RT Book, Section A1 Dall’Era, Marc A. A2 Papadakis, Maxine A. A2 McPhee, Stephen J. A2 Rabow, Michael W. A2 McQuaid, Kenneth R. SR Print(0) ID 1193162603 T1 Prostate Cancer T2 Current Medical Diagnosis & Treatment 2023 YR 2023 FD 2023 PB McGraw-Hill Education PP New York, NY SN 9781264687343 LK accessmedicine.mhmedical.com/content.aspx?aid=1193162603 RD 2024/04/18 AB Key Clinical Updates in Prostate CancerMultiparametric MRI (mpMRI) has emerged as the imaging study of choice for localized prostate cancer detection and characterization. Suspicious prostatic lesions may then be sampled via MRI-guided needle biopsy or via MR Fusion (in which prostate MRI images are fused in real-time with images from an ultrasound-guided needle biopsy). Such an approach may improve discovery of potentially life-threatening disease while limiting overdetection of indolent prostate cancer or unnecessary prostate biopsies.NCCN guidelines recommend considering germline genetic testing in men presenting with localized high-risk, regionally advanced, or metastatic disease. Commercially available cancer tissue RNA-based assays are available for further risk assessment after prostate cancer diagnosis; these may help determine the need for and timing of prostate cancer treatment as well as treatment intensity.A secondary data analysis from the Prostate, Lung, Colorectal, and Ovarian trial demonstrated that baseline PSA for younger men in their 50s can predict long-term risk of prostate cancer and can be used to tailor PSA screening intervals.Active surveillance is now the preferred initial treatment recommendation for men with well-differentiated prostate cancer and low-risk clinical features.Results from the PEACE-1 trial demonstrate that a three-drug regimen, with androgen deprivation therapy, docetaxel and abiraterone acetate used together, provides the best survival outcome for men with hormone-naïve metastatic cancer. With this regimen, the median survival for men with de novo metastatic prostate cancer is now expected to be 5 years.Poly(ADP-ribose) polymerase (PARP) inhibitors represent a novel class of anticancer agents with some activity against prostate cancer particularly those harboring mutations in genes important for homologous recombination such as BRCA1, BRCA2, and ATM. There are two FDA-approved PARP inhibitors available for men with metastatic castrate-resistant prostate cancer with these genetic alterations.Kovac E et al. JAMA Netw Open. [PMID: 31940039]