| Literature DB >> 27750483 |
Matthew D Seftel1, John Kuruvilla2, Tom Kouroukis3, Versha Banerji1, Graeme Fraser3, Michael Crump2, Rajat Kumar1, Haji I Chalchal4,5, Muhammad Salim4,5, Rob C Laister2, Susan Crocker6, Spencer B Gibson7, Marcia Toguchi8, John F Lyons8, Hao Xu9, Jean Powers9, Joana Sederias9, Lesley Seymour9, Annette E Hay9,10.
Abstract
AT7519M is a small molecule inhibitor of cyclin-dependent kinases 1, 2, 4, 5, and 9 with in vitro activity against lymphoid malignancies. In two concurrent Phase II trials, we evaluated AT7519M in relapsed or refractory chronic lymphocytic leukemia (CLL) and mantle cell lymphoma (MCL) using the recommended Phase II dosing of 27 mg/m2 twice weekly for 2 of every 3 weeks. Primary objective was objective response rate (ORR). Nineteen patients were accrued (7 CLL, 12 MCL). Four CLL patients achieved stable disease (SD). Two MCL patients achieved partial response (PR), and 6 had SD. One additional MCL patient with SD subsequently achieved PR 9 months after completion of AT7519M. Tumor lysis syndrome was not reported. In conclusion, AT7519M was safely administered to patients with relapsed/refractory CLL and MCL. In CLL, some patients had tumor reductions, but the ORR was low. In MCL, activity was noted with ORR of 27%.Entities:
Keywords: Chronic lymphocytic leukemia; cyclin-dependent kinase inhibitors; mantle cell lymphoma
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Year: 2016 PMID: 27750483 DOI: 10.1080/10428194.2016.1239259
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022