Selecting Drug Combinations Based on Total Equivalent Dose (Dose Intensity)
- 19 September 1990
- journal article
- research article
- Published by Oxford University Press (OUP) in JNCI Journal of the National Cancer Institute
- Vol. 82 (18) , 1469-1476
- https://doi.org/10.1093/jnci/82.18.1469
Abstract
We describe a mathematical model for selecting cytotoxic drugs and dosages for a combination regimen based on the antitumor activities of the drugs given as single agents and their organ-specific maximum tolerated doses. The regimen defined maximizes an approximate measure of antitumor effect subject to constraints on combined toxicity. This approach does not assume that the underlying dose—response curve is steep; nor does it assume that maximally dose-intense regimens are clinically appropriate in all situations. Whether the identified regimen is superior to standard treatments should be determined by prospective, randomized clinical trials. Determining which drugs to combine and in what proportions to combine them offers combinatorially huge numbers of possibilities. The method described here offers one approach to identifying combinations worthy of evaluation in prospective trials. [J Natl Cancer Inst 82:1469–1476, 1990]This publication has 6 references indexed in Scilit:
- A Comparison of the Toxicity and Efficacy of Cisplatin and Carboplatin in Advanced Ovarian CancerActa Oncologica, 1989
- Dose intensity analysis of chemotherapy regimens in ovarian carcinoma.Journal of Clinical Oncology, 1987
- Analysis of dose intensity for adjuvant chemotherapy trials in stage II breast cancer.Journal of Clinical Oncology, 1986
- High-Dose Cisplatin in Hypertonic SalineAnnals of Internal Medicine, 1984
- IMPROVED METHOD FOR ANALYZING SURVIVAL DATA FROM COMBINATION CHEMOTHERAPY EXPERIMENTS1979
- A Unified Theory for Quantal Responses to Mixtures of Drugs: Competitive ActionPublished by JSTOR ,1964