[ 177 Lu]Lu-PSMA-617 (Pluvicto TM ): The First FDA-Approved Radiotherapeutical for Treatment of Prostate Cancer.
Ute HennrichMatthias EderPublished in: Pharmaceuticals (Basel, Switzerland) (2022)
In March 2022, [ 177 Lu]Lu-PSMA-617 (Pluvicto TM ) was approved by the FDA for the treatment of prostate cancer patients. Until now, the approval has been limited to patients with PSMA-positive metastatic castration-resistant prostate cancer who have previously received other therapy options (such as inhibition of the androgen receptor pathway and taxane-based chemotherapy). [ 177 Lu]Lu-PSMA-617, which combines a PSMA-specific peptidomimetic with a therapeutical radionuclide, is used in a radioligand therapy that selectively delivers ionizing radiation to tumor cells, causing their death, while sparing the surrounding healthy tissue. In numerous clinical trials, the efficacy of [ 177 Lu]Lu-PSMA-617 was demonstrated.