Long-term survival following anti-PD-(L)1 monotherapy in advanced urothelial cancer and an assessment of potential prognostic clinical factors: a multicentre observational study
Chantal F. Stockem,
Sarah M. H. Einerhand,
Isabel Miras Rodríguez,
Youssra Salhi,
Esther Pérez,
Dimitra R. Bakaloudi,
Rafee Talukder,
Belen Caramelo,
Rafael Morales-Barrera,
Astrid De Meulenaere,
Alessandro Rametta,
Andrea Bottelli,
Felix Lefort,
Patrizia Giannatempo,
Christof Vulsteke,
Joan Carles,
Ignacio Duran,
Petros Grivas,
Alfonso Gómez de Liaño,
Debbie G. J. Robbrecht,
Begoña P. Valderrama,
Vincent van der Noort,
Michiel S. van der Heijden
Affiliations
Chantal F. Stockem
Department of Medical Oncology, The Netherlands Cancer Institute
Sarah M. H. Einerhand
Department of surgical oncology (urology), The Netherlands Cancer Institute
Isabel Miras Rodríguez
Department of Medical Oncology, Hospital Universitario Virgen del Rocio
Youssra Salhi
Department of Medical Oncology, Erasmus Medical Center
Esther Pérez
Department of Medical Oncology, Hospital Complex Insular-Materno Infantil
Dimitra R. Bakaloudi
Department of Medicine, Division of Hematology and Oncology, University of Washington
Rafee Talukder
Department of Medicine, Division of Hematology and Oncology, University of Washington
Belen Caramelo
Department of Medical Oncology, Hospital Universitario Marqués de Valdecilla
Rafael Morales-Barrera
Vall d’Hebron Institute of Oncology, Vall d’Hebron University Hospital
Astrid De Meulenaere
Department of Medical Oncology, Integrated Cancer Center, AZ Maria Middelares
Alessandro Rametta
Oncologia Medica Genito-Urinaria, Fondazione IRCCS Istituto Nazionale dei Tumori
Andrea Bottelli
Oncologia Medica Genito-Urinaria, Fondazione IRCCS Istituto Nazionale dei Tumori
Felix Lefort
Department of Medical Oncology, Hôspital Saint André—CHU de Bordeaux
Patrizia Giannatempo
Oncologia Medica Genito-Urinaria, Fondazione IRCCS Istituto Nazionale dei Tumori
Christof Vulsteke
Department of Medical Oncology, Integrated Cancer Center, AZ Maria Middelares
Joan Carles
Vall d’Hebron Institute of Oncology, Vall d’Hebron University Hospital
Ignacio Duran
Department of Medical Oncology, Hospital Universitario Marqués de Valdecilla
Petros Grivas
Department of Medicine, Division of Hematology and Oncology, University of Washington
Alfonso Gómez de Liaño
Department of Medical Oncology, Hospital Complex Insular-Materno Infantil
Debbie G. J. Robbrecht
Department of Medical Oncology, Erasmus Medical Center
Begoña P. Valderrama
Department of Medical Oncology, Hospital Universitario Virgen del Rocio
Vincent van der Noort
Department of Biometrics, The Netherlands Cancer Institute
Michiel S. van der Heijden
Department of Medical Oncology, The Netherlands Cancer Institute
Abstract Background Anti-PD-(L)1 agent are approved as first- and second-line treatment options in advanced urothelial cancer (UC), but information about long-term survival is scarce. There is a need for prognostic factors, as these may help in the decision-making concerning anti-PD-(L)1 in patients with UC. Here, we examined long-term survival following anti-PD-(L)1 in advanced UC and assessed clinical factors for their correlation with survival. Methods We collected data from patients with advanced UC treated with anti-PD-(L)1 between 2013 and 2023. Overall- and progression-free survival (OS, PFS) were determined using the Kaplan-Meier method. Independent variables were analysed by uni- and multivariate Cox regression for their association with OS and PFS. Results Survival analyses included 552 patients. Patient characteristics in our cohort were consistent with those of a typical advanced UC population. After median follow-up of 49 months, five-year OS and PFS rates were 16.0% and 6.9% respectively. The absence of visceral and/or bone metastases and elevated C-reactive protein level, gamma-glutamyltransferase level and neutrophil-to-lymphocyte ratio were identified as favourable prognostic factors for OS. Conclusions A selected subset of patients with advanced UC may experience long-term clinical benefit from anti-PD-(L)1 treatment. We identified prognostic factors that might be used for risk assessment and clinical trial stratification.