Scientific Reports (Aug 2024)

Radiotherapy plus pembrolizumab for advanced urothelial carcinoma: results from the ARON-2 real-world study

  • Mimma Rizzo,
  • Andrey Soares,
  • Enrique Grande,
  • Aristotelis Bamias,
  • Ray Manneh Kopp,
  • Edoardo Lenci,
  • Thomas Buttner,
  • Samer Salah,
  • Francesco Grillone,
  • Icaro Thiago de Carvalho,
  • Jose Carlos Tapia,
  • Calogero Gucciardino,
  • Alvaro Pinto,
  • Alessia Mennitto,
  • Halima Abahssain,
  • Pasquale Rescigno,
  • Zin Myint,
  • Hideki Takeshita,
  • Gian Paolo Spinelli,
  • Lazar Popovic,
  • Maria Giuseppa Vitale,
  • Ondrej Fiala,
  • Patrizia Giannatempo,
  • Roubini Zakopoulou,
  • Francesco Carrozza,
  • Francesco Massari,
  • Fernando Sabino Marques Monteiro,
  • Maria Paola Pace,
  • Massimo Giannini,
  • Giandomenico Roviello,
  • Camillo Porta,
  • Nicola Battelli,
  • Ravindran Kanesvaran,
  • Matteo Santoni

DOI
https://doi.org/10.1038/s41598-024-70182-3
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 11

Abstract

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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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