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Phase II study of three dose levels of continuous erythropoietin receptor activator (C.E.R.A.) in anaemic patients with aggressive non-Hodgkin's lymphoma receiving combination chemotherapy.

AbstractAnaemia is a common complication in the treatment of patients with aggressive non-Hodgkin lymphoma (NHL), but there are no published data on the effect of erythropoiesis-stimulating agents in such patients. This is the first open-label, phase II, dose-finding study to evaluate the efficacy and safety of continuous erythropoietin receptor activator (C.E.R.A.). Ninety-three anaemic patients with aggressive NHL who were receiving chemotherapy (including many advanced NHL, heavily pretreated patients) were randomised to receive 2.1, 4.2 or 6.3 microg/kg C.E.R.A. subcutaneously once every 3 weeks for 12 weeks. Haematopoietic response was achieved in 45%, 57% and 65% of patients at the respective dose level. During weeks 5-13, the mean haemoglobin changes from baseline in the intent-to-treat population were increases of 0.2, 2.4, and 5.7 g/l in the 2.1, 4.2, and 6.3 microg/kg treatment groups, respectively, and 4.4, 5.7 and 6.8 g/l in the per-protocol population at the respective dose levels. C.E.R.A. was generally well tolerated in all three groups. C.E.R.A. appeared to have dose-dependent clinical activity in most anaemic patients with aggressive NHL who were receiving chemotherapy.
AuthorsAnders Osterborg, Juan Luis Steegmann, Andrzej Hellmann, Stephen Couban, Jiri Mayer, Joseph E Eid (Affiliation: Departments of Oncology and Haematology, Karolinska University Hospital, Stockholm, Sweden. anders.osterborg at karolinska.se)
JournalBritish journal of haematology (Br J Haematol) Vol. 136 Issue 5 Pg. 736-44 (Mar 2007) ISSN: 0007-1048 [Print] England
PMID17313376 (Publication Type: Clinical Trial, Phase II, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
Chemical References
  • Polyethylene Glycols
  • continuous erythropoietin receptor activator
  • Erythropoietin
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Anemia (chemically induced, drug therapy)
  • Antineoplastic Combined Chemotherapy Protocols (adverse effects)
  • Dose-Response Relationship, Drug
  • Erythropoietin (administration & dosage, adverse effects, therapeutic use)
  • Female
  • Humans
  • Lymphoma, B-Cell (drug therapy)
  • Male
  • Middle Aged
  • Polyethylene Glycols (administration & dosage, adverse effects, therapeutic use)
  • Treatment Outcome

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