pubmed-article:12424538 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:12424538 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:12424538 | lifeskim:mentions | umls-concept:C0001675 | lld:lifeskim |
pubmed-article:12424538 | lifeskim:mentions | umls-concept:C0087111 | lld:lifeskim |
pubmed-article:12424538 | lifeskim:mentions | umls-concept:C0008976 | lld:lifeskim |
pubmed-article:12424538 | lifeskim:mentions | umls-concept:C0001554 | lld:lifeskim |
pubmed-article:12424538 | lifeskim:mentions | umls-concept:C0034656 | lld:lifeskim |
pubmed-article:12424538 | lifeskim:mentions | umls-concept:C0079459 | lld:lifeskim |
pubmed-article:12424538 | lifeskim:mentions | umls-concept:C0023449 | lld:lifeskim |
pubmed-article:12424538 | lifeskim:mentions | umls-concept:C0010711 | lld:lifeskim |
pubmed-article:12424538 | lifeskim:mentions | umls-concept:C0220825 | lld:lifeskim |
pubmed-article:12424538 | lifeskim:mentions | umls-concept:C0023981 | lld:lifeskim |
pubmed-article:12424538 | lifeskim:mentions | umls-concept:C0086960 | lld:lifeskim |
pubmed-article:12424538 | lifeskim:mentions | umls-concept:C0205421 | lld:lifeskim |
pubmed-article:12424538 | lifeskim:mentions | umls-concept:C1554217 | lld:lifeskim |
pubmed-article:12424538 | pubmed:issue | 10 | lld:pubmed |
pubmed-article:12424538 | pubmed:dateCreated | 2002-11-8 | lld:pubmed |
pubmed-article:12424538 | pubmed:abstractText | In acute lymphoblastic leukemia (ALL), treatment with granulocyte colony stimulating factor (G-CSF) during remission induction shortens granulocytopenia and may decrease morbidity due to infections. However, the optimal timing of G-CSF administration after chemotherapy is not known. In a prospective randomized multi-center study, adult ALL patients were treated with high-dose ARA-C [HDAC, 3 g/m(2) bid (1 g/m(2) bid for T-ALL) days 1-4] and mitoxantrone (MI 10 mg/m(2) days 3-5). They were randomized to receive recombinant human G-CSF (Lenograstim) 263 micro g/day SC starting either from day 12 (Group 1) or day 17 (Group 2). Fifty-five patients (41 male, 14 female) with a median age of 34 years (range: 18-55 years) were enrolled into the study; 50 patients were evaluable. The median duration of neutropenia <500/ micro l after HDAC/MI was 12 days (range: 7-22 days) in the early G-CSF Group 1 and also 12 days (range: 4-22 days) in the late G-CSF Group 2; this was shorter than in the historical control group (15 days, range: 4-43 days, n=46) where the patients received identical cytotoxic treatment without G-CSF. Seventeen infections were observed in 14 patients in Group 1 (47%) and 13 infections in 10 patients in Group 2 (50%) compared to 27 infections in 49 patients of the historical control (54%). In Group 1, the patients received a median of 11 injections with G-CSF (range: 7-22) compared to 7 injections (range: 4-19) in Group 2. The total administered dose of G-CSF in Group 2 was significantly reduced by 40% ( P<0.0001). The delayed start of G-CSF after HDAC/MI in ALL achieves the same clinical benefit compared to the earlier initiation of G-CSF. The reduction of treatment costs by reducing the total G-CSF dose may be important in future treatment with this hematopoietic growth factor. | lld:pubmed |
pubmed-article:12424538 | pubmed:language | eng | lld:pubmed |
pubmed-article:12424538 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12424538 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:12424538 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12424538 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12424538 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:12424538 | pubmed:month | Oct | lld:pubmed |
pubmed-article:12424538 | pubmed:issn | 0939-5555 | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:HoelzerDD | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:HartmannFF | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:SchottDD | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:RascheHH | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:FiedlerFF | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:HuberCC | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:FrankeAA | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:RudolphCC | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:BergmannLL | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:GanserAA | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:BalleisenLL | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:IlligerH JHJ | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:PasoldRR | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:OttmannO GOG | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:SeipeltGG | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:PottCC | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:ReutzelRR | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:HofmannW KWK | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:GökbugetNN | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:SchoeffskiOO | lld:pubmed |
pubmed-article:12424538 | pubmed:author | pubmed-author:LangenhanSS | lld:pubmed |
pubmed-article:12424538 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:12424538 | pubmed:volume | 81 | lld:pubmed |
pubmed-article:12424538 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:12424538 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:12424538 | pubmed:pagination | 570-4 | lld:pubmed |
pubmed-article:12424538 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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pubmed-article:12424538 | pubmed:year | 2002 | lld:pubmed |
pubmed-article:12424538 | pubmed:articleTitle | Prospective randomized trial to evaluate two delayed granulocyte colony stimulating factor administration schedules after high-dose cytarabine therapy in adult patients with acute lymphoblastic leukemia. | lld:pubmed |
pubmed-article:12424538 | pubmed:affiliation | Department of Hematology and Oncology, Johann Wolfgang Goethe University Hospital, Theodor-Stern-Kai 7, 60596 Frankfurt/Main, Germany. W.K.Hofmann@em.uni-frankfurt.de | lld:pubmed |
pubmed-article:12424538 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:12424538 | pubmed:publicationType | Clinical Trial | lld:pubmed |
pubmed-article:12424538 | pubmed:publicationType | Randomized Controlled Trial | lld:pubmed |
pubmed-article:12424538 | pubmed:publicationType | Multicenter Study | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:12424538 | lld:pubmed |