pubmed-article:1381626 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:1381626 | lifeskim:mentions | umls-concept:C0079459 | lld:lifeskim |
pubmed-article:1381626 | lifeskim:mentions | umls-concept:C0024305 | lld:lifeskim |
pubmed-article:1381626 | lifeskim:mentions | umls-concept:C0027947 | lld:lifeskim |
pubmed-article:1381626 | lifeskim:mentions | umls-concept:C0282440 | lld:lifeskim |
pubmed-article:1381626 | lifeskim:mentions | umls-concept:C1096777 | lld:lifeskim |
pubmed-article:1381626 | lifeskim:mentions | umls-concept:C1512043 | lld:lifeskim |
pubmed-article:1381626 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:1381626 | pubmed:dateCreated | 1992-10-13 | lld:pubmed |
pubmed-article:1381626 | pubmed:abstractText | The effect of granulocyte colony-stimulating factor (G-CSF) on neutropenia, infection, and cytotoxic chemotherapy administration was studied in a randomized trial in patients receiving intensive weekly chemotherapy for non-Hodgkin's lymphoma (NHL). Eighty patients (aged 16 to 71 years) with high-grade NHL (Kiel) of any stage were randomized to receive VAPEC-B chemotherapy alone (39 patients) or with G-CSF administered as a daily subcutaneous dose of 230 micrograms/m2 (41 patients). Prophylactic ketoconazole and cotrimoxazole were administered to all patients throughout treatment. The protocol specified identical dose modification and antibiotic treatment criteria bor both groups. Neutropenia (absolute neutrophil count [ANC] less than 1.0 x 10(9)/L) occurred in 15 of 41 (37%) of the G-CSF-treated patients and in 33 of 39 (85%) of the controls, giving a relative risk for control patients of 2.31 (95% confidence interval [CI], [1.51, 3.54]; P = .00001). Fever (greater than or equal to 37.5 degrees C) with neutropenia (ANC less than 1.0 x 10(9)/L) occurred in 9 of 41 (22%) of the G-CSF group and in 17 of 39 (44%) of the controls (relative risk for control, 2.26; 95% CI [1.01, 5.06]; P = .04). There were fewer treatment delays, with shorter duration (P = .01) in patients receiving G-CSF. Chemotherapy doses were reduced in 4 of 41 (10%) of the G-CSF patients and 13 of 39 (33%) of the controls (P = .01). The dose intensity of cytotoxic chemotherapy was significantly increased in patients receiving G-CSF (median of 95% in G-CSF group compared with 83% in control patients). Three vascular deaths occurred in the G-CSF group. Delays in the control group most commonly resulted from neutropenia (19 patients, compared with 2 patients in the G-CSF-treated group, P = .000007). Severe mucositis was the major dose-limiting toxicity in G-CSF-treated patients, but did not occur more frequently than in controls (15 patients in each group). Overall, patients randomized to receive G-CSF achieved a greater dose intensity than control patients, but this did not result in significant differences in drug toxicity (other than neutropenia), intravenous antibiotic usage, or hospitalization between the two groups. | lld:pubmed |
pubmed-article:1381626 | pubmed:language | eng | lld:pubmed |
pubmed-article:1381626 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1381626 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:1381626 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:1381626 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:1381626 | pubmed:month | Sep | lld:pubmed |
pubmed-article:1381626 | pubmed:issn | 0006-4971 | lld:pubmed |
pubmed-article:1381626 | pubmed:author | pubmed-author:BentleyJJ | lld:pubmed |
pubmed-article:1381626 | pubmed:author | pubmed-author:CrowtherDD | lld:pubmed |
pubmed-article:1381626 | pubmed:author | pubmed-author:WilkinsonP... | lld:pubmed |
pubmed-article:1381626 | pubmed:author | pubmed-author:JamesRR | lld:pubmed |
pubmed-article:1381626 | pubmed:author | pubmed-author:KaneKK | lld:pubmed |
pubmed-article:1381626 | pubmed:author | pubmed-author:DeakinD PDP | lld:pubmed |
pubmed-article:1381626 | pubmed:author | pubmed-author:GurnerAA | lld:pubmed |
pubmed-article:1381626 | pubmed:author | pubmed-author:RadfordJ AJA | lld:pubmed |
pubmed-article:1381626 | pubmed:author | pubmed-author:PettengellRR | lld:pubmed |
pubmed-article:1381626 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:1381626 | pubmed:day | 15 | lld:pubmed |
pubmed-article:1381626 | pubmed:volume | 80 | lld:pubmed |
pubmed-article:1381626 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:1381626 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:1381626 | pubmed:pagination | 1430-6 | lld:pubmed |
pubmed-article:1381626 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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pubmed-article:1381626 | pubmed:year | 1992 | lld:pubmed |
pubmed-article:1381626 | pubmed:articleTitle | Granulocyte colony-stimulating factor to prevent dose-limiting neutropenia in non-Hodgkin's lymphoma: a randomized controlled trial. | lld:pubmed |
pubmed-article:1381626 | pubmed:affiliation | Cancer Research Campaign Department of Medical Oncology, Christie Hospital NHS Trust, Manchester, UK. | lld:pubmed |
pubmed-article:1381626 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:1381626 | pubmed:publicationType | Clinical Trial | lld:pubmed |
pubmed-article:1381626 | pubmed:publicationType | Randomized Controlled Trial | lld:pubmed |
pubmed-article:1381626 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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