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Ifosfamide in Sarcomas: Is It a Schedule-Dependent Drug?

Patel, Shreyaskumar R.; Benjamin, Robert S.
Cancer Investigation , Volume 14 (3) Informa HealthcareJan 1, 1996

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Ifosfamide in Sarcomas: Is It a Schedule-Dependent Drug?

Abstract

Cancer Investigation, 14(3), 290-291 (1996) Ifosfamide in Sarcomas: Is It a Schedule-Dependent Drug? Shreyaskumar R. Patel, M.D., and Robert S. Benjamin, M.D. Depaflment of MelanomdSarcomaMedical Oncology Tbe Universityof TexasM.D. Anderson Cancer Center 1 1 Holcombe Boulevard 5 5 Houston, Texas 77030 The availability of Mesna in the early 1980s allowed the resurgence of interest in ifosfamide. Several clinical trials conducted through the early to late 1980s in patients with doxorubicin-refractory sarcomas established the activity of ifosfamide in sarcomas with response rates varying from 15 to 25%, when administered at “standard doses” of up to 10 g/m2 with Mesna. Ifosfamide is an alkylating agent with cell cycle specificity but phase nonspecificity, and therefore, it would be expected to have a linear dose-response relationship. Data from sequential studies performed at The University of Texas M. D. Anderson Cancer Center do indeed support the dose-response relationship (1). Several trials evaluating “high-dose ifosfamide,” which in general refers to doses greater than 12 g/m2/cycle,have been reported in the last 5 years (2-6). Our initial attempt at evaluating high-dose ifosfarnide (14 g/m2/cycle)began in 1990. Due to obvious concerns of renal and neurotoxicity, we chose to adopt a continuous infusion schedule (4 g/m2/24hr x 3),
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/lp/informa-healthcare/ifosfamide-in-sarcomas-is-it-a-schedule-dependent-drug-tnJ6bzKHwv
Title
Ifosfamide in Sarcomas: Is It a Schedule-Dependent Drug?
Author(s)
Patel, Shreyaskumar R.; Benjamin, Robert S.
Journal
Cancer Investigation , Volume 14 (3) Informa Healthcare – Jan 1, 1996
Publisher
Informa UK Ltd
Copyright
© 1996 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted
Subject
Editorial Article
ISSN
0735-7907
eISSN
1532-4192
D.O.I.
10.3109/07357909609012153
Publisher site
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