Cancer Treatment and Research Communications (Jan 2025)

The prognostic value of the haemoglobin/red cell distribution width ratio in a cohort of pre-treated patients with renal cell carcinoma receiving nivolumab

  • Giulia Claire Giudice,
  • Sara Elena Rebuzzi,
  • Giulia Mazzaschi,
  • Federica Pecci,
  • Michele Maffezzoli,
  • Alessandro Acunzo,
  • Letizia Gnetti,
  • Enrico Maria Silini,
  • Giuseppe Caruso,
  • Elena Rapacchi,
  • Pasquale Rescigno,
  • Giuseppe Fornarini,
  • Giuseppe Luigi Banna,
  • Sebastiano Buti

DOI
https://doi.org/10.1016/j.ctarc.2025.100927
Journal volume & issue
Vol. 43
p. 100927

Abstract

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Background: Metastatic renal cell carcinoma (mRCC) has a dismal prognosis. Effective prognostic and predictive factors are needed. A higher haemoglobin (Hb) / red cell distribution width (RDW) ratio is known to be related to better outcomes. Here we evaluated the prognostic value of the Hb/RDW ratio in pre-treated mRCC patients receiving nivolumab. Material and methods: This is a sub-analysis of the retrospective Meet-URO 15 study, on pre-treated patients with mRCC, receiving nivolumab. The first objective was to investigate the prognostic role of Hb/RDW ratio, in terms of overall survival (OS) and progression-free survival (PFS). Results: 356 were included in the present analysis. Patients were mainly males with a median age of 63 years. We classified patients in high and low Hb/RDW ratio, according to two different cut-offs: 0.9frequently used in literature, and 0.7, result of the time-dependent AUC analysis.. Median OS and PFS were 22.3 months (95 %CI 19.4–29.0) and 5.6 months (95 %CI 4.74.–7.53), respectively. At univariable analysis, higher Hb/RDW ratio was related to longer OS (p < 0.001) and PFS (p = 0.011); the multivariable model confirmed only the association between a Hb/RDW ratio ≥ 0.7 and better OS. Conclusions: The Hb/RDW ratio is a manageable and practical prognostic tool in patients with cancer; its prognostic value for OS was confirmed in pre-treated mRCC patients, receiving nivolumab, only using a cut-off value derived from a time-dependent AUC.

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