Targeted Radiopharmaceutical Therapy for Prostate Cancer (Pluvicto)
Prostate-specific membrane antigen (PSMA)-targeted radiopharmaceutical therapy is an FDA-approved treatment for castrate-resistant metastatic prostate cancer. This drug is known by the brand name Pluvicto.
In PSMA-targeted therapy, a radiopharmaceutical is infused into the bloodstream through an IV. It seeks out and attaches to the PSMA protein on prostate cancer cells wherever they might be located throughout the body. It then delivers a microscopic amount of radiation directly to the prostate cancer cells, killing them with minimal harm to surrounding healthy tissue.
As of 2025, ARA is using Pluvicto (lutetium-177 vipivotide tetraxetan), which has been approved by the FDA for treatment of prostate cancer.
The full treatment is given as six separate infusions, six weeks apart. During the treatment, you will remain under the care of your primary cancer care provider, and you will come to the ARA Theranostics Center every six weeks for your infusion.
PSMA-targeted therapy may be life-extending for patients with metastatic prostate cancer.
To qualify for the PSMA-targeted treatment under current guidelines, patients will need to have been treated with androgen deprivation therapy (ADT).
If you are interested in finding out if you are qualified for the treatment, please fill out our Pluvicto Patient Intake Form.
How Does PSMA-targeted Therapy (Pluvicto) Work?
1) The PSMA-targeted radiopharmaceutical Pluvicto, which contains lutetium-177, is infused through an IV. 2) It seeks out prostate cells (in black) anywhere they have metastasized in the body. 3) It attaches to the prostate cancers and delivers a microscopic amount of radiation to the cancer cells. 4) The radiation kills the cancer cells, leaving surrounding healthy tissue (in white) unharmed.