Literature DB >> 19826119

Phase II study of flavopiridol in relapsed chronic lymphocytic leukemia demonstrating high response rates in genetically high-risk disease.

Thomas S Lin1, Amy S Ruppert, Amy J Johnson, Beth Fischer, Nyla A Heerema, Leslie A Andritsos, Kristie A Blum, Joseph M Flynn, Jeffrey A Jones, Weihong Hu, Mollie E Moran, Sarah M Mitchell, Lisa L Smith, Amy J Wagner, Chelsey A Raymond, Larry J Schaaf, Mitch A Phelps, Miguel A Villalona-Calero, Michael R Grever, John C Byrd.   

Abstract

PURPOSE: Patients with chronic lymphocytic leukemia (CLL) with high-risk genomic features achieve poor outcomes with traditional therapies. A phase I study of a pharmacokinetically derived schedule of flavopiridol suggested promising activity in CLL, irrespective of high-risk features. Given the relevance of these findings to treating genetically high-risk CLL, a prospective confirmatory study was initiated. PATIENTS AND METHODS: Patients with relapsed CLL were treated with single-agent flavopiridol, with subsequent addition of dexamethasone to suppress cytokine release syndrome (CRS). High-risk genomic features were prospectively assessed for response to therapy.
RESULTS: Sixty-four patients were enrolled. Median age was 60 years, median number of prior therapies was four, and all patients had received prior purine analog therapy. If patients tolerated treatment during week 1, dose escalation occurred during week 2. Dose escalation did not occur in four patients, as a result of severe tumor lysis syndrome; three of these patients required hemodialysis. Thirty-four patients (53%) achieved response, including 30 partial responses (PRs; 47%), three nodular PRs (5%), and one complete response (1.6%). A majority of high-risk patients responded; 12 (57%) of 21 patients with del(17p13.1) and 14 (50%) of 28 patients with del(11q22.3) responded irrespective of lymph node size. Median progression-free survival among responders was 10 to 12 months across all cytogenetic risk groups. Reducing the number of weekly treatments per cycle from four to three and adding prophylactic dexamethasone, which abrogated interleukin-6 release and CRS (P < or = .01), resulted in improved tolerability and treatment delivery.
CONCLUSION: Flavopiridol achieves significant clinical activity in patients with relapsed CLL, including those with high-risk genomic features and bulky lymphadenopathy. Subsequent clinical trials should use the amended treatment schedule developed herein and prophylactic corticosteroids.

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Year:  2009        PMID: 19826119      PMCID: PMC2793044          DOI: 10.1200/JCO.2009.22.6944

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  32 in total

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Journal:  J Clin Oncol       Date:  2001-04-15       Impact factor: 44.544

3.  A phase II trial of the cyclin-dependent kinase inhibitor flavopiridol in patients with previously untreated stage IV non-small cell lung cancer.

Authors:  G I Shapiro; J G Supko; A Patterson; C Lynch; J Lucca; P F Zacarola; A Muzikansky; J J Wright; T J Lynch; B J Rollins
Journal:  Clin Cancer Res       Date:  2001-06       Impact factor: 12.531

4.  Therapeutic role of alemtuzumab (Campath-1H) in patients who have failed fludarabine: results of a large international study.

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5.  Inhibition of CDKs as a therapeutic modality.

Authors:  E A Sausville; J Johnson; M Alley; D Zaharevitz; A M Senderowicz
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6.  Protein kinase inhibitors flavopiridol and 7-hydroxy-staurosporine down-regulate antiapoptosis proteins in B-cell chronic lymphocytic leukemia.

Authors:  S Kitada; J M Zapata; M Andreeff; J C Reed
Journal:  Blood       Date:  2000-07-15       Impact factor: 22.113

7.  Phase I study of the cyclin-dependent kinase inhibitor flavopiridol in combination with paclitaxel in patients with advanced solid tumors.

Authors:  Gary K Schwartz; Eileen O'Reilly; David Ilson; Leonard Saltz; Sunil Sharma; William Tong; Peter Maslak; Maxine Stoltz; Larry Eden; Pam Perkins; Sandra Endres; John Barazzoul; David Spriggs; David Kelsen
Journal:  J Clin Oncol       Date:  2002-04-15       Impact factor: 44.544

8.  Phase II study of the cyclin-dependent kinase inhibitor flavopiridol administered to patients with advanced gastric carcinoma.

Authors:  G K Schwartz; D Ilson; L Saltz; E O'Reilly; W Tong; P Maslak; J Werner; P Perkins; M Stoltz; D Kelsen
Journal:  J Clin Oncol       Date:  2001-04-01       Impact factor: 44.544

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

Authors:  Mitch A Phelps; Thomas S Lin; Amy J Johnson; Eunju Hurh; Darlene M Rozewski; Katherine L Farley; Di Wu; Kristie A Blum; Beth Fischer; Sarah M Mitchell; Mollie E Moran; Michelle Brooker-McEldowney; Nyla A Heerema; David Jarjoura; Larry J Schaaf; John C Byrd; Michael R Grever; James T Dalton
Journal:  Blood       Date:  2008-11-03       Impact factor: 22.113

10.  Flavopiridol induces apoptosis in chronic lymphocytic leukemia cells via activation of caspase-3 without evidence of bcl-2 modulation or dependence on functional p53.

Authors:  J C Byrd; C Shinn; J K Waselenko; E J Fuchs; T A Lehman; P L Nguyen; I W Flinn; L F Diehl; E Sausville; M R Grever
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6.  Flavopiridol treatment of patients aged 70 or older with refractory or relapsed chronic lymphocytic leukemia is a feasible and active therapeutic approach.

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Review 7.  Inhibiting CDK in Cancer Therapy: Current Evidence and Future Directions.

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Review 8.  Small Molecule Inhibitors in Chronic Lymphocytic Lymphoma and B Cell Non-Hodgkin Lymphoma.

Authors:  Allison Rosenthal
Journal:  Curr Hematol Malig Rep       Date:  2017-06       Impact factor: 3.952

Review 9.  The potential of venetoclax (ABT-199) in chronic lymphocytic leukemia.

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Journal:  Ther Adv Hematol       Date:  2016-07-08

10.  Flavopiridol, fludarabine, and rituximab in mantle cell lymphoma and indolent B-cell lymphoproliferative disorders.

Authors:  Thomas S Lin; Kristie A Blum; Diane Beth Fischer; Sarah M Mitchell; Amy S Ruppert; Pierluigi Porcu; Eric H Kraut; Robert A Baiocchi; Mollie E Moran; Amy J Johnson; Larry J Schaaf; Michael R Grever; John C Byrd
Journal:  J Clin Oncol       Date:  2009-12-14       Impact factor: 44.544

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