Pietro Scilipoti, MD, of Ospedale San Raffaele, discusses the importance of incorporating life expectancy assessments into prostate cancer treatment decisions. He presented findings at the 2025 AUA Annual Meeting showing that comorbidity-based models offer more accurate risk evaluations than chronological age alone. Scilipoti emphasized that current guidelines lack validated tools for life expectancy assessment, which can lead to overtreatment or undertreatment. He advocates for prospective validation of these models and their inclusion in clinical trial design to better tailor treatments to patient risk profiles.
Amin Sobh, PhD, of the University of Florida College of Medicine, discussed findings from a study investigating the role that NSD2 plays in modulating immune surveillance in multiple myeloma. It is known that NSD2 is overexpressed in 15% of patients with multiple myeloma because of the t(4;14) translocation. Data shared during the 2025 AACR Annual Meeting suggested that NSD2 overexpression in this disease could suppress immune surveillance through downregulation of MHC-II expression in antigen-presenting immune cells. Moreover, increased IL10 production by NSD2 overexpressing multiple myeloma cells may underlie MHC-II suppression. Lastly, the effect of NSD2 overexpression and inhibition on immune microenvironment modulation of the bone marrow will be explored in immunocompetent mouse models of multiple myeloma.
Chad Tang, MD, of The University of Texas MD Anderson Cancer Center, shared data from a phase 2 trial (NCT03575611) evaluating metastasis-directed radiotherapy without systemic therapy in oligometastatic clear cell renal cell carcinoma. The trial included patients with clear cell histology, with up to 5 metastases, who had not previously received systemic therapy or were off previous systemic therapy for longer than a month. The co-primary end points were PFS and systemic therapy-free survival (STFS). The median PFS was 18 months (95% CI, 15-22) and the median STFS was 34 months (95% CI, 28-54). Moreover, the median overall survival (OS) was not reached, and the 3-year OS rate was 87%. Further trials are required to further evaluate this approach vs doublet systemic therapy.
Joseph Jacob, MD, MCR, of SUNY Upstate Medical University, discusses TAR-200 as a promising intravesical therapy that delivers sustained doses of gemcitabine directly to the bladder, potentially improving treatment outcomes for patients with high-risk, non–muscle-invasive bladder cancer. He presented phase 2b SunRISe-1 trial (NCT04640623) data at the 2025 AUA Annual Meeting, showing high complete response rates and durable outcomes in BCG-unresponsive patients. Jacob highlighted TAR-200’s potential to shift the standard of care by offering a bladder-sparing alternative to radical cystectomy. He also noted that this device-based platform could pave the way for delivering other intravesical agents in the future.