| Literature DB >> 32042081 |
Hartmut Döhner1, Stephan Stilgenbauer1, Michael Hallek2, Manuela A Hoechstetter3, Raymonde Busch4, Barbara Eichhorst5, Andreas Bühler6, Dirk Winkler6, Jasmin Bahlo5, Sandra Robrecht5, Michael J Eckart7, Ursula Vehling-Kaiser8, Georg Jacobs9, Ulrich Jäger10, Hans Jürgen Hurtz11, Georg Hopfinger12, Frank Hartmann13, Harald Fuss14, Wolfgang Abenhardt15, Ilona Blau16, Werner Freier17, Lothar Müller18, Maria Goebeler19, Clemens Wendtner3,5, Kirsten Fischer5, Carmen D Herling5, Michael Starck3, Martin Bentz20, Bertold Emmerich21.
Abstract
The heterogeneity of early stage CLL challenges prognostication, and refinement of prognostic indices for risk-adapted management in this population is essential. The aim of the multicenter, prospective CLL1 trial was to explore a novel prognostic model (CLL1-PM) developed to identify risk groups, separating patients with favorable from others with dismal prognosis. A cohort of 539 clinically, biochemically, and genetically characterized Binet stage A patients were observed until progression, first-line treatment, or death. Multivariate analysis identified six independent factors associated with overall survival (OS) and time-to-first treatment (TTFT): del(17p), unmutated IGHV, del(11q), ß2-microglobulin >3.5 mg/dL, lymphocyte doubling time (LDT) <12 months, and age >60 years. These factors were integrated into the CLL1-PM, which stratified patients into four risk groups. The CLL1-PM was prognostic for OS and TTFT, e.g., the risk of treatment at 5 years was 85.9, 51.8, 27.6, and 11.3% for very low (0-1.5), low (2-4), high (4.5-6.5), and very high-risk (7-14) scores, respectively (P < 0.001). Notably, in addition to factors comprising CLL-IPI, we substantiated del(11q) and LDT as prognostic factors in early CLL. Altogether, our findings would be useful to effectively stratify Binet stage A patients, particularly within the scope of clinical trials evaluating novel agents.Entities:
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Year: 2020 PMID: 32042081 DOI: 10.1038/s41375-020-0727-y
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528