Literature DB >> 8808169

Epoetin beta. A review of its pharmacological properties and clinical use in the management of anaemia associated with chronic renal failure.

C J Dunn1, A Markham.   

Abstract

Epoetin beta is a recombinant form of erythropoietin, the hormone responsible for the maintenance of erythropoiesis. The drug binds to and activates receptors on erythroid progenitor cells which then develop into mature erythrocytes. Epoetin beta increases reticulocyte counts, haemoglobin levels and haematocrit in a dose-proportional manner. These changes are accompanied by beneficial cardiovascular effects, including decreased cardiac output, resting heart rate and left ventricular hypertrophy in patients with chronic renal failure (CRF). Increases of 15 to 54% in haemoglobin levels and 17 to 60% in haematocrit were reported after subcutaneous or intravenous epoetin beta therapy in studies of 8 weeks' to 12 months' duration. Two multicentre clinical trials demonstrated clearly the superior efficacy of epoetin beta over placebo in 229 patients with CRF undergoing haemodialysis. Reduction or elimination of transfusion requirements was reported in studies where this parameter was measured. Comparative data indicate that dosage reductions of approximately 30% compared with intravenous therapy are possible when subcutaneous administration of epoetin beta is used. Haematocrit increased more rapidly in 5 multicentre studies in patients who received epoetin beta subcutaneously than in those who received the same dosage intravenously. Correction of anaemia with epoetin beta is associated with significant improvements in quality of life in patients with CRF. Available data indicate greatest cost-effectiveness in patients who are severely incapacitated by anaemia before treatment. The cost of administration of the drug may also be reduced by the use of the subcutaneous route. Hypertension may occur in patients who receive epoetin beta but may be minimised by avoiding rapid increases in haematocrit (> 0.5%/week), and is managed in most cases with control of fluid status and antihypertensive medication. Although clotting of the vascular access has not been conclusively linked to epoetin beta, caution is recommended in patients undergoing haemodialysis. Increased heparinisation is recommended to prevent clotting in dialysis equipment. Epoetin beta is more effective and/or better tolerated than alternative treatments (e.g. androgenic steroids) for anaemia associated with CRF. It also causes significant improvements in quality of life, exercise capacity and overall well-being. Results of clinical studies indicate that subcutaneous administration is desirable where possible in the majority of patients. Thus, epoetin beta has become established as an effective treatment for anaemia associated with CRF.

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Year:  1996        PMID: 8808169     DOI: 10.2165/00003495-199651020-00008

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  78 in total

1.  Assessment of pain after subcutaneous injection of erythropoietin in patients receiving haemodialysis.

Authors:  L A Frenken; H J van Lier; P G Gerlag; M den Hartog; R A Koene
Journal:  BMJ       Date:  1991-08-03

Review 2.  Epoetin: a pharmacoeconomic review of its use in chronic renal failure and its effects on quality of life.

Authors:  R Whittington; L B Barradell; P Benfield
Journal:  Pharmacoeconomics       Date:  1993-01       Impact factor: 4.981

3.  Effect of long-term epoetin beta therapy on the quality of life of hemodialysis patients.

Authors:  O L Deniston; F A Luscombe; D P Buesching; R E Richner; B S Spinowitz
Journal:  ASAIO Trans       Date:  1990 Jul-Sep

4.  Epoetin enhances erythropoiesis in normal men undergoing repeated phlebotomies.

Authors:  P A Abraham; C E Halstenson; M M Macres; J A Opsahl; B H Rank; M H Schwenk; L C Lasky; A Cohen; K C Lasseter; D L Smith
Journal:  Clin Pharmacol Ther       Date:  1992-08       Impact factor: 6.875

5.  Modifications of erythropoiesis in myelodysplastic syndromes treated with recombinant erythropoietin as evaluated by soluble transferrin receptor, high fluorescence reticulocytes and hypochromic erythrocytes.

Authors:  P Musto; S Modoni; G Alicino; A Savino; A Longo; C Bodenizza; A Falcone; G D'Arena; P Scalzulli; G Perla
Journal:  Haematologica       Date:  1994 Nov-Dec       Impact factor: 9.941

6.  Comparative pharmacokinetics and pharmacodynamics of epoetin alfa and epoetin beta.

Authors:  C E Halstenson; M Macres; S A Katz; J R Schnieders; M Watanabe; J T Sobota; P A Abraham
Journal:  Clin Pharmacol Ther       Date:  1991-12       Impact factor: 6.875

7.  The use of epoetin beta in anemic predialysis patients with chronic renal failure.

Authors:  K M Koch; R A Koene; D Messinger; O Quarder; P Scigalla
Journal:  Clin Nephrol       Date:  1995-09       Impact factor: 0.975

8.  Effect of recombinant human erythropoietin treatment in uremic patients on oxygen affinity of hemoglobin.

Authors:  P Brunet; Y Berland; T Merzouk; D Vanuxem; M Badier; H Klinkmann; A Crevat
Journal:  Nephron       Date:  1994       Impact factor: 2.847

9.  Effect of erythropoietin therapy on diet and dialysis clearances in hemodialysis patients.

Authors:  C J Kaupke; N D Vaziri; J R Sampson; K Atkins
Journal:  Int J Artif Organs       Date:  1990-04       Impact factor: 1.595

10.  Impact of epoetin beta on dialyzer clearance and heparin requirements.

Authors:  B S Spinowitz; J Arslanian; C Charytan; R A Golden; J Rascoff; M Galler
Journal:  Am J Kidney Dis       Date:  1991-12       Impact factor: 8.860

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  3 in total

Review 1.  Darbepoetin alfa.

Authors:  T Ibbotson; K L Goa
Journal:  Drugs       Date:  2001       Impact factor: 9.546

Review 2.  The Safety of Erythropoiesis-Stimulating Agents for the Treatment of Anemia Resulting from Chronic Kidney Disease.

Authors:  Nicolas Roberto Robles
Journal:  Clin Drug Investig       Date:  2016-06       Impact factor: 2.859

Review 3.  Epoetin Beta: a review of its clinical use in the treatment of anaemia in patients with cancer.

Authors:  Susan M Cheer; Antona J Wagstaff
Journal:  Drugs       Date:  2004       Impact factor: 9.546

  3 in total

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