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International prognostic score for asymptomatic early-stage chronic lymphocytic leukemia.
Condoluci, Adalgisa; Terzi di Bergamo, Lodovico; Langerbeins, Petra; Hoechstetter, Manuela A; Herling, Carmen D; De Paoli, Lorenzo; Delgado, Julio; Rabe, Kari G; Gentile, Massimo; Doubek, Michael; Mauro, Francesca R; Chiodin, Giorgia; Mattsson, Mattias; Bahlo, Jasmin; Cutrona, Giovanna; Kotaskova, Jana; Deambrogi, Clara; Smedby, Karin E; Spina, Valeria; Bruscaggin, Alessio; Wu, Wei; Moia, Riccardo; Bianchi, Elena; Gerber, Bernhard; Zucca, Emanuele; Gillessen, Silke; Ghielmini, Michele; Cavalli, Franco; Stussi, Georg; Hess, Mark A; Baumann, Tycho S; Neri, Antonino; Ferrarini, Manlio; Rosenquist, Richard; Forconi, Francesco; Foà, Robin; Pospisilova, Sarka; Morabito, Fortunato; Stilgenbauer, Stephan; Döhner, Hartmut; Parikh, Sameer A; Wierda, William G; Montserrat, Emili; Gaidano, Gianluca; Hallek, Michael; Rossi, Davide.
Afiliação
  • Condoluci A; Institute of Oncology Research, Università della Svizzera Italiana, Bellinzona, Switzerland.
  • Terzi di Bergamo L; Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
  • Langerbeins P; Institute of Oncology Research, Università della Svizzera Italiana, Bellinzona, Switzerland.
  • Hoechstetter MA; Center of Integrated Oncology Cologne Bonn and German CLL Study Group, University of Cologne, Cologne, Germany.
  • Herling CD; Hospital Munich-Schwabing, German CLL Study Group, Munich, Germany.
  • De Paoli L; Center of Integrated Oncology Cologne Bonn and German CLL Study Group, University of Cologne, Cologne, Germany.
  • Delgado J; Division of Hematology, Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.
  • Rabe KG; Hospital Clinic, Barcelona, Spain.
  • Gentile M; Mayo Clinic, Rochester, MN.
  • Doubek M; Azienda Ospedaliera of Cosenza, Cosenza, Italy.
  • Mauro FR; Interní Hematologická a Onkologická Klinika (IHOK), University Hospital Brno and Medical Faculty, Masaryk University, Brno, Czech Republic.
  • Chiodin G; Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
  • Mattsson M; Division of Hematology, Sapienza University, Rome, Italy.
  • Bahlo J; Cancer Sciences Division, University of Southampton, Southampton, United Kingdom.
  • Cutrona G; Uppsala University Hospital, Uppsala, Sweden.
  • Kotaskova J; Center of Integrated Oncology Cologne Bonn and German CLL Study Group, University of Cologne, Cologne, Germany.
  • Deambrogi C; IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
  • Smedby KE; Interní Hematologická a Onkologická Klinika (IHOK), University Hospital Brno and Medical Faculty, Masaryk University, Brno, Czech Republic.
  • Spina V; Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
  • Bruscaggin A; Division of Hematology, Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.
  • Wu W; Karolinska Institute, Stockholm, Sweden.
  • Moia R; Institute of Oncology Research, Università della Svizzera Italiana, Bellinzona, Switzerland.
  • Bianchi E; Institute of Oncology Research, Università della Svizzera Italiana, Bellinzona, Switzerland.
  • Gerber B; Institute of Oncology Research, Università della Svizzera Italiana, Bellinzona, Switzerland.
  • Zucca E; The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Nanjing, China.
  • Gillessen S; Division of Hematology, Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.
  • Ghielmini M; Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
  • Cavalli F; Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
  • Stussi G; Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
  • Hess MA; Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
  • Baumann TS; Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
  • Neri A; Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
  • Ferrarini M; Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
  • Rosenquist R; University of Texas MD Anderson Cancer Center, Houston, TX.
  • Forconi F; Hospital Clinic, Barcelona, Spain.
  • Foà R; Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
  • Pospisilova S; Department of Experimental Medicine, University of Genoa, Genoa, Italy.
  • Morabito F; Karolinska Institute, Stockholm, Sweden.
  • Stilgenbauer S; Cancer Sciences Division, University of Southampton, Southampton, United Kingdom.
  • Döhner H; Southampton University Hospital Trust, Southampton, United Kingdom.
  • Parikh SA; Division of Hematology, Sapienza University, Rome, Italy.
  • Wierda WG; Interní Hematologická a Onkologická Klinika (IHOK), University Hospital Brno and Medical Faculty, Masaryk University, Brno, Czech Republic.
  • Montserrat E; Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
  • Gaidano G; Biotechnology Research Unit Aprigliano, Cosenza, Italy.
  • Hallek M; Augusta Victoria Hospital, Jerusalem, Israel.
  • Rossi D; Department of Internal Medicine III, University Hospital of Ulm, Ulm, Germany; and.
Blood ; 135(21): 1859-1869, 2020 05 21.
Article em En | MEDLINE | ID: mdl-32267500
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Biomarcadores Tumorais / Ensaios Clínicos como Assunto / Nomogramas / Mutação Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Revista: Blood Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Biomarcadores Tumorais / Ensaios Clínicos como Assunto / Nomogramas / Mutação Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Revista: Blood Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Suíça