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Long-term results of prednisone treatment for the anemia of myelofibrosis.

Abstract
This study has retrospectively analyzed the efficacy of single-agent prednisone, usually given after failure of other therapies, in 30 patients with myelofibrosis (MF) and severe anemia. Initial dose was 0.5-1 mg/kg daily, with tapering to the minimum effective dose in responders. Twelve patients (40%) achieved anemia response according to the revised International Working Group for Myelofibrosis Research and Treatment criteria, after a median time of 1.1 months on treatment. Median response duration was 12.3 months. Patients with constitutional symptoms or > 2% circulating blasts had a trend for a lower response rate. A platelet increase > 50 × 10(9)/L was observed in three out of 11 patients with baseline counts < 100 × 10(9)/L. Median survival from prednisone start was significantly longer in anemia responders (5.0 years, 95% CI = 3.5-6.5, vs 1.5 years, 95% CI = 0.2-2.8; p = 0.002). Prednisone can improve the anemia and thrombocytopenia in selected MF patients after failure to standard therapies.
AuthorsJuan-Carlos Hernández-Boluda, Alejandra Martínez-Trillos, Valentín García-Gutiérrez, Francisca Ferrer-Marín, Blanca Xicoy, Alberto Alvarez-Larrán, Ana Kerguelen, Pere Barba, Montse Gómez, Juan-Carlos Herrera, Juan-Gonzalo Correa, Francisco Cervantes
JournalLeukemia & lymphoma (Leuk Lymphoma) Vol. 57 Issue 1 Pg. 120-4 ( 2016) ISSN: 1029-2403 [Electronic] United States
PMID25944376 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Anti-Inflammatory Agents
  • Immunosuppressive Agents
  • Prednisone
Topics
  • Aged
  • Anemia (diagnosis, drug therapy, etiology)
  • Anti-Inflammatory Agents (administration & dosage, adverse effects, therapeutic use)
  • Bone Marrow (pathology)
  • Erythrocyte Indices
  • Female
  • Humans
  • Immunosuppressive Agents (administration & dosage, adverse effects, therapeutic use)
  • Male
  • Middle Aged
  • Mutation
  • Prednisone (administration & dosage, adverse effects, therapeutic use)
  • Primary Myelofibrosis (complications, diagnosis, genetics)
  • Retrospective Studies
  • Treatment Outcome

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