Literature DB >> 28421558

Recombinant Granulocyte-Macrophage Colony-Stimulating Factor (rGM-CSF) : A Review of its Pharmacological Properties and Prospective Role in the Management of Myelosuppression.

Susan M Grant1, Rennie C Heel1.   

Abstract

Recombinant granulocyte-macrophage colony-stimulating factor (rGM-CSF) is a polypeptide hormone produced through recombinant DNA technologies in glycosylated (yeast or mammalian expression systems) or nonglycosylated (Escherichia coli expression system) form. It is a multilineage haematopoietin which stimulates proliferation and differentiation of bone marrow myeloid progenitors and increases peripheral white blood cell counts when administered systemically. Treatment is generally well tolerated, although mild to moderate flu-like symptoms are common and rGM-CSF-induced fever and fluid retention may be problematic in occasional patients. rGM-CSF accelerates recovery of peripheral neutrophil counts after bone marrow transplantation, and results of a placebo-controlled randomised trial correlate this with reduced infectious episodes and shortened length of hospitalisation in patients with lymphoid malignancies. A substantial number of patients with graft failure after bone marrow transplantation also respond to rGM-CSF. The duration of myelosuppression secondary to cancer chemotherapy can be significantly reduced by rGM-CSF which has permitted investigation of antineoplastic dose-intensity escalation. In some haematopoietic disorders (e.g. aplastic anaemia, myelodysplasia and neutropenia secondary to HIV infection and antiviral therapy), rGM-CSF produces clinically useful increases in peripheral blood granulocyte counts, although the effect is generally not sustained after drug withdrawal. The potential for rGM-CSF to stimulate proliferation of the abnormal clone in myelodysplasia and in acute myelogenous leukaemia following induction therapy is of concern. Available data suggest, however, that with appropriate monitoring and exclusion of high-risk patients this serious potential risk can be avoided, and that myelopoiesis is enhanced in such patients by rGM-CSF treatment. Recombinant colony-stimulating factors are a new therapeutic modality; hence many aspects of their use remain to be clarified. Nonetheless, as one of a small group of novel agents rGM-CSF has major potential in the management of myelosuppression secondary to cytoreductive therapy with or without bone marrow transplantation, and in amelioration of disturbed myelopoiesis. It represents an important application of biotechnology to a difficult area of therapeutics.

Entities:  

Year:  1992        PMID: 28421558     DOI: 10.2165/00003495-199243040-00008

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


  325 in total

1.  Treatment of neutropenia associated with dyskeratosis congenita with granulocyte-macrophage colony-stimulating factor.

Authors:  C L Russo; B E Glader; R J Israel; F Galasso
Journal:  Lancet       Date:  1990-09-22       Impact factor: 79.321

2.  The effects of recombinant human granulocyte-macrophage colony-stimulating factor on phagocyte kinetics in man.

Authors:  D C Linch; S Devereux; I E Addison
Journal:  Behring Inst Mitt       Date:  1988-08

3.  Acceleration of autologous hematopoietic recovery by GM-CSF after allograft rejection.

Authors:  G Bandini; G Rosti; M Cavo; L Albertazzi; S Tura
Journal:  Haematologica       Date:  1989 Nov-Dec       Impact factor: 9.941

4.  Cell-dose effect in circulating stem-cell autografting.

Authors:  L B To; P G Dyson; C A Juttner
Journal:  Lancet       Date:  1986-08-16       Impact factor: 79.321

5.  Binding of G-CSF, GM-CSF, tumor necrosis factor-alpha, and gamma-interferon to cell surface receptors on human myeloid leukemia cells triggers rapid tyrosine and serine phosphorylation of a 75-Kd protein.

Authors:  J P Evans; A R Mire-Sluis; A V Hoffbrand; R G Wickremasinghe
Journal:  Blood       Date:  1990-01-01       Impact factor: 22.113

6.  Pharmacokinetics of human granulocyte-macrophage colony-stimulating factor using a sensitive immunoassay.

Authors:  J Cebon; P Dempsey; R Fox; G Kannourakis; E Bonnem; A W Burgess; G Morstyn
Journal:  Blood       Date:  1988-10       Impact factor: 22.113

7.  Recombinant human GM-CSF following chemotherapy in high-risk AML.

Authors:  T Buechner; W Hiddemann; M Koenigsmann; M Zuehlsdorf; B Woermann; A Boeckmann; E Aguion Freire; G Innig; G Maschmeyer; W D Ludwig
Journal:  Bone Marrow Transplant       Date:  1990-07       Impact factor: 5.483

8.  Stimulation of granulopoiesis in patients with malignancy by recombinant human granulocyte-macrophage colony-stimulating factor: assessment of two routes of administration.

Authors:  F Herrmann; A Ganser; A Lindemann; G Schulz; M Lübbert; D Hoelzer; R Mertelsmann
Journal:  J Biol Response Mod       Date:  1990-10

9.  Effect of granulocyte-macrophage colony-stimulating factor on neutropenia and related morbidity induced by myelotoxic chemotherapy.

Authors:  F Herrmann; G Schulz; M Wieser; K Kolbe; U Nicolay; M Noack; A Lindemann; R Mertelsmann
Journal:  Am J Med       Date:  1990-06       Impact factor: 4.965

10.  Granulocyte-macrophage colony-stimulating factor enhances the cytotoxic effects of cytosine arabinoside in acute myeloblastic leukemia and in the myeloid blast crisis phase of chronic myeloid leukemia.

Authors:  S A Cannistra; P Groshek; J D Griffin
Journal:  Leukemia       Date:  1989-05       Impact factor: 11.528

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  4 in total

Review 1.  Clinical toxicity of cytokines used as haemopoietic growth factors.

Authors:  T Vial; J Descotes
Journal:  Drug Saf       Date:  1995-12       Impact factor: 5.606

Review 2.  Recombinant granulocyte-macrophage colony-stimulating factor (rGM-CSF): an appraisal of its pharmacoeconomic status in neutropenia associated with chemotherapy and autologous bone marrow transplant.

Authors:  K L Goa; H M Bryson
Journal:  Pharmacoeconomics       Date:  1994-01       Impact factor: 4.981

3.  Recombinant granulocyte colony-stimulating factor (rG-CSF): pharmacoeconomic considerations in chemotherapy-induced neutropenia.

Authors:  D Faulds; N J Lewis; R J Milne
Journal:  Pharmacoeconomics       Date:  1992-04       Impact factor: 4.981

Review 4.  Cytokine signaling convergence regulates the microglial state transition in Alzheimer's disease.

Authors:  Shun-Fat Lau; Amy K Y Fu; Nancy Y Ip
Journal:  Cell Mol Life Sci       Date:  2021-04-13       Impact factor: 9.261

  4 in total

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