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Real-world evidences on adjuvant Pembrolizumab for renal cell carcinoma: results from the multicenter real-world ARON-1 study

  • Ray Manneh Kopp
  • , Francesco Massari
  • , Enrique Grande
  • , Timothy J. Schieber
  • , Yüksel Ürün
  • , Jindřich Kopecký
  • , Javier Molina-Cerrillo
  • , Umberto Basso
  • , Jakub Kucharz
  • , Thomas Büttner
  • , Renate Pichler
  • , Ondrej Fiala
  • , Zin W. Myint
  • , Luca Galli
  • , Tomas Buchler
  • , Mimma Rizzo
  • , Hatice Bolek
  • , Maria T. Bourlon
  • , Vincenza Conteduca
  • , Alvaro Pinto
  • Alessandro Rizzo, Matteo Rosellini, Giandomenico Roviello, Anca Zgura, Veronica Mollica, Antonia Partl, Ahmet Yildirim, Umut Akova, Sebastiano Buti, Fernando Sabino Marques Monteiro, Andrey Soares, Camillo Porta, Mehmet Asim Bilen, Haoran Li, Matteo Santoni

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Background: Pembrolizumab has demonstrated efficacy in improving disease-free survival (DFS) and overall survival (OS) as adjuvant therapy in clear cell renal cell carcinoma (ccRCC) at a higher risk of recurrence. However, real-world data on its effectiveness and safety remain limited. This study evaluates DFS, OS and severe adverse events (SAEs) associated with adjuvant pembrolizumab in a multicenter international cohort. Methods: This retrospective analysis included 311 ccRCC patients treated with adjuvant pembrolizumab across 40 hospitals in 12 countries from the ARON-1 dataset. Eligible patients had histologically confirmed ccRCC with high relapse risk and received up to 17 cycles of pembrolizumab. The primary objective was DFS, with OS and safety as secondary objectives. Kaplan–Meier survival estimates, Cox proportional hazards models and log-rank tests were used for statistical analysis. Results: At a median follow-up of 15.4-month, 2-year OS and DFS rates were 95% and 69%, respectively. Recurrence occurred in 20% of patients, primarily in the lungs (11%) and bones (5%). DFS was significantly impaired in patients < 65 years (HR 2.14, p = 0.005), N1 disease (HR 5.42, p = 0.004) and sarcomatoid dedifferentiation (HR 2.54, p = 0.007). SAEs led to 19% treatment discontinuation, with colitis (4%), hypertransaminasemia (4%) and nephritis (3%) as the most common events. The study’s retrospective nature and short follow-up limit long-term outcome assessments. Conclusions: This large real-world study confirms pembrolizumab’s effectiveness and manageable safety profile in the adjuvant setting for intermediate-high and high-risk ccRCC. Further research is needed to refine patient selection strategies and evaluate long-term outcomes.

Original languageEnglish
Article number374
JournalCancer Immunology, Immunotherapy
Volume74
Issue number12
DOIs
StatePublished - Dec 2025

Bibliographical note

Publisher Copyright:
© The Author(s) 2025.

Funding

Open access funding provided by Alma Mater Studiorum - Università di Bologna within the CRUI-CARE Agreement. The research leading to these results has received funding from the European Union—Next Generation EU through the Italian Ministry of University and Research under PNRR-M4C2-I1.3 Project PE_00000019 ‘‘HEAL ITALIA’’ to Francesco Massari (Spoke 8 University of Bologna), CUP J33C22002920006. The views and opinions expressed are those of the authors only and do not necessarily reflect those of the European Union or the European Commission. Neither the European Union nor the European Commission can be held responsible for them.

FundersFunder number
Alma Mater Studiorum -Universita' di Bologna
European Commission
Ministero dell’Istruzione, dell’Università e della RicercaPE_00000019
Università di BolognaCUP J33C22002920006

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • ARON-1
    • Adjuvant therapy
    • Immune checkpoint inhibitor
    • Pembrolizumab
    • Real-world data
    • Renal cell carcinoma

    ASJC Scopus subject areas

    • Immunology and Allergy
    • Immunology
    • Oncology
    • Cancer Research

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