Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10908779 | Leukemia Research | 2013 | 5 Pages |
Abstract
Alvocidib has demonstrated efficacy in high-risk chronic lymphocytic leukemia (CLL) patients. In this phase I study, we combined cyclophosphamide, alvocidib and rituximab (CAR) in a schema designed to mitigate tumor lysis syndrome (TLS) seen previously with alvocidib. Nine nucleoside analog-naïve, high-risk patients received escalating doses of CAR therapy. Dose limiting toxicity was not experienced. No instances of TLS were observed. Patient responses included three complete remissions and four partial remissions. CAR was tolerable and active in high-risk CLL patients without TLS toxicity. With continued monitoring of toxicities, a phase Ib/II study of this combination as frontline therapy is warranted.
Keywords
b2mCLLdel(17p)DLTMTDIgVHECoGCRSWBCTLSORRNCICDKPFsbeta 2 microglobulinprogression-free survivaloverall survivalprogressive diseaseMaximum tolerated dosedose limiting toxicityCytokine Release SyndromeTumor lysis syndromeeastern cooperative oncology groupChemoimmunotherapypharmacokineticFlavopiridolChronic lymphocytic leukemiaCARimmunoglobulin heavy chain variable regioncyclin-dependent kinase inhibitorNational Cancer Instituteoverall response ratecomplete responsecyclin-dependent kinasewhite blood cell
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Authors
Deborah M. Stephens, Amy S. Ruppert, Kami Maddocks, Leslie Andritsos, Robert Baiocchi, Jeffrey Jones, Amy J. Johnson, Lisa L. Smith, Yuan Zhao, Yonghua Ling, Junan Li, Mitch A. Phelps, Michael R. Grever, John C. Byrd, Joseph M. Flynn,