New trends in the use of radioimmunoconjugates for the therapy of cancer.

Targeted diagnosis and therapy Pub Date : 1990-01-01
D J Buchsbaum, T S Lawrence
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Abstract

Since 1980, there has been intense research in the area of radiolabeled immunoconjugates for the localization and therapy of cancer in both experimental animal models and in humans. This is based on the potential of MoAbs reactive with tumor-associated antigens as specific carriers of radionuclides, toxins, and chemotherapeutic drugs. Even though there has been much progress, a great deal of work and innovation will be required before the use of radiolabeled immunoconjugates becomes an established method for clinical tumor detection and therapy. The greatest problem is the relatively low tumor uptake of radiolabeled MoAbs in humans. This results in relatively high background levels of radioactivity in normal tissues and insufficient radioactivity in the tumor for the detection of small lesions and for therapeutic efficacy. In the future, one can expect the development of new MoAbs with greater specificity for particular tumor types, improvements in radiolabeling procedures, and the use of more effective nuclides than 131I. Biological, physiological, pathological, and dosimetric considerations need to be addressed in detail. With this additional information, it is hoped that the full potential for radiolabeled immunoconjugates will be realized.

放射免疫偶联物治疗癌症的新趋势。
自1980年以来,放射性标记免疫偶联物在实验动物模型和人类癌症定位和治疗方面的研究一直很激烈。这是基于MoAbs与肿瘤相关抗原反应的潜力,作为放射性核素、毒素和化疗药物的特定载体。尽管已经取得了很大的进展,但在使用放射标记免疫偶联物成为临床肿瘤检测和治疗的既定方法之前,还需要进行大量的工作和创新。最大的问题是人体对放射性标记的moab抗体的肿瘤摄取相对较低。这导致正常组织中的放射性水平相对较高,而肿瘤中的放射性不足以检测小病变和治疗效果。在未来,人们可以期待开发出对特定肿瘤类型具有更大特异性的新型moab,改进放射性标记程序,以及使用比131I更有效的核素。生物学、生理学、病理学和剂量学方面的考虑需要详细讨论。有了这些额外的信息,希望放射标记免疫偶联物的全部潜力将得到实现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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