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Association between elevated white blood cell counts and thrombotic events in polycythemia vera: analysis from REVEAL.
Gerds, Aaron T; Mesa, Ruben; Burke, John M; Grunwald, Michael R; Stein, Brady L; Squier, Peg; Yu, Jingbo; Hamer-Maansson, J E; Oh, Stephen T.
Afiliação
  • Gerds AT; Cleveland Clinic Taussig Cancer Institute, Cleveland, OH.
  • Mesa R; UT Health San Antonio MD Anderson Cancer Center, San Antonio, TX.
  • Burke JM; Rocky Mountain Cancer Centers, Aurora, CO.
  • Grunwald MR; Levine Cancer Institute, Atrium Health, Charlotte, NC.
  • Stein BL; Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Squier P; Incyte Corporation, Wilmington, DE.
  • Yu J; Incyte Corporation, Wilmington, DE.
  • Hamer-Maansson JE; Incyte Corporation, Wilmington, DE.
  • Oh ST; Washington University School of Medicine, St. Louis, MO.
Blood ; 143(16): 1646-1655, 2024 Apr 18.
Article em En | MEDLINE | ID: mdl-38142448
ABSTRACT
ABSTRACT Polycythemia vera (PV) is a myeloproliferative neoplasm characterized by clonal proliferation of hematopoietic progenitor cells and is associated with an increased risk of thrombotic events (TEs). Established risk factors for TEs in patients with PV include advanced age, TE history, and elevated hematocrit. Although an association of TE with elevated white blood cell (WBC) counts has been suggested by retrospective studies, this relationship needs further validation. The prospective observational study of patients with polycythemia vera in US clinical practices (REVEAL) study collected prospective clinical data from 2510 patients with PV with a median follow-up of 44.7 months (range, 2-59 months) from enrollment. Using time-dependent covariate Cox proportional hazards models, blood counts were individually modeled with sex, age, disease duration, TE history at enrollment (baseline covariates), and treatment (time-dependent covariate). Analysis of 2271 participants identified 142 TEs in 106 patients. Significant associations with initial TE occurrence during the study period were observed for hematocrit level >45% (hazard ratio [HR], 1.84; 95% confidence interval [95% CI], 1.234-2.749; P = .0028) and WBCs >11 × 109/L (HR, 2.35; 95% CI, 1.598-3.465; P < .0001). Elevated WBC count was significantly associated with initial TE occurrence in both low-risk and high-risk PV. When hematocrit was controlled at ≤45%, WBC count >12 × 109/L was significantly associated with TE occurrence (HR, 1.95; 95% CI, 1.066-3.554; P = .0300). The results support incorporation of WBC count into PV risk stratification and studies of treatment strategies, and indicate the importance of controlling both hematocrit and WBC count in disease management. This trial was registered at www.clinicaltrials.gov as #NCT02252159.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Policitemia Vera / Trombose Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Policitemia Vera / Trombose Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article