Pretargeted Radioimmunotherapy in Cancer: An Overview
Abstract
The concept of tumour targeting began at the turn of the twentieth century when Ehrlich (1907) postulated the idea of the “Magic Bullet” to target abnormal cells selectively on the basis of antigenic differences between normal and abnormal cells. No clinical application of this concept took place until Pressman and Keighley (1948) utilized labeled antibodies for cancer detection. Pressman et al. (1957) showed that monoclonal antibodies (MoAbs) labeled with radioactive iodine could be used in animals on a diagnostic basis. Later, Bale et al. (1960) demonstrated that tumour localizing antibodies could be used as a therapeutic agent for treating experimental neoplasms by means of the radioactivity. The modern era of targeted cancer therapy did not start until 1975, upon the publication of Kohler and Milstein’s (1975) work describing the technology for the production of MoAbs, also referred to as the “hybridoma technology”. This method allowed the production of a large amount of different MoAbs with high specificity towards tumour-associated antigens and opened the door to the preclinical and clinical research in the targeted radiotherapy of cancer using MoAbs, referred to as radioimmunotherapy (RIT).
Keywords
Anaplastic Astrocytoma Linear Energy Transfer Relative Biologic Effectiveness Radionuclide Therapy Bispecific AntibodyReferences
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