Frontiers in Oncology (Feb 2024)

Time to strategy failure and treatment beyond progression in pretreated metastatic renal cell carcinoma patients receiving nivolumab: post-hoc analysis of the Meet-URO 15 study

  • Veronica Murianni,
  • Alessio Signori,
  • Sebastiano Buti,
  • Sebastiano Buti,
  • Sara Elena Rebuzzi,
  • Sara Elena Rebuzzi,
  • Davide Bimbatti,
  • Ugo De Giorgi,
  • Silvia Chiellino,
  • Luca Galli,
  • Paolo Andrea Zucali,
  • Cristina Masini,
  • Emanuele Naglieri,
  • Giuseppe Procopio,
  • Michele Milella,
  • Lucia Fratino,
  • Cinzia Baldessari,
  • Riccardo Ricotta,
  • Veronica Mollica,
  • Mariella Sorarù,
  • Marianna Tudini,
  • Veronica Prati,
  • Andrea Malgeri,
  • Francesco Atzori,
  • Marilena Di Napoli,
  • Orazio Caffo,
  • Massimiliano Spada,
  • Franco Morelli,
  • Giuseppe Prati,
  • Franco Nolè,
  • Francesca Vignani,
  • Alessia Cavo,
  • Helga Lipari,
  • Giandomenico Roviello,
  • Fabio Catalano,
  • Alessandra Damassi,
  • Malvina Cremante,
  • Pasquale Rescigno,
  • Pasquale Rescigno,
  • Giuseppe Fornarini,
  • Giuseppe Luigi Banna,
  • Giuseppe Luigi Banna

DOI
https://doi.org/10.3389/fonc.2024.1307635
Journal volume & issue
Vol. 14

Abstract

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BackgroundImmunotherapies exhibit peculiar cancer response patterns in contrast to chemotherapy and targeted therapy. Some patients experience disease response after initial progression or durable responses after treatment interruption. In clinical practice, immune checkpoint inhibitors may be continued after radiological progression if clinical benefit is observed. As a result, estimating progression-free survival (PFS) based on the first disease progression may not accurately reflect the actual benefit of immunotherapy.MethodsThe Meet-URO 15 study was a multicenter retrospective analysis of 571 pretreated metastatic renal cell carcinoma (mRCC) patients receiving nivolumab. Time to strategy failure (TSF) was defined as the interval from the start of immunotherapy to definitive disease progression or death. This post-hoc analysis compared TSF to PFS and assess the response and survival outcomes between patients treatated beyond progression (TBP) and non-TBP. Moreover, we evaluated the prognostic accuracy of the Meet-URO score versus the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) score based on TSF and PFS.ResultsOverall, 571 mRCC patients were included in the analysis. Median TSF was 8.6 months (95% CI: 7.0 – 10.1), while mPFS was 7.0 months (95% CI: 5.7 – 8.5). TBP patients (N = 93) had significantly longer TSF (16.3 vs 5.5 months; p < 0.001) and overall survival (OS) (34.8 vs 17.9 months; p < 0.001) but similar PFS compared to non-TBP patients. In TBP patients, a median delay of 9.6 months (range: 6.7-16.3) from the first to the definitive disease progression was observed, whereas non-TBP patients had overlapped median TSF and PFS (5.5 months). Moreover, TBP patients had a trend toward a higher overall response rate (33.3% vs 24.3%; p = 0.075) and disease control rate (61.3% vs 55.5%; p = 0.31). Finally, in the whole population the Meet-URO score outperformed the IMDC score in predicting both TSF (c-index: 0.63 vs 0.59) and PFS (0.62 vs 0.59).ConclusionWe found a 2-month difference between mTSF and mPFS in mRCC patients receiving nivolumab. However, TBP patients had better outcomes, including significantly longer TSF and OS than non-TBP patients. The Meet-URO score is a reliable predictor of TSF and PFS.

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