Javier Gavira

Dr. Javier Gavira

orcid

Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 March 2025 in European Journal of Cancer
Verified
Journal Article
Closed access
JGJavier Gavira
Javier Gavira
EAEdouard Auclin
Edouard Auclin
MRMacarena Rey-Cardenas
Macarena Rey-Cardenas
PRPritha Roy
Pritha Roy
JTJose C. Tapia
Jose C. Tapia
RFRonan Flippot
Ronan Flippot

2 February 2024 in Clinical Genitourinary Cancer
Verified
Journal Article
Closed access
JTJose C. Tapia
Jose C. Tapia
FBFreya Bosma
Freya Bosma
JGJavier Gavira
Javier Gavira
SSSofia Sanchez
Sofia Sanchez
MMMaria Alejandra Molina
Maria Alejandra Molina
PMPablo p maroto Maroto
Pablo p maroto Maroto

15 April 2022 in International Journal of Cancer
Verified
Journal Article
Closed access
PDF file
JTJose C. Tapia
Jose C. Tapia
JGJavier Gavira
Javier Gavira
ALAssumpció López
Assumpció López
LLLaia Llobera
Laia Llobera
OPOna Pallise
Ona Pallise
MMMargarita Majem
Margarita Majem

26 August 2024 in Cancers
Verified
Journal Article
Open access
PDF file
ESElia Seguí
Elia Seguí
JTJuan Torres
Juan Torres
EAEdouard Auclin
Edouard Auclin
DCDavid Casadevall
David Casadevall
SCSara Peiro Carmona
Sara Peiro Carmona
LMLaura Mezquita
Laura Mezquita
Purpose: Inflammation and neutrophils play a central role in both COVID-19 disease and cancer. We aimed to assess the impact of pre-existing tumor-related inflammation on COVID-19 outcomes in patients with cancer and to elucidate the role of circulating neutrophil subpopulations. Methods: We conducted a multicenter retrospective analysis of 524 patients with cancer and SARS-CoV-2 infection, assessing the relationship between clinical outcomes and circulating inflammatory biomarkers collected before and during COVID-19 infection. Additionally, a single-center prospective cohort study provided data for an exploratory analysis, assessing the immunophenotype of circulating neutrophils and inflammatory cytokines. The primary endpoints were 30-day mortality and the severity of COVID-19 disease. Results: Prior to COVID-19, 25% of patients with cancer exhibited elevated dNLR, which increased to 55% at the time of COVID-19 diagnosis. We developed the FLARE score, incorporating both tumor- and infection-induced inflammation, which categorized patients into four prognostic groups. The poor prognostic group had a 30-day mortality rate of 68%, significantly higher than the 23% in the favorable group (p < 0.0001). This score proved to be an independent predictor of early mortality. This prospective analysis revealed a shift towards immature forms of neutrophils and higher IL-6 levels in patients with cancer and severe COVID-19 infection. Conclusions: A pre-existing tumor-induced pro-inflammatory state significantly impacts COVID-19 outcomes in patients with cancer. The FLARE score, derived from circulating inflammatory markers, emerges as an easy-to-use, globally accessible, effective tool for clinicians to identify patients with cancer at heightened risk of severe COVID-19 complications and early mortality who might benefit most from immediate and intensive treatment strategies. Furthermore, our findings underscore the significance of immature neutrophils in the progression of COVID-19 in patients with cancer, advocating for further investigation into how these cells contribute to both cancer and COVID-19 disease.

9 May 2024 in Clinical and Translational Oncology
Verified
Journal Article
Closed access
PDF file
JGJavier Gavira
Javier Gavira
JTJose C. Tapia
Jose C. Tapia
ARAlejandra Romano
Alejandra Romano
GAGeorgia Anguera
Georgia Anguera
MAMaría Aguado
María Aguado
PMPablo p maroto Maroto
Pablo p maroto Maroto