Cardiovascular events and intensity of treatment in polycythemia vera.
Abstract
Background Current treatment recommendations for patients with polycythemia vera call for maintaining a hematocrit of less than 45%, but this therapeutic strategy has not been tested in a randomized clinical trial. Methods We randomly assigned 365 adults with JAK2-positive polycythemia vera who were being treated with phlebotomy, hydroxyurea, or both to receive either more intensive treatment (target hematocrit, <45%) (low-hematocrit group) or less intensive treatment (target hematocrit, 45 to 50%) (high-hematocrit group). The primary composite end point was the time until death from cardiovascular causes or major thrombotic events. The secondary end points were cardiovascular events, cardiovascular hospitalizations, incidence of cancer, progression to myelofibrosis, myelodysplasia or leukemic transformation, and hemorrhage. An intention-to-treat analysis was performed. Results After a median follow-up of 31 months, the primary end point was recorded in 5 of 182 patients in the low-hematocrit group (2.7%) and 18 of 183 patients in the highhematocrit group (9.8%) (hazard ratio in the high-hematocrit group, 3.91; 95% confidence interval [CI], 1.45 to 10.53; P=0.007). The primary end point plus superficial-vein thrombosis occurred in 4.4% of patients in the low-hematocrit group, as compared with 10.9% in the high-hematocrit group (hazard ratio, 2.69; 95% CI, 1.19 to 6.12; P=0.02). Progression to myelofibrosis, myelodysplasia or leukemic transformation, and bleeding were observed in 6, 2, and 2 patients, respectively, in the low-hematocrit group, as compared with 2, 1, and 5 patients, respectively, in the high-hematocrit group. There was no significant between-group difference in the rate of adverse events. Conclusions In patients with polycythemia vera, those with a hematocrit target of less than 45% had a significantly lower rate of cardiovascular death and major thrombosis than did those with a hematocrit target of 45 to 50%. (Funded by the Italian Medicines Agency and others;
Autore Pugliese
Tutti gli autori
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D'ANGELO A.;GIANNOTTA A.;MAZZONE A.M.;SCARANO A.M.;GUIDO C.D.;DOGARU E.C.;ROSSI E.;ALBANO F.;GUARAGNA G.;SPECCHIA G.;MALERBA L.;QUARTA R.M.G.;SANTINI S.;DE STEFANO V.
Titolo volume/Rivista
Non Disponibile
Anno di pubblicazione
2013
ISSN
0028-4793
ISBN
Non Disponibile
Numero di citazioni Wos
277
Ultimo Aggiornamento Citazioni
Non Disponibile
Numero di citazioni Scopus
290
Ultimo Aggiornamento Citazioni
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Settori ERC
Non Disponibile
Codici ASJC
Non Disponibile
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