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Effect of rosuvastatin on risk markers for venous thromboembolism in cancer.
Ades, S; Douce, D; Holmes, C E; Cory, S; Prior, S; Butenas, S; Callas, P; Cushman, M.
Affiliation
  • Ades S; Department of Medicine, Larner College of Medicine, University of Vermont, Burlington, VT, USA.
  • Douce D; Department of Medicine, Larner College of Medicine, University of Vermont, Burlington, VT, USA.
  • Holmes CE; Department of Medicine, Larner College of Medicine, University of Vermont, Burlington, VT, USA.
  • Cory S; Department of Graduate Entry Medicine, Royal College of Surgeons, Dublin, Ireland.
  • Prior S; Department of Medicine, Larner College of Medicine, University of Vermont, Burlington, VT, USA.
  • Butenas S; Department of Biochemistry, Larner College of Medicine, University of Vermont, Colchester, VT, USA.
  • Callas P; Department of Medical Biostatistics, University of Vermont, Burlington, VT, USA.
  • Cushman M; Department of Medicine, Larner College of Medicine, University of Vermont, Burlington, VT, USA.
J Thromb Haemost ; 16(6): 1099-1106, 2018 06.
Article in En | MEDLINE | ID: mdl-29575637
ABSTRACT
Essentials Statins lower venous thromboembolism risk in general but have not been studied in cancer patients. We completed a randomized trial of rosuvastatin vs. placebo among cancer patients on chemotherapy. Rosuvastatin did not significantly lower prothrombotic biomarkers including D-dimer. The role of statins in venous thrombosis prevention in cancer patients remains unknown.

SUMMARY:

Background Statin therapy is associated with lower risk of venous thromboembolism (VTE) but has not been prospectively evaluated in patients with advanced cancer. Objectives We determined if statin administration in this high-risk population reduces the risk of VTE, based on established and emerging biomarkers. Patients/Methods This double-blind, crossover, randomized controlled trial among patients with advanced cancer receiving systemic therapy allocated participants to rosuvastatin 20 mg daily or placebo for 3-4 weeks prior to crossover to the alternative therapy, with a 3-5-week washout. D-dimer, C-reactive protein (CRP), soluble (s)P-selectin, factor VIII (FVIII), thrombin generation and exploratory biomarkers focusing on endogenous thrombin potential, including tissue factor (TF), activated factor IX (FIXa) and activated factor XI (FXIa), were measured at the start and end of both treatment periods. The primary outcome was change in D-dimer with rosuvastatin compared with placebo. Results Of 38 enrolled participants, 24 (63%) completed the study. Rosuvastatin did not cause statistically significant changes in D-dimer levels or any other biomarker. CRP levels decreased by 40%; 4.3 mg L-1 (95% confidence interval, -11.0 to +2.5 mg L-1 ) compared with placebo. In post-hoc analysis, participants who received rosuvastatin initially during their first line of treatment had a 13% decrease in D-dimer. Circulating TF, FIXa and FXIa were detected in 26%, 68% and 71% of cancer patients despite not being found in healthy individuals. Conclusions Rosuvastatin did not cause favorable changes in biomarkers of VTE risk in advanced cancer patients receiving chemotherapy. The role of statin therapy as thromboprophylaxis in the cancer population remains uncertain.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Fibrin Fibrinogen Degradation Products / Hydroxymethylglutaryl-CoA Reductase Inhibitors / Venous Thromboembolism / Fibrinolytic Agents / Rosuvastatin Calcium / Neoplasms / Antineoplastic Agents Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Risk_factors_studies Limits: Aged80 Country/Region as subject: America do norte Language: En Journal: J Thromb Haemost Journal subject: HEMATOLOGIA Year: 2018 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Fibrin Fibrinogen Degradation Products / Hydroxymethylglutaryl-CoA Reductase Inhibitors / Venous Thromboembolism / Fibrinolytic Agents / Rosuvastatin Calcium / Neoplasms / Antineoplastic Agents Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Risk_factors_studies Limits: Aged80 Country/Region as subject: America do norte Language: En Journal: J Thromb Haemost Journal subject: HEMATOLOGIA Year: 2018 Type: Article Affiliation country: United States