Cancer Therapy with Alpha-Emitters Labeled Peptides

Ekaterina Dadachova

Research output: Contribution to journalReview article

29 Scopus citations

Abstract

Actively targeted α-particles offer specific tumor cell killing action with less collateral damage to surrounding normal tissues than β-emitters. During the last decade, radiolabeled peptides that bind to different receptors on the tumors have been investigated as potential therapeutic agents both in the preclinical and clinical settings. Advantages of radiolabeled peptides over antibodies include relatively straightforward chemical synthesis, versatility, easier radiolabeling, rapid clearance from the circulation, faster penetration and more uniform distribution into tissues, and less immunogenicity. Rapid internalization of the radiolabeled peptides with equally rapid re-expression of the cell surface target is a highly desirable property that enhances the total delivery of these radionuclides into malignant sites. Peptides, such as octreotide, α-melanocyte-stimulating hormone analogues, arginine-glycine-aspartic acid-containing peptides, bombesin derivatives, and others may all be feasible for use with α-emitters. The on-going preclinical work has primarily concentrated on octreotide and octreotate analogues labeled with Bismuth-213 and Astatine-211. In addition, α-melanocyte-stimulating hormone analogue has been labeled with Lead-212/Bismuth-212 in vivo generator and demonstrated the encouraging therapeutic efficacy in treatment of experimental melanoma. Obstacles that continue to obstruct widespread acceptance of α-emitter-labeled peptides are primarily the supply of these radionuclides and concerns about potential kidney toxicity. New sources and methods for production of these medically valuable radionuclides and better understanding of mechanisms related to the peptide renal uptake and clearance should speed up the introduction of α-emitter-labeled peptides into the clinic.

Original languageEnglish (US)
Pages (from-to)204-208
Number of pages5
JournalSeminars in nuclear medicine
Volume40
Issue number3
DOIs
StatePublished - May 2010

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging

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