| Literature DB >> 24705492 |
Paolo Strati1, Michael J Keating1, Susan M O'Brien1, Jan Burger1, Alessandra Ferrajoli1, Nitin Jain1, Francesco Paolo Tambaro2, Zeev Estrov1, Jeffrey Jorgensen3, Pramoda Challagundla3, Stefan H Faderl1, William G Wierda1.
Abstract
The high complete remission rate with first-line combined fludarabine, cyclophosphamide, and rituximab (FCR) begs the question of the value of minimal residual disease (MRD)-negative status as a treatment end point. We report on 237 patients with chronic lymphocytic leukemia who received first-line FCR. MRD was prospectively assessed by 4-color flow cytometry in bone marrow after course 3 and at final response assessment. After course 3 and at final response assessment, 17% and 43% of patients were MRD negative in bone marrow, respectively. A mutated immunoglobulin heavy chain variable gene and trisomy 12 were independently associated with MRD-negative status both after 3 courses of FCR and at final response assessment in multivariable analyses (MVAs). MRD-negative status was independently associated with significantly longer progression-free survival (PFS) and overall survival (OS) in MVA (P = .03 and .02, respectively). This association was confirmed also on landmark MVA at the time of MRD assessment (P = .04 and .05, respectively). MRD-negative patients had comparable PFS and OS, independent of the number of courses received or interim staging. Early MRD eradication may be a desirable goal, prompting consideration of early discontinuation of treatment. This trial was registered at www.clinicaltrials.gov as #NCT00759798.Entities:
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Year: 2014 PMID: 24705492 PMCID: PMC4067501 DOI: 10.1182/blood-2013-11-538116
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113