| Literature DB >> 32267500 |
Adalgisa Condoluci1,2, Lodovico Terzi di Bergamo1, Petra Langerbeins3, Manuela A Hoechstetter4, Carmen D Herling3, Lorenzo De Paoli5, Julio Delgado6, Kari G Rabe7, Massimo Gentile8, Michael Doubek9,10, Francesca R Mauro11, Giorgia Chiodin12, Mattias Mattsson13, Jasmin Bahlo3, Giovanna Cutrona14, Jana Kotaskova9,10, Clara Deambrogi5, Karin E Smedby15, Valeria Spina1, Alessio Bruscaggin1, Wei Wu1,16, Riccardo Moia5, Elena Bianchi2, Bernhard Gerber2, Emanuele Zucca2, Silke Gillessen2, Michele Ghielmini2, Franco Cavalli2, Georg Stussi2, Mark A Hess17, Tycho S Baumann6, Antonino Neri18, Manlio Ferrarini19, Richard Rosenquist15, Francesco Forconi12,20, Robin Foà11, Sarka Pospisilova9,10, Fortunato Morabito21,22, Stephan Stilgenbauer23, Hartmut Döhner23, Sameer A Parikh7, William G Wierda17, Emili Montserrat6,24, Gianluca Gaidano5, Michael Hallek3, Davide Rossi1,2.
Abstract
Most patients with chronic lymphocytic leukemia (CLL) are diagnosed with early-stage disease and managed with active surveillance. The individual course of patients with early-stage CLL is heterogeneous, and their probability of needing treatment is hardly anticipated at diagnosis. We aimed at developing an international prognostic score to predict time to first treatment (TTFT) in patients with CLL with early, asymptomatic disease (International Prognostic Score for Early-stage CLL [IPS-E]). Individual patient data from 11 international cohorts of patients with early-stage CLL (n = 4933) were analyzed to build and validate the prognostic score. Three covariates were consistently and independently correlated with TTFT: unmutated immunoglobulin heavy variable gene (IGHV), absolute lymphocyte count higher than 15 × 109/L, and presence of palpable lymph nodes. The IPS-E was the sum of the covariates (1 point each), and separated low-risk (score 0), intermediate-risk (score 1), and high-risk (score 2-3) patients showing a distinct TTFT. The score accuracy was validated in 9 cohorts staged by the Binet system and 1 cohort staged by the Rai system. The C-index was 0.74 in the training series and 0.70 in the aggregate of validation series. By meta-analysis of the training and validation cohorts, the 5-year cumulative risk for treatment start was 8.4%, 28.4%, and 61.2% among low-risk, intermediate-risk, and high-risk patients, respectively. The IPS-E is a simple and robust prognostic model that predicts the likelihood of treatment requirement in patients with early-stage CLL. The IPS-E can be useful in clinical management and in the design of early intervention clinical trials.Entities:
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Year: 2020 PMID: 32267500 DOI: 10.1182/blood.2019003453
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113