]帕妥珠单抗可延缓肿瘤进展(未治疗,P<0.0001;未标记的帕妥珠单抗抗体,P<0.0001;以及(177)Lu标记的无关抗体,P<0.01)。未检测到该治疗的不良副作用。因此,实验结果支持开展应用[(177)Lu]帕妥珠单抗进行治疗的临床研究规划。

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