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Radiotherapy plus pembrolizumab for advanced urothelial carcinoma: results from the ARON-2 real-world study.
Rizzo, Mimma; Soares, Andrey; Grande, Enrique; Bamias, Aristotelis; Kopp, Ray Manneh; Lenci, Edoardo; Buttner, Thomas; Salah, Samer; Grillone, Francesco; de Carvalho, Icaro Thiago; Tapia, Jose Carlos; Gucciardino, Calogero; Pinto, Alvaro; Mennitto, Alessia; Abahssain, Halima; Rescigno, Pasquale; Myint, Zin; Takeshita, Hideki; Spinelli, Gian Paolo; Popovic, Lazar; Vitale, Maria Giuseppa; Fiala, Ondrej; Giannatempo, Patrizia; Zakopoulou, Roubini; Carrozza, Francesco; Massari, Francesco; Monteiro, Fernando Sabino Marques; Pace, Maria Paola; Giannini, Massimo; Roviello, Giandomenico; Porta, Camillo; Battelli, Nicola; Kanesvaran, Ravindran; Santoni, Matteo.
Afiliação
  • Rizzo M; Medical Oncology Unit, Azienda Ospedaliero Universitaria Consorziale Policlinico Di Bari, Piazza Giulio Cesare 11, 70124, Bari, Italy. rizzo.mimma@gmail.com.
  • Soares A; Medical Oncology Unit, Hospital Israelita Albert Einstein, São Paulo, SP, Brazil.
  • Grande E; Latin American Cooperative Oncology Group - LACOG, Porto Alegre, Brazil.
  • Bamias A; Department of Medical Oncology, MD Anderson Cancer Center Madrid, Madrid, Spain.
  • Kopp RM; Second Propaedeutic Department of Internal Medicine, Attikon University Hospital, National and Kapodistrian University of Athens, Athens, Greece.
  • Lenci E; Clinical Oncology, Sociedad de Oncología y Hematología del Cesar, Valledupar, Colombia.
  • Buttner T; Medical Oncology Unit, Azienda Ospedaliera Ospedali Riuniti Marche Nord, Pesaro, Italy.
  • Salah S; Department of Urology, University Hospital Bonn (UKB), Bonn, Germany.
  • Grillone F; Department of Medical Oncology, King Hussein Cancer Center, Amman, Jordan.
  • de Carvalho IT; Medical Oncology Unit, Presidio Ospedaliero Pugliese Ciaccio, Azienda Ospedaliera Universitaria "Renato Dulbecco", Catanzaro, Italy.
  • Tapia JC; Radiation Oncology Unit, Hospital Israelita Albert Einstein, São Paulo, SP, Brazil.
  • Gucciardino C; Department of Medical Oncology, Institut d'Investigació Biomèdica Sant Pau, Hospital de La Santa Creu I Sant Pau, Barcelona, Spain.
  • Pinto A; Medical Oncology Unit, Ospedale A. Murri, Fermo, Italy.
  • Mennitto A; Medical Oncology Department, University Hospital La Paz, Madrid, Spain.
  • Abahssain H; Department of Medical Oncology, Azienda Ospedaliera Universitaria "Maggiore Della Carità", Novara, Italy.
  • Rescigno P; Medicine and Pharmacy Faculty, Medical Oncology Unit, National Institute of Oncology, Mohamed V University, Rabat, Morocco.
  • Myint Z; Centre for Cancer, Translational and Clinical Research Institute, Newcastle University, Newcastle Upon Tyne, UK.
  • Takeshita H; Division of Medical Oncology, Markey Cancer Center, University of Kentucky, Lexington, KY, 40536-0293, USA.
  • Spinelli GP; Department of Urology, Saitama Medical Center, Saitama Medical University, Saitama, Japan.
  • Popovic L; Territorial Oncology Operative Complex Unit - Casa Della Salute di Aprilia - ASL Latina, Latina, Italy.
  • Vitale MG; Oncology Institute of Vojvodina, Faculty of Medicine, University Novi Sad, Novi Sad, Serbia.
  • Fiala O; Division of Oncology, Department of Oncology and Hematology, University Hospital of Modena, Modena, Italy.
  • Giannatempo P; Department of Oncology and Radiotherapeutics, Faculty of Medicine and University Hospital in Pilsen, Charles University, Pilsen, Czech Republic.
  • Zakopoulou R; Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
  • Carrozza F; Genitourinary Medical Oncology Department, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.
  • Massari F; Second Propaedeutic Department of Internal Medicine, Attikon University Hospital, National and Kapodistrian University of Athens, Athens, Greece.
  • Monteiro FSM; Oncology Unit, Santa Maria Delle Croci Hospital, Department Oncology and Haematology AUSL, Romagna, Ravenna, Italy.
  • Pace MP; Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria Di Bologna, Bologna, Italy.
  • Giannini M; Oncology and Hematology Department, Hospital Sírio Libanês, Brasília, Federal District, Brazil.
  • Roviello G; Radiation Oncology Unit, Macerata Hospital, Macerata, Italy.
  • Porta C; Radiation Oncology Unit, Macerata Hospital, Macerata, Italy.
  • Battelli N; Department of Health Sciences, Section of Clinical Pharmacology and Oncology, University of Florence, Florence, Italy.
  • Kanesvaran R; Medical Oncology Unit, Azienda Ospedaliero Universitaria Consorziale Policlinico Di Bari, Piazza Giulio Cesare 11, 70124, Bari, Italy.
  • Santoni M; Interdisciplinary Department of Medicine, University of Bari "Aldo Moro", Bari, Italy.
Sci Rep ; 14(1): 19802, 2024 08 27.
Article em En | MEDLINE | ID: mdl-39187558
ABSTRACT
The addition of metastasis-directed radiotherapy (MDRT) to immunotherapy in patients with advanced urothelial carcinoma (aUC) has shown promising results. We report the real-world data from the ARON-2 study (NCT05290038) on the impact of conventional (CRT) or stereotactic body radiotherapy (SBRT) on the outcome of aUC patients receiving pembrolizumab after platinum-based-chemotherapy. Medical records of 837 patients were reviewed from 60 institutions in 20 countries. Two hundred and sixty-two patients (31%) received radiotherapy (cohort A), of whom 193 (23%) received CRT and 69 (8%) received SBRT. Patients were assessed for overall survival (OS), progression-free survival (PFS), and overall response rate (ORR). Univariate and multivariate analyses were used to explore the association of variables of interest with OS and PFS. With a median follow-up of 22.7 months, the median OS was 10.2 months, 6.8 months and 16.0 months in no RT, CRT and SBRT subgroups (p = 0.005), with an 1y-OS rates of 47%, 34% and 61%, respectively (p < 0.001). The 1y-OS rate in the SBRT subgroup were significantly higher for both lower (63%) and upper tract UC (68%), for pure urothelial histology (63%) and variant histologies (58%), and for patients with bone (40%) and lymph-node metastases (61%). Median PFS was 4.8 months, 9.6 months and 5.8 months in the CRT, SBRT and no RT subgroups, respectively (p = 0.060). The 1y-PFS rate was significantly higher (48%) in the SBRT population and was confirmed in all patient subsets. The difference in terms of ORR was in favour of SBRT. Our real-world analysis showed that the use of SBRT/pembrolizumab combination may play a role in a subset of aUC patients to increase disease control and possibly overall survival.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anticorpos Monoclonais Humanizados Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Sci Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anticorpos Monoclonais Humanizados Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Sci Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália