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CI-980 for the Treatment of Recurrent or Progressive Malignant Gliomas: National Central Nervous System Consortium Phase I-II Evaluation of CI-980 |
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| Authors: | Lara J. Kunschner Howard Fine Kenneth Hess Kurt Jaeckle Athanassios P. Kyritsis W. K. Alfred Yung |
| Affiliation: | a Department of Neuro-Oncology, M. D. Anderson Cancer Center, University of Texas, Houston, TX, U.S.A.b Department of Biomathematics, M. D. Anderson Cancer Center, University of Texas, Houston, TX, U.S.A.c Allegheny Neurological Associates, Pittsburgh, Pennsylvania, U.S.A.d Dana Farber Cancer Institute, Boston, Massachusetts, U.S.A.e National Cancer Institute, Bethesda, Maryland, U.S.A.f Mayo Clinic, Jacksonville, Florida, U.S.A.g Ioannina University, Ioannina, Greece |
| Abstract: | Objective: The purpose of this phase I/II trial was to determine the maximal tolerated dose of CI-980, and determine efficacy against malignant glioma. Background: The CI-980 is a synthetic mitosis inhibitor that acts via the colchicine binding site on tubulin. Broad in vitro activity has been seen in a variety of human and murine tumor models. Phase I studies have demonstrated schedule dependent toxicity of CI-980. Dose-limiting toxicity was neurologic when CI-980 was given as a 24-hr infusion and hematologic when given over 72 hr at higher doses. Methods: Twenty-four patients ages 29-65 entered this study. Six patients were treated on the phase I arm at three escalating dose levels ranging from 10.5 to 13.5 mg/m2, given over 72 hr. Eighteen patients were then treated at the highest tolerated dose, 13.5 mg/m2 per cycle. Treatment response was based on serial MRI imaging characteristics. Results: The phase II study was stopped at the end of the first stage due to poor treatment response. There were no partial or complete responses, (0/24) 95% CI=0-14%. Four patients (4/24) had a best treatment response of stable disease/no change. Median time to progression for all patients was 6.4 weeks (95% CI: 6-9 weeks). Dose-limiting toxicity was grade 3-4 granulocytopenia. Three episodes of neurotoxicity manifested by a moderate cerebellar dysfunction were seen. Conclusions: These results fail to demonstrate the significant activity of CI-980 against recurrent glioma. |
| Keywords: | CI-980 Chemotherapy Malignant gliomas |
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