Targeted α-particle radiotherapy with ²¹¹At-labeled monoclonal antibodies

Abstract 

An attractive feature of targeted radionuclide therapy is the ability to select radionuclides and targeting vehicles with characteristics that are best suited for a particular clinical application. One combination that has been receiving increasing attention is the use of monoclonal antibodies (mAbs) specifically reactive to receptors and antigens that are expressed in tumor cells to selectively deliver the α-particle-emitting radiohalogen astatine-211 (²¹¹At) to malignant cell populations. Promising results have been obtained in preclinical models with multiple ²¹¹At-labeled mAbs; however, translation of the concept to the clinic has been slow. Impediments to this process include limited radionuclide availability, the need for suitable radiochemistry methods operant at high activity levels and lack of data concerning the toxicity of α-particle emitters in humans. Nonetheless, two clinical trials have been initiated to date with ²¹¹At-labeled mAbs, and others are planned for the near future.

Keywords: Astatine-211, Radioimmunotherapy, Targeted radiotherapy, Monoclonal antibodies