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| Title: | Timely withdrawal of G-CSF reduces the occurrence of thrombocytopenia during dose-dense chemotherapy. |
| Author(s): | Timmer-Bonte, A. (306041189) Mulder, P.H.M. de (069323402) Peer, P.G.M. (073002763) Beex, L.V.A.M. (068435223) Tjan-Heijnen, V.C. (298975777) |
| Publication year: | 2005 |
| Document type: | Article / Letter to editor |
| Journal: | Breast Cancer Research and Treatment |
| ISSN: | 0167-6806 |
| Volume: | vol. 93 |
| Issue: | iss. 2 |
| Start page: | p. 117 |
| End page: | p. 123 |
| Abstract: | BACKGROUND: Post chemotherapy Granulocyte colony stimulating factor (G-CSF) reduces leucopenia, while G-CSF priming shortly before chemotherapy increases myelotoxicity. We performed a trial with a two-schedule crossover design to determine the optimal G-CSF schedule for densified 2-weekly chemotherapy. METHODS: During 2-weekly chemotherapy days 1 and 2, G-CSF was given on days 3-10, with a G-CSF-free interval before the next chemotherapy cycle of 5 days, or on days 3-13, with a G-CSF-free interval of 2 days. In schedule A, cycle II was preceded by a 5 days, cycle III and IV by a 2 days and cycle V by a 5 days G-CSF free interval. In schedule B, this was 2, 5, 5, and 2 days, respectively. RESULTS: Intra-patient comparison for cycles II versus III and cycles IV versus V showed that platelet (PLT) nadir count was significantly lower for cycles preceded by a 2-days compared to a 5-days G-CSF free interval: mean difference 45.7 x 10(9)/l (95% CI 33.2-58.2, p = 0.0001). Neutrophil count did not differ significantly (p = 0.85). CONCLUSION: Timely withdrawal of G-CSF in dose-dense chemotherapy reduces chemotherapy-related thrombocytopenia. Leucopenia was not aggravated, reflecting a protective effect of post-chemotherapy G-CSF. |
| Subject: | EBP 2: Effective Hospital Care UMCN 1.5: Interventional oncology |
| Organization: | Medical Oncology Epidemiology, Biostatistics & HTA |
| Appears in Collections: | Academic bibliography
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Please use this identifier to cite or link to this item:
http://hdl.handle.net/2066/48504
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