Cancers (Jul 2024)

Prognostic Implications of Blood Immune-Cell Composition in Metastatic Castration-Resistant Prostate Cancer

  • Enrique Perez-Navarro,
  • Vincenza Conteduca,
  • Juan M. Funes,
  • Jose I. Dominguez,
  • Miguel Martin-Serrano,
  • Paolo Cremaschi,
  • Maria Piedad Fernandez-Perez,
  • Teresa Alonso Gordoa,
  • Albert Font,
  • Sergio Vázquez-Estévez,
  • Aránzazu González-del-Alba,
  • Daniel Wetterskog,
  • Begona Mellado,
  • Ovidio Fernandez-Calvo,
  • María José Méndez-Vidal,
  • Miguel Angel Climent,
  • Ignacio Duran,
  • Enrique Gallardo,
  • Angel Rodriguez Sanchez,
  • Carmen Santander,
  • Maria Isabel Sáez,
  • Javier Puente,
  • Julian Tudela,
  • Cecilia Marinas,
  • María Jose López-Andreo,
  • Daniel Castellano,
  • Gerhardt Attard,
  • Enrique Grande,
  • Antonio Rosino,
  • Juan A. Botia,
  • Jose Palma-Mendez,
  • Ugo De Giorgi,
  • Enrique Gonzalez-Billalabeitia

DOI
https://doi.org/10.3390/cancers16142535
Journal volume & issue
Vol. 16, no. 14
p. 2535

Abstract

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The prognosis for patients with metastatic castration-resistant prostate cancer (mCRPC) varies, being influenced by blood-related factors such as transcriptional profiling and immune cell ratios. We aimed to address the contribution of distinct whole blood immune cell components to the prognosis of these patients. This study analyzed pre-treatment blood samples from 152 chemotherapy-naive mCRPC patients participating in a phase 2 clinical trial (NCT02288936) and a validation cohort. We used CIBERSORT-X to quantify 22 immune cell types and assessed their prognostic significance using Kaplan–Meier and Cox regression analyses. Reduced CD8 T-cell proportions and elevated monocyte levels were substantially connected with a worse survival. High monocyte counts correlated with a median survival of 32.2 months versus 40.3 months for lower counts (HR: 1.96, 95% CI 1.11–3.45). Low CD8 T-cell levels were associated with a median survival of 31.8 months compared to 40.3 months for higher levels (HR: 1.97, 95% CI 1.11–3.5). These findings were consistent in both the trial and validation cohorts. Multivariate analysis further confirmed the independent prognostic value of CD8 T-cell counts. This study highlights the prognostic implications of specific blood immune cells, suggesting they could serve as biomarkers in mCRPC patient management and should be further explored in clinical trials.

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