Relative therapeutic efficacy of 125I- and 131I-labeled monoclonal antibody A33 in a human colon cancer xenograft

被引:1
作者
Barendswaard, EC
Humm, JL
O'Donoghue, JA
Sgouros, G
Finn, RD
Scott, AM
Larson, SM
Welt, S
机构
[1] Ludwig Inst Canc Res, New York Branch, New York, NY USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med Phys, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Nucl Med Sect, New York, NY 10021 USA
[4] Mem Sloan Kettering Canc Ctr, Clin Immunol Serv, New York, NY 10021 USA
关键词
radiolabeled mAb A33; targeting; colon cancer xenograft; therapeutic efficacy;
D O I
暂无
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
A33, a monoclonal antibody that targets colon carcinomas, was labeled with I-125 or I-131 and the relative therapeutic efficacy of the 2 radiolabeled species was compared in a human colon cancer xenograft system. Methods: Nude mice bearing human SW1222 colon carcinoma xenografts were administered escalating activities of I-125-A33 (9.25-148 MBq) or I-131-A33 (0.925-18.5 MBq), I-125- and I-131-labeled control antibodies, unlabeled antibody, or no antibody. The effects of treatment were assessed using the endpoints of tumor growth delay and cure. Results: Tumor growth delay increased with administered activity for all radiolabeled antibodies. Approximately 4.5 times more activity was required for I-125-A33 to produce therapeutic effects that were equivalent to those of I-131-A33. This ratio was approximately 7 for a nonspecific, noninternalizing isotype-matched, radiolabeled control antibody. Unlabeled A33 antibody had no effect on tumor growth. Approximately 10 times more activity of I-125-A33 produced toxicity similar to that of I-131-A33, and this ratio fell to approximately 6 for radiolabeled control antibody. Conclusion: Treatment with I-125-A33 resulted in a relative therapeutic gain of approximately 2 compared with I-131-A33 in this experimental system.
引用
收藏
页码:1251 / 1256
页数:6
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