Pluvicto™, was approved by the FDA. Pluvicto, lutetium Lu 177 vipivotide tetraxetan (formerly referred to as 177Lu-PSMA-617) is the first approved targeted radioligand therapy for the treatment of men with progressive, PSMA‑positive metastatic castration-resistant prostate cancer.
Node Positive Prostate Cancer – Treatment and Survival
Orgovyx - The Newest Hormone Treatment (ADT) for Prostate Cancer
Bipolar Androgen Therapy Effective in Metastatic Castration-Resistant Prostate Cancer
Metformin Added to Hormone Therapy (ADT) Has Positive Effects on Prostate Cancer
PYLARIFY PSMA PET Scan FDA Approved for Prostate Cancer
Every Drug Has Two Names - Understanding the Prostate Cancer Drug Names
Black Men's Prostate Cancer May Be More Responsive to Immunotherapy – Why
Have a BRCA2 Mutation? Activating Your Immune System Could Be A Promising Cancer Treatment Option
Hope - Maybe Changing Hormone Therapy?
177Lu-PSMA-617 Theranostics Might Be More Active and Safer than Cabazitaxel
Bipolar Androgen Therapy vs. Enzalutamide in Asymptomatic Men With Castration-Resistant Metastatic Prostate Cancer
In this study comparing BAT to Enza after Zytiga failure, the researchers found a response of approximately 28%. BAT demonstrated a clinically superior activity level compared with Enza. It also was associated with the same progression-free survival and numerically more prolonged PSA progression-free survival and overall survival.
Optimal Chemo-Hormonal Sequencing for mCRPC Maybe Taxotere – Zytiga – Jevtana – Xtandi
FDA Approves An Oral Hormone Therapy (ADT)
The Food and Drug Administration has approved a new drug for men with advanced prostate cancer. The approval is for a first in kind hormone therapy (ADT) taken orally (by mouth) instead of the regular Lupron type injections we have been using.
Besides achieving and maintaining adequate levels of castration, Orgovyx was also superior to Lupron because it cut the incidence of serious heart events compared to Lupron.
FDA Approves Gallium 68 PSMA PET Scan
Understanding the PARP Inhibitors - Who Will Benefit?
LYNPARZA (olaparib) and RUBRACA (rucaparib) are PARP Inhibitors that were FDA approved in May of 2020 for men with castrate resistant prostate cancer who also have certain genetic mutations. The FDA also approved certain Companion Diagnostic genetic tests to go along with the decision making to use these PARP Inhibitors.
There is a lot of information now available with these recent developments which makes decision making confusing.