Lenograstim: an update of its pharmacological properties and use in chemotherapy-induced neutropenia and related clinical settings.

作者: Christopher J. Dunn , Karen L. Goa

DOI: 10.2165/00003495-200059030-00017

关键词:

摘要: UNLABELLED Lenograstim is the glycosylated recombinant form of human granulocyte colony stimulating factor. The drug used to reduce risk life-threatening infection in patients with neutropenia, particularly after cytotoxic chemotherapy. accelerates neutrophil recovery significantly chemotherapy, beneficial effects on clinical end-points such as incidence laboratory-confirmed and length hospital stay. Chemotherapy dose intensity has also been increased receiving lenograstim, notably those breast or small cell lung cancer, although improvements tumour response survival have not demonstrated. assists undergoing bone marrow transplantation, stimulates production peripheral blood stem cells (PBSCs) for autologous transfusion aggressive mobilises CD34+ more efficiently unit terms than filgrastim successfully mobilise PBSCs from healthy donors allogeneic transplantation. Randomised trials shown increases rates disease remission lenograstim therapy acute myeloid leukaemia, no evidence stimulation malignant blasts. potential mobilisation nonmalignant autotransplantation chronic leukaemia. Other studies show efficacy lymphoblastic aplastic anaemia, children severe neutropenia reversal related antiviral AIDS, data are extensive. Cost analyses carried out a perspective, results inconclusive. Cost-effectiveness cost-benefit lacking at present. well tolerated, pain injection site reactions being reported most frequently trials. CONCLUSIONS confirmed valuable adjunct minimise haematological toxicity myelosuppressive chemotherapy disease. enhances rescue, PBSC mobilisation. Data indicate benefit disorders, blast proliferation. Further required assess fully pharmacoeconomic implications use other growth factors, provide management disease-related clarify its position relative filgrastim.

参考文章(112)
Karen L. Goa, Harriet M. Bryson, Recombinant Granulocyte-Macrophage Colony-Stimulating Factor (rGM-CSF) PharmacoEconomics. ,vol. 5, pp. 56- 77 ,(1994) , 10.2165/00019053-199405010-00008
Bruce M. Camitta, Rainer Storb, E. Donnall Thomas, Aplastic anemia (first of two parts): pathogenesis, diagnosis, treatment, and prognosis. The New England Journal of Medicine. ,vol. 306, pp. 645- 652 ,(1982) , 10.1056/NEJM198203183061105
D. Przepiorka, R. Champlin, P. Anderlini, M. Körbling, Blood stem cell procurement: Donor safety issues Bone Marrow Transplantation. ,vol. 21, ,(1998)
A Bacigalupo, G Broccia, G Corda, W Arcese, M Carotenuto, A Gallamini, F Locatelli, PG Mori, P Saracco, G Todeschini, Antilymphocyte globulin, cyclosporin, and granulocyte colony- stimulating factor in patients with acquired severe aplastic anemia (SAA): a pilot study of the EBMT SAA Working Party Blood. ,vol. 85, pp. 1348- 1353 ,(1995) , 10.1182/BLOOD.V85.5.1348.BLOODJOURNAL8551348
NS Young, AJ Barrett, The Treatment of Severe Acquired Aplastic Anemia Blood. ,vol. 85, pp. 3367- 3377 ,(1995) , 10.1182/BLOOD.V85.12.3367.BLOODJOURNAL85123367
Diana Faulds, Nancy J.W. Lewis, Richard J. Milne, Recombinant Granulocyte Colony-Stimulating Factor (rG-CSF) PharmacoEconomics. ,vol. 1, pp. 231- 249 ,(1992) , 10.2165/00019053-199201040-00002
M Oh-eda, M Hasegawa, K Hattori, H Kuboniwa, T Kojima, T Orita, K Tomonou, T Yamazaki, N Ochi, O-linked sugar chain of human granulocyte colony-stimulating factor protects it against polymerization and denaturation allowing it to retain its biological activity. Journal of Biological Chemistry. ,vol. 265, pp. 11432- 11435 ,(1990) , 10.1016/S0021-9258(19)38416-9