Abstract | BACKGROUND: PATIENTS AND METHODS: All patients had colorectal adenocarcinoma with measurable disease and no prior chemotherapy for metastatic disease. Patients were randomized to receive either ISIS 3521 or ISIS 5132 at a dose of 2 mg/kg/day as a continuous i.v. infusion 21 of 28 days. Cycles were repeated as long as progression was not seen, and doses of both agents were modified according to toxic effects. A two-arm study design was used with each study arm considered independently. Steady-state blood levels of both antisense molecules were measured on days 8, 15, and 22 of the first cycle of therapy. RESULTS: Thirty-seven eligible patients were enrolled, and 32 were evaluable for response (17 receiving ISIS 3521 and 15 receiving ISIS 5132). No responses were noted. Four of the patients receiving ISIS 3521 had stable disease, and 5 patients receiving ISIS 5132 were stable. CONCLUSION: Neither ISIS 5132 nor ISIS 3521given in the dose and schedule studied induced objective responses in untreated colorectal cancer patients.
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Authors | M Christine Cripps, Alvaro T Figueredo, Amit M Oza, Marianne J Taylor, Anthony L Fields, John T Holmlund, Lynn W McIntosh, Richard S Geary, Elizabeth A Eisenhauer |
Journal | Clinical cancer research : an official journal of the American Association for Cancer Research
(Clin Cancer Res)
Vol. 8
Issue 7
Pg. 2188-92
(Jul 2002)
ISSN: 1078-0432 [Print] United States |
PMID | 12114419
(Publication Type: Clinical Trial, Clinical Trial, Phase II, Comparative Study, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- Enzyme Inhibitors
- Isoenzymes
- Oligodeoxyribonucleotides, Antisense
- Thionucleotides
- ISIS 3521
- ISIS 5132
- Proto-Oncogene Proteins c-raf
- PRKCA protein, human
- Protein Kinase C
- Protein Kinase C-alpha
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Topics |
- Adenocarcinoma
(drug therapy, genetics, secondary)
- Adult
- Aged
- Antineoplastic Agents
(adverse effects, therapeutic use)
- Colorectal Neoplasms
(drug therapy, genetics, pathology)
- Dose-Response Relationship, Drug
- Enzyme Inhibitors
(adverse effects, therapeutic use)
- Female
- Humans
- Infusions, Intravenous
- Isoenzymes
(antagonists & inhibitors, genetics)
- Male
- Maximum Tolerated Dose
- Middle Aged
- Oligodeoxyribonucleotides, Antisense
(adverse effects, therapeutic use)
- Protein Kinase C
(antagonists & inhibitors, genetics)
- Protein Kinase C-alpha
- Proto-Oncogene Proteins c-raf
(antagonists & inhibitors, genetics)
- Thionucleotides
(adverse effects, therapeutic use)
- Treatment Outcome
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