A brand new editorial paper was printed in Oncotarget’s Quantity 15 on July 2, 2024, entitled, “Utilizing early on-treatment circulating tumor DNA measurements as response evaluation in metastatic castration resistant prostate most cancers.”
On this new editorial, researchers S.H. Tolmeijer, E. Boerrigter, N.P. Van Erp, and Niven Mehra from Radboud College Medical Heart talk about metastatic castration resistant prostate most cancers (mCRPC). mCRPC is deadly, however the variety of life-prolonging systemic remedies out there for mCRPC has expanded over time. Actual world information recommend that the commonest first-line remedy for mCRPC was therapy with an androgen receptor pathway inhibitor (ARPI), being both enzalutamide or abiraterone, though extra sufferers will these days obtain ARPI and/or docetaxel already for hormone delicate prostate most cancers (HSPC).
Current medical trial information recommend potential advantage of including poly-ADP ribose polymerase inhibitors (PARPi) or lutetium-117-prostate-specific membrane antigen (LuPSMA) to first-line mCRPC therapy with ARPIs in a subset of sufferers. As these totally different drug lessons are related to totally different toxicity profiles and vital prices, it’s extremely necessary to establish which sufferers expertise sturdy profit from monotherapy ARPI and which sufferers would probably profit from therapy intensification or remedy change.
“Analysis by Tolmeijer et al. 2023, printed in Scientific Most cancers Analysis, means that the detection of circulating tumor DNA (ctDNA) at baseline and 4-weeks after therapy initiation can predict response sturdiness to first-line ARPIs.”
Supply:
Journal reference:
S.H. Tolmeijer, et al. (2024). Utilizing early on-treatment circulating tumor DNA measurements as response evaluation in metastatic castration resistant prostate most cancers. Oncotarget. doi.org/10.18632/oncotarget.28599.

