
Arvin George, MD, highlights VAPOR 2 trial of thermal water therapy for prostate cancer
Arvin K. George, MD, discusses the unique design of the VAPOR 2 trial and the key findings from the first 110 patients enrolled.
Interim data from the VAPOR 2 trial (NCT05683691) were presented at the 2025
The Vanquish System was granted FDA 510(k) clearance on December 2, 2025 for prostate tissue ablation.2
In a recent interview with Urology Times®, presenting author Arvin K. George, MD, detailed the unique design of the VAPOR 2 trial and the key findings from the first 110 patients enrolled. George is a urologic oncologist, director of prostate cancer programs, and an associate professor of clinical urology at Johns Hopkins Medicine in Baltimore, Maryland.
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At the time of the data report, 110 patients were enrolled in the study. In total, the trial intends to enroll 235 patients across 26 clinical trial sites in the US.
At 6 months, 91% of eligible patients (n = 110) showed no targeted MRI visible intermediate-risk disease following a single Vanquish procedure. According to the company, “the Vanquish System demonstrated the ability to effectively treat cancerous lesions in all prostate locations, addressing a significant limitation of existing ablative options.”2
Treatment was also well-tolerated, with no device-related serious adverse events and low rates of urinary incontinence and erectile dysfunction.
REFERENCES
1. George A. Thermal water therapy for the management of prostate cancer: the VAPOR 2 study. interim analysis. Presented at: Society of Urologic Oncology Annual Meeting; December 2-5, 2025; Phoenix, Arizona. Abstract 260.
2. Francis Medical receives FDA 510(k) clearance for use of the Vanquish Water Vapor System for prostate tissue ablation. News release. Francis Medical Inc. December 2, 2025. Accessed December 8, 2025.
















