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Biomarker-enhanced cardiovascular risk prediction in patients with cancer: a prospective cohort study.
Kraler, Simon; Liberale, Luca; Nopp, Stephan; Englisch, Cornelia; Grilz, Ella; Lapikova-Bryhinska, Tetiana; Akhmedov, Alexander; Carbone, Federico; Ramoni, Davide; Tirandi, Amedeo; Scuricini, Alessandro; Isoppo, Simone; Tortorella, Curzia; La Rosa, Federica; Michelauz, Cristina; Frè, Federica; Gavoci, Aurora; Lisa, Anna; Suter, Thomas M; von Eckardstein, Arnold; Wenzl, Florian A; Pabinger, Ingrid; Lüscher, Thomas F; Montecucco, Fabrizio; Ay, Cihan; Moik, Florian.
Afiliación
  • Kraler S; Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland; Department of Internal Medicine, Cantonal Hospital Baden, Baden, Switzerland. Electronic address: https://twitter.com/KralerSimon.
  • Liberale L; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, Italy; IRCCS Ospedale Policlinico San Martino Genoa - Italian Cardiovascular Network, Genoa, Italy. Electronic address: https://twitter.com/liberale_luca.
  • Nopp S; Department of Medicine I, Clinical Division of Haematology and Haemostaseology, Comprehensive Cancer Center Vienna, Medical University of Vienna, Vienna, Austria.
  • Englisch C; Department of Medicine I, Clinical Division of Haematology and Haemostaseology, Comprehensive Cancer Center Vienna, Medical University of Vienna, Vienna, Austria.
  • Grilz E; Department of Medicine I, Clinical Division of Haematology and Haemostaseology, Comprehensive Cancer Center Vienna, Medical University of Vienna, Vienna, Austria.
  • Lapikova-Bryhinska T; Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.
  • Akhmedov A; Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland.
  • Carbone F; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, Italy; IRCCS Ospedale Policlinico San Martino Genoa - Italian Cardiovascular Network, Genoa, Italy. Electronic address: https://twitter.com/CarboneF82.
  • Ramoni D; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, Italy.
  • Tirandi A; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, Italy.
  • Scuricini A; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, Italy.
  • Isoppo S; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, Italy.
  • Tortorella C; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, Italy.
  • La Rosa F; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, Italy.
  • Michelauz C; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, Italy.
  • Frè F; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, Italy.
  • Gavoci A; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, Italy.
  • Lisa A; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, Italy.
  • Suter TM; Lindenhofgruppe, Bern and Department of Cardiology, Bern University Hospital, University of Bern, Bern, Switzerland.
  • von Eckardstein A; Institute of Clinical Chemistry, University Hospital of Zurich, Zurich, Switzerland.
  • Wenzl FA; Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland. Electronic address: https://twitter.com/wenzl_florian.
  • Pabinger I; Department of Medicine I, Clinical Division of Haematology and Haemostaseology, Comprehensive Cancer Center Vienna, Medical University of Vienna, Vienna, Austria.
  • Lüscher TF; Center for Molecular Cardiology, University of Zurich, Schlieren, Switzerland; Royal Brompton and Harefield Hospitals and Imperial College, London, United Kingdom; School of Cardiovascular Medicine and Sciences, Kings College London, London, United Kingdom. Electronic address: https://twitter.com/To
  • Montecucco F; First Clinic of Internal Medicine, Department of Internal Medicine, University of Genoa, Genoa, Italy; IRCCS Ospedale Policlinico San Martino Genoa - Italian Cardiovascular Network, Genoa, Italy.
  • Ay C; Department of Medicine I, Clinical Division of Haematology and Haemostaseology, Comprehensive Cancer Center Vienna, Medical University of Vienna, Vienna, Austria. Electronic address: cihan.ay@meduniwien.ac.at.
  • Moik F; Department of Medicine I, Clinical Division of Haematology and Haemostaseology, Comprehensive Cancer Center Vienna, Medical University of Vienna, Vienna, Austria; Department of Internal Medicine, Division of Oncology, Medical University of Graz, Graz, Austria. Electronic address: https://twitter.com
J Thromb Haemost ; 2024 Aug 29.
Article en En | MEDLINE | ID: mdl-39223063
ABSTRACT

BACKGROUND:

Continuously improving cancer-specific survival puts a growing proportion of cancer patients at risk of major adverse cardiovascular events (MACE), but tailored tools for cardiovascular risk prediction remain unavailable.

OBJECTIVES:

To assess a broad panel of cardiovascular biomarkers and risk factors for the prediction of MACE and cardiovascular death in cancer patients.

METHODS:

In total, 2192 patients with newly diagnosed or recurrent cancer were followed prospectively for the occurrence of 2-year MACE and 5-year cardiovascular death. Univariable and multivariable risk models were fit to assess independent associations of cardiovascular risk factors and biomarkers with adverse outcomes, and a risk score was developed.

RESULTS:

Traditional cardiovascular risk factors and selected cancer types were linked to higher MACE risk. While levels of Lp(a), CRP, and GDF-15 did not associate with MACE, levels of ICAM-1, P-/E-/L-selectins, and NT-proBNP were independently linked to 2-year MACE risk. A clinical risk score was derived, assigning +1 point for male sex, smoking, and age of ≥60 years and +2 points for atherosclerotic disease, yielding a bootstrapped C-statistic of 0.76 (95% CI 0.71-0.81) for the prediction of 2-year MACE. Implementation of biomarker data conferred improved performance (0.83, 95% CI 0.78-0.88), with a simplified model showing similar performance (0.80, 95% CI 0.74-0.86). The biomarker-enhanced and simplified prediction models achieved a C-statistic of 0.82 (95% CI 0.71-0.93) and 0.74 (95% CI 0.64-0.83) for the prediction of 5-year cardiovascular death.

CONCLUSION:

Biomarker-enhanced risk prediction strategies allow the identification of cancer patients at high risk of MACE and cardiovascular death. While external validation studies are ongoing, this first-of-its-kind risk score may provide the basis for personalized cardiovascular risk assessment across cancer entities.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Thromb Haemost Asunto de la revista: HEMATOLOGIA Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Thromb Haemost Asunto de la revista: HEMATOLOGIA Año: 2024 Tipo del documento: Article