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Review
. 2014 Aug;203(2):253-60.
doi: 10.2214/AJR.14.12554.

Molecular targeted α-particle therapy for oncologic applications

Affiliations
Review

Molecular targeted α-particle therapy for oncologic applications

Thaddeus J Wadas et al. AJR Am J Roentgenol. 2014 Aug.

Abstract

Objective: A significant challenge facing traditional cancer therapies is their propensity to significantly harm normal tissue. The recent clinical success of targeting therapies by attaching them to antibodies that are specific to tumor-restricted biomarkers marks a new era of cancer treatments.

Conclusion: In this article, we highlight the recent developments in α-particle therapy that have enabled investigators to exploit this highly potent form of therapy by targeting tumor-restricted molecular biomarkers.

Keywords: 213Bi; 223Ra; 225Ac; molecular radiotherapy; nuclear medicine; radioimmunotherapy; α-particle therapy.

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Figures

Fig. 1
Fig. 1
Illustration of monoclonal antibody conjugated to chemotherapeutic agent. Potentially toxic chemotherapeutic agents can be targeted to tumor-restricted biomarkers by attaching them to specific delivery systems, such as antibodies, that bring them directly to tumor cells and spare normal tissue from their deleterious effects. (Drawing by Mintz A)
Fig. 2
Fig. 2
Images show comparison of clearance of radiolabeled antibody versus peptide. A, Anterior whole-body planar scintigraphy of a 72-year-old man with suspected recurrent prostate cancer obtained 3 days after administration of 5.1 mCi (188.7 MBq) of 111In capromab pendetide (ProstaScint, Cytogen) antibody shows significant residual activity in blood pool (heart and great vessels) even 3 days after administration. B, Whole-body anterior (left) and posterior (right) planar images of a 49-year-old woman with a suspected gastrinoma obtained 4 hours after administration of 6.0 mCi (222.0 MBq) of 111In pentetreotide show little visible activity seen in blood pool (in regions of heart and great vessels) only hours after administration, in contrast to what is seen with high-molecular-weight antibodies (A). Images also show significant renal uptake as well as clearance into bladder.

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