Effectiveness and safety of first-line atezolizumab in locally advanced or metastatic urothelial cancer: The IMFLAME study.
Abstract
720 Background: Urothelial cancer (UC) is the tenth most common cancer globally. Standard first-line treatment for metastatic UC (mUC) involves enfotumab-vedotin + pembrolizumab or platinum-based chemotherapies, but some patients are ineligible to standard treatment due to significant comorbidities and poor performance status. Atezolizumab, an immune checkpoint inhibitor, has shown activity in clinical trials. This study evaluates the real-world effectiveness and safety of atezolizumab as a first-line treatment in patients with locally advanced or metastatic UC ineligible for platinum-based chemotherapies. Methods: This retrospective, multicenter, observational study included 91 patients with locally advanced or mUC treated with atezolizumab monotherapy as first-line treatment in Spain. Data were extracted from medical charts, including patient demographics, clinical characteristics, treatment patterns, and outcomes. The primary endpoint was the 12-month survival rate. Secondary endpoints included overall survival (OS), progression-free survival (PFS), objective response rate (ORR), duration of response (DoR), and safety profile. Results: The median age at diagnosis of mUC was 77 years, and 90.1% of patients had mUC. The population had a high burden of comorbidities, 90,1% had at least 1 comorbidity, 30% of the patients had PS ECOG ≥ 2 and 42.9% had visceral metastases. The 12-month survival rate was 41.8%, decreasing to 30.8% and 19.8% at 18 and 24 months, respectively. The ORR was 45.2%, with a median DoR of 19 months (95% CI: 9.8-28.3). The median PFS was 4.1 months, and the median OS was 9.7 months. According to multivariate COX regression analysis, PS ECOG ≥ 2 was an independent prognostic factor for worse survival. Safety analysis revealed that 26.4% of patients required treatment interruption due to treatment related adverse events (TRAEs), with immune-related adverse events (irAEs) occurring in 12.1% of patients, only 6% of patients discontinued treatment due to an irAEs. Conclusions: First-line atezolizumab monotherapy provides a clinically relevant benefit in terms of response, PFS, and OS in patients with locally advanced or metastatic UC ineligible for platinum-based chemotherapies. Despite the high burden of comorbidities and poor prognosis in this population, atezolizumab demonstrated an acceptable safety profile. These findings support the use of atezolizumab in platinum-ineligible patients and potentially in those who are not suitable for EV-Pembrolizumab under routine clinical practice conditions and highlight the need for further research to optimize patient selection and management. Outcome Measure Value 95% CI 12-month survival rate (%) 41.8 33.5-55.3 18-month survival rate (%) 30.8 23.4-44.5 24-month survival rate (%) 19.8 13.6-32.5 Overall Response Rate (%) 45.2 Median PFS (months) 4.1 Median OS (months) 9.7
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (19)
Alfonso Gomez De Liaño Lista
Medical Oncology Department - Complejo Hospitalario Universitario Insular-Materno Infantil, Universidad de Las Palmas de Gran Canaria, Las Palmas De Gran Canaria, Spain
Nuria Romero-Laorden
Hospital Universitario de la Princesa, Madrid, Spain
Pablo Gajate
Medical Oncology, Hospital Universitario Ramón y Cajal, Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain
Alberto Orta-Ruiz
Department of Medical Oncology, MD Anderson Cancer Center Madrid, Madrid, Spain
Jesús García-Donas Jiménez
Medical Oncology Department, Centro Integral Oncológico Clara Campal (CIOCC), Madrid, Spain
Maria Jose Miranda
Medical Oncology Department, Institut d’Oncologia de la Catalunya Sud (IOCS). Hospital Universitari Sant Joan de Reus. IISPV. URV, Tarragona, Spain
Sergio Vázquez Estévez
Carmen Molins
Medical Oncology Department, University Hospital Dr. Peset, Valencia, Spain
Cristina Pernaut
Medical Oncology Department, University Hospital Severo Ochoa, Leganés, Spain
Marta González Cordero
Hospital Universitario de Badajoz, Badajoz, Spain
Ovidio Fernández
Complexo Hospitalario Universitario de Ourense, Ourense, Spain
Jose García Sánchez
Medical Oncology Department, University Hospital Arnau de Vilanova-Liria, FISABIO, Valencia, Spain
Iria Gonzalez Maeso
Hospital Son Llatzer, Mallorca, Spain
Patricia Rodríguez Blázquez
Medical Oncology Department, University Hospital Lluis Alcañiz de Xàtiva, Valencia, Spain
Oscar Reig
Medical Oncology, Hospital Clinic and Translational Genomics and Targeted Therapies in Solid Tumors Group, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain
Pablo Maroto-Rey
Hospital de la Santa Creu i Sant Pau, Barcelona, Spain
Almudena Martin
Hospital Universitario Infanta Leonor, Madrid, Spain
Ignacio Ramirez
Medical Department, Roche Farma S.A., Madrid, Spain
Javier Puente
Hospital Clínico Universitario San Carlos de Madrid, Madrid