ASCO Annual Meeting 2026

McCormick Place, Chicago, IL, USA

May 29 - June 2, 2026

 

ASCO Annual Meeting 2026
ASCO Annual Meeting 2026

Enfortumab Vedotin

Neoadjuvant and adjuvant enfortumab vedotin plus pembrolizumab for participants with muscle-invasive bladder cancer who are eligible for cisplatin: randomized, open-label, phase 3 KEYNOTE-B15 study.*

Christopher J. Hoimes, DO

Note that the poster includes new data and is entitled “Exploratory Subgroup Outcomes in the Phase 3 KEYNOTE-B15 Study of Neoadjuvant-Adjuvant Enfortumab Vedotin Plus Pembrolizumab for Participants With Muscle-Invasive Bladder Cancer Eligible for Cisplatin”.

Health-related quality of life with neoadjuvant and adjuvant enfortumab vedotin plus pembrolizumab in participants with muscle-invasive bladder cancer who are cisplatin ineligible: phase 3 KEYNOTE-905 study.

Peter H. O'Donnell, MD

Neoadjuvant and adjuvant enfortumab vedotin plus pembrolizumab in participants with cisplatin-ineligible muscle-invasive bladder cancer: an analysis of clinically relevant subgroups in KEYNOTE-905.

Nabil Adra, MD

Enfortumab vedotin plus pembrolizumab vs chemotherapy for previously untreated locally advanced or metastatic urothelial carcinoma: 3.5-year follow-up and response analyses from the phase 3 EV-302 study.

Thomas Powles, MD, PhD, FCRP


Enzalutamide

Efficacy and safety of enzalutamide in patients with metastatic hormone-sensitive prostate cancer (mHSPC) and cardiometabolic comorbidities and/or related concomitant medications: ARCHES post hoc.

Arnulf Stenzl, MD

Predictors of treatment duration in patients with metastatic hormone-sensitive prostate cancer (mHSPC) treated with enzalutamide: a post hoc analysis of ARCHES.

Andrew J. Armstrong, MD, MS

EMBARK: Testosterone recovery to >250 ng/dL following treatment suspension.

Stephen J. Freedland, MD

Outcomes with androgen-deprivation therapy plus androgen receptor pathway inhibitors in veterans with de novo metastatic castration-sensitive prostate cancer (mCSPC) who were elderly, frail, or had high comorbidity: a subgroup analysis of enzalutamide and high-volume disease.

Martin W. Schoen, MD, MPH


Fezolinetant

HIGHLIGHT 1: A randomized, placebo-controlled, double-blind, phase 3 clinical study to investigate the efficacy and safety of fezolinetant for treatment of moderate to severe vasomotor symptoms (hot flashes) in women with stage 0 to 3 hormone receptor-positive breast cancer who are receiving adjuvant endocrine therapy.

Céline Bouchard, MD