Abstract

Preclinical PET imaging studies with 124I-CLR1404, a radioiodinated phospholipid ether analog, indicate selective tumor uptake and prolonged tumor retention in 52/54 solid cancers. The agent does not localize in either inflammatory sites or premalignant lesions and thus affords excellent promise for therapy of solid malignancies due to its prolonged tumor cell retention properties. The overall objective of this study was to evaluate the therapeutic efficacy of 131I-CLR1404 in a variety of solid human xenograft cancer models.

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