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Blood, 19 March 2009, Vol. 113, No. 12, pp. 2637-2645.
Prepublished online as a Blood First Edition Paper on November 3, 2008; DOI 10.1182/blood-2008-07-168583.


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CLINICAL TRIALS AND OBSERVATIONS

Clinical response and pharmacokinetics from a phase 1 study of an active dosing schedule of flavopiridol in relapsed chronic lymphocytic leukemia

Mitch A. Phelps*,1, Thomas S. Lin*,2, Amy J. Johnson2, Eunju Hurh3, Darlene M. Rozewski3, Katherine L. Farley1, Di Wu3, Kristie A. Blum2, Beth Fischer2, Sarah M. Mitchell2, Mollie E. Moran2, Michelle Brooker-McEldowney2, Nyla A. Heerema4, David Jarjoura5, Larry J. Schaaf1,3, John C. Byrd2,6, Michael R. Grever2, and James T. Dalton3

1 Comprehensive Cancer Center, 2 Division of Hematology-Oncology, Department of Internal Medicine, 3 Division of Pharmaceutics, College of Pharmacy, 4 Department of Pathology, College of Medicine, 5 Division of Biostatistics, College of Public Health, and 6 Division of Medicinal Chemistry, College of Pharmacy, The Ohio State University, Columbus

We previously reported interim results of a phase 1 trial in patients with chronic lymphocytic leukemia (CLL) whereby flavopiridol was administered intravenously as a 30-minute bolus followed by 4-hour infusion. We now report full pharmacokinetic (PK) data, correlations of PK with clinical outcomes, and final response and progression-free survival (PFS). Twenty-one (40%) of 52 patients with relapsed CLL achieved a partial response (PR) with a median PFS of 12 months. Responders included 17 (40%) of 43 fludarabine refractory patients, 7 (39%) of 18 patients with del(17p13), and 14 (74%) of 19 patients with del(11q22). Six responders received repeat therapy at relapse, and 5 responded again with a second median PFS of 10 months. Noncompartmental analysis and nonlinear mixed effects modeling was used to estimate PK parameters and evaluate covariates. Two-compartment population parameter estimates were 31.4 L/h, 65.8 L, 8.49 L/h, and 157 L for CL, V1, Q, and V2, respectively. Flavopiridol area under the plasma concentration-time curve (AUC) correlated with clinical response and cytokine release syndrome, and glucuronide metabolite AUC correlated with tumor lysis syndrome. These composite results confirm high activity of this pharmacokinetically derived schedule in relapsed, genetically high-risk CLL. Furthermore, PK describes some, but not all, variability in response and toxicity.


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