ASCO 2026: PROs from IMvigor011: A Phase 3 Study of ctDNA-Guided Adjuvant Atezolizumab vs Placebo in MIBC

(UroToday.com) The 2026 American Society of Clinical Oncology Genitourinary (ASCO) Annual Meeting, held in Chicago, IL, will host the Kidney and Bladder Cancer - Posters. Dr. Joaquim Bellmunt will present Abstract 4627: Patient-reported outcomes (PROs) from IMvigor011: A phase 3 study of ctDNA-guided adjuvant atezolizumab vs placebo in MIBC.

The phase 3 IMvigor011 trial previously demonstrated that serial ctDNA-based molecular residual disease (MRD) monitoring could identify patients with MIBC at very high risk of recurrence who derive significant benefit from adjuvant atezolizumab, while patients who remained persistently ctDNA-negative had low recurrence and mortality risk without adjuvant treatment.1 In this presentation, he focused on patient-reported outcomes (PROs) from the study, evaluating whether ctDNA-guided adjuvant atezolizumab impacted quality of life.

Patients with MIBC and no radiographic evidence of disease after cystectomy underwent serial ctDNA monitoring for up to one year. Patients who tested ctDNA-positive and remained disease-free were randomized to atezolizumab or placebo every four weeks for up to 12 cycles or one year. PROs were assessed longitudinally using the EORTC QLQ-C30 and IL46 questionnaires.

Among 250 ctDNA-positive patients randomized to atezolizumab (n=167) or placebo (n=83), questionnaire completion rates remained high throughout treatment. Time to confirmed deterioration (TTCD) analyses demonstrated no significant differences between arms for physical functioning, role functioning, or global health status/quality of life. Median TTCD for global health status/QoL was 35.4 months with atezolizumab versus 16.5 months with placebo (HR 0.71, 95% CI 0.45–1.12). Similarly, no clinically meaningful differences were observed in symptom burden or functional outcomes over time between treatment arms.

More than 90% of patients in both treatment arms reported little or no treatment-related side-effect burden from Cycle 1 Day 1 through Cycle 11 Day 1. At Cycle 11 Day 1, 98.3% of patients receiving atezolizumab reported “not at all/a little” treatment burden, with no patients reporting “very much” side-effect burden.

Key Messages:

  • ctDNA-guided adjuvant atezolizumab provided clinically meaningful DFS and OS benefit in ctDNA-positive patients with MIBC
  • Adjuvant atezolizumab did not negatively impact patient-reported quality of life compared with placebo
  • Longitudinal PRO analyses demonstrated preserved physical functioning, role functioning, and global health status/QoL
  • More than 90% of patients reported little or no treatment-related side-effect burden throughout treatment
  • These findings further support a biomarker-driven perioperative strategy in MIBC using serial ctDNA monitoring

Presented by: Joaquim Bellmunt, MD, PhD, Medical Oncologist, Director, Bladder Cancer Center, Dana Farber Cancer Institute, Boston, MA

Written by: Julian Chavarriaga, MD, Clinical Assistant Professor, Urologic Oncologist, Department of Urology at Penn State Health @chavarriagaj on X during the American Society of Clinical Oncology Genitourinary (ASCO) Annual Meeting held in Chicago, IL between May 29th and June 1st, 2026  

Reference:

  1. Powles T, Kann AG, Castellano D, Gross-Goupil M, Nishiyama H, Bracarda S, Bjerggaard Jensen J, Makaroff L, Jiang S, Ku JH, Park SH, Reig Torras O, Ye D, Maruzzo M, Necchi A, Morales-Barrera R, Giunta EF, Lee JL, Tortora G, Ürün Y, Dolowy L, Erdem D, Pinto A, Grando F, Zou W, Assaf ZJ, Vuky J, Degaonkar V, Steinberg EE, Bellmunt J, Gschwend JE; IMvigor011 Investigators. ctDNA-Guided Adjuvant Atezolizumab in Muscle-Invasive Bladder Cancer. N Engl J Med. 2025 Dec 18;393(24):2395-2408. doi: 10.1056/NEJMoa2511885. Epub 2025 Oct 20. PMID: 41124204.