2002
DOI: 10.1038/sj.bjc.6600542
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Phase I study of docetaxel plus ifosfamide in patients with advanced cancer

Abstract: The aim of this study was to determine the maximum tolerated dose of a fixed dose of docetaxel when combined with continuous infusion ifosfamide, with and without G-CSF support, in the treatment of advanced cancer, and to evaluate antitumour activity of this combination. Thirty-one patients with advanced malignancies were treated with docetaxel 75 mg/m 2 intravenously on days 1, and ifosfamide at increasing dose levels from 1500 mg/m 2 /day to 2750 mg/m 2 /day as a continuous infusion from day 1 -3, every 3 we… Show more

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Cited by 3 publications
(2 citation statements)
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“…In 48 patients a response rate of 38% was observed, with a median survival of 8.5 months [24]. A phase I study of docetaxel 75 mg/m 2 day 1 and ifosfamide at increasing doses from 1,500 to 2,750 mg/m 2 as a continuous infusion, on days 1–3 every 3 weeks, was conducted in 31 patients; 3 complete responses and 3 partial responses were seen [26]. …”
Section: New Drug Combinationsmentioning
confidence: 99%
“…In 48 patients a response rate of 38% was observed, with a median survival of 8.5 months [24]. A phase I study of docetaxel 75 mg/m 2 day 1 and ifosfamide at increasing doses from 1,500 to 2,750 mg/m 2 as a continuous infusion, on days 1–3 every 3 weeks, was conducted in 31 patients; 3 complete responses and 3 partial responses were seen [26]. …”
Section: New Drug Combinationsmentioning
confidence: 99%
“…Three CRs and 3 PRs were seen. The recommended dose for future phase II studies is docetaxel 75 mg/m 2 on day 1 and IFO 2,500 mg/m 2 /day continuous infusion on days 1–3 [51]. …”
Section: Novel Combinations With Chemotherapeutic Agentsmentioning
confidence: 99%