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PROs in advanced uc patients ineligible for cisplatin: first-line enfortumab vedotin ± pembrolizumab [Video]

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Pediatric Cancer

PROs in advanced uc patients ineligible for cisplatin: first-line enfortumab vedotin ± pembrolizumab

Jonathan Rosenberg, MD, Memorial Sloan Kettering Cancer Center in New York, NY, presents findings from Cohort K of the Phase Ib/II EV-103 trial (NCT03288545), assessing the impact of first-line enfortumab vedotin (EV) alone or with pembrolizumab on quality of life (QOL), functioning, and symptoms in patients with locally advanced/metastatic urothelial cancer (la/mUC) who were cisplatin-ineligible. In this phase Ib/II trial, patients were randomly assigned to EV plus pembrolizumab or EV monotherapy. Patient-reported outcomes (PROs) were assessed using the EORTC QLQ-C30 and BPI-SF. Results showed maintenance or improvement of QOL/functioning/symptoms with EV plus pembrolizumab, with clinically meaningful improvements in pain observed in both arms. These findings complement clinical outcomes of first-line EV plus pembrolizumab. This interview took place at the American Association for Cancer Research (AACR) Annual Meeting 2024 in San Diego, CA.

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