
EVP With Consolidative Surgery Yields Promising Outcomes in Bladder Cancer
Enfortumab vedotin plus pembrolizumab followed by surgery showed high complete response rates in advanced urothelial cancer.
Consolidative surgery following treatment with enfortumab vedotin (Padcev) plus pembrolizumab (Keytruda; EVP) appears to be feasible, leading to high complete response rates in patients with advanced urothelial carcinoma, according to a retrospective cohort study.1
Data from this study were presented in a poster at the
Patient Characteristics
Of the 15 patients included in the analysis, the median age was 69 years, 67% of patients were male, and all had an ECOG performance status of 0 or 1. Five were ineligible for cisplatin due to renal impairment (n = 4) or hearing loss (n = 1).
Five patients presented with T2 disease, 9 with T3, and 1 with T4. Of the 9 patients who achieved T0 disease, 1 started with T4, 4 started with T3, and 4 started with T2. Two patients downstaged from T3 to T2 disease, and 2 patients went from T3 to Ta-is.
The median number of cycles of EVP before surgery was 4, and the median interval from initiation of EVP to surgery was 16 weeks. The average length of hospital stay was 5 days for radical cystectomy and 4 days for nephroureterectomy or distal ureterectomy.
Safety and Complications
A total of 10 complications were recorded. In patients who underwent cystectomy (n = 9), these included 1 incidence each of Clavien-Dindo grade 1 shortness of breath; grade 2 prolonged ileus, sepsis, urinary tract infection, and wound dehiscence; and grade 3 failure to thrive and ascites. In patients who underwent nephroureterectomy or distal ureterectomy (n = 6), the observed complications were 1 incidence each of grade 1 leg swelling, grade 2 cystitis, and grade 3 obstructive uropathy. Further, there was no 90-day mortality.
About EVP
In April 2023, the FDA granted an
The expanded approval was supported by findings from the EV-302/KN-A39 (NCT04223856) trial.3 Here, EVP demonstrated statistically significant improvements to overall survival (OS) and progression-free survival (PFS) compared with platinum-based chemotherapy. The median OS was 31.5 months (95% CI, 25.4-not estimable) vs 16.1 months (95% CI, 13.9-18.3) with EVP and chemotherapy, respectively (HR, 0.47; 95% CI, 0.38-0.58; P<.0001). The median PFS was 12.5 months (95% CI, 10.4-16.6) with EVP vs 6.3 months (95% CI, 6.2-6.5) with chemotherapy (HR, 0.45; 95% CI, 0.38-0.54; P <.0001).
Recently, at the 2025 Genitourinary Cancers Symposium,





































