Lenalidomide therapy in myelofibrosis with myeloid metaplasia

Blood. 2006 Aug 15;108(4):1158-64. doi: 10.1182/blood-2006-02-004572. Epub 2006 Apr 11.

Abstract

We present results of 2 similarly designed but separate phase 2 studies involving single-agent lenalidomide (CC-5013, Revlimid) in a total of 68 patients with symptomatic myelofibrosis with myeloid metaplasia (MMM). Protocol treatment consisted of oral lenalidomide at 10 mg/d (5 mg/d if baseline platelet count < 100 x 10(9)/L) for 3 to 4 months with a plan to continue treatment for either 3 or 24 additional months, in case of response. Overall response rates were 22% for anemia, 33% for splenomegaly, and 50% for thrombocytopenia. Response in anemia was deemed impressive in 8 patients whose hemoglobin level normalized from a baseline of either transfusion dependency or hemoglobin level lower than 100 g/L. Additional treatment effects in these patients included resolution of leukoerythroblastosis (4 patients), a decrease in medullary fibrosis and angiogenesis (2 patients), and del(5)(q13q33) cytogenetic remission accompanied by a reduction in JAK2(V617F) mutation burden (1 patient). Grade 3 or 4 adverse events included neutropenia (31%) and thrombocytopenia (19%). We conclude that lenalidomide engenders an intriguing treatment activity in a subset of patients with MMM that includes an unprecedented effect on peripheral blood and bone marrow abnormalities.

Publication types

  • Clinical Trial, Phase II
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Adult
  • Aged
  • Anemia / blood
  • Anemia / complications
  • Anemia / drug therapy
  • Anemia / genetics
  • Anemia / pathology
  • Anemia, Myelophthisic / blood
  • Anemia, Myelophthisic / complications
  • Anemia, Myelophthisic / drug therapy
  • Anemia, Myelophthisic / genetics
  • Anemia, Myelophthisic / pathology
  • Female
  • Hemoglobins / analysis
  • Humans
  • Janus Kinase 2
  • Lenalidomide
  • Male
  • Neovascularization, Pathologic / blood
  • Neovascularization, Pathologic / complications
  • Neovascularization, Pathologic / drug therapy
  • Neovascularization, Pathologic / genetics
  • Neovascularization, Pathologic / pathology
  • Neutropenia / blood
  • Neutropenia / chemically induced
  • Neutropenia / genetics
  • Neutropenia / pathology
  • Platelet Count
  • Point Mutation
  • Primary Myelofibrosis / blood
  • Primary Myelofibrosis / complications
  • Primary Myelofibrosis / drug therapy*
  • Primary Myelofibrosis / genetics
  • Primary Myelofibrosis / pathology
  • Protein-Tyrosine Kinases / genetics
  • Proto-Oncogene Proteins / genetics
  • Remission Induction
  • Sequence Deletion
  • Splenomegaly / blood
  • Splenomegaly / complications
  • Splenomegaly / drug therapy
  • Splenomegaly / genetics
  • Splenomegaly / pathology
  • Thalidomide / administration & dosage
  • Thalidomide / adverse effects
  • Thalidomide / analogs & derivatives*
  • Thrombocytopenia / blood
  • Thrombocytopenia / chemically induced
  • Thrombocytopenia / drug therapy
  • Thrombocytopenia / genetics
  • Thrombocytopenia / pathology
  • Time Factors

Substances

  • Hemoglobins
  • Proto-Oncogene Proteins
  • Thalidomide
  • Protein-Tyrosine Kinases
  • JAK2 protein, human
  • Janus Kinase 2
  • Lenalidomide