International prognostic score for asymptomatic early-stage chronic lymphocytic leukemia.


Journal

Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509

Informations de publication

Date de publication:
21 05 2020
Historique:
received: 23 09 2019
accepted: 12 02 2020
pubmed: 9 4 2020
medline: 10 2 2021
entrez: 9 4 2020
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 32267500
pii: S0006-4971(20)62013-4
doi: 10.1182/blood.2019003453
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1859-1869

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2020 by The American Society of Hematology.

Auteurs

Adalgisa Condoluci (A)

Institute of Oncology Research, Università della Svizzera Italiana, Bellinzona, Switzerland.
Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

Lodovico Terzi di Bergamo (L)

Institute of Oncology Research, Università della Svizzera Italiana, Bellinzona, Switzerland.

Petra Langerbeins (P)

Center of Integrated Oncology Cologne Bonn and German CLL Study Group, University of Cologne, Cologne, Germany.

Manuela A Hoechstetter (MA)

Hospital Munich-Schwabing, German CLL Study Group, Munich, Germany.

Carmen D Herling (CD)

Center of Integrated Oncology Cologne Bonn and German CLL Study Group, University of Cologne, Cologne, Germany.

Lorenzo De Paoli (L)

Division of Hematology, Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.

Julio Delgado (J)

Hospital Clinic, Barcelona, Spain.

Kari G Rabe (KG)

Mayo Clinic, Rochester, MN.

Massimo Gentile (M)

Azienda Ospedaliera of Cosenza, Cosenza, Italy.

Michael Doubek (M)

Interní Hematologická a Onkologická Klinika (IHOK), University Hospital Brno and Medical Faculty, Masaryk University, Brno, Czech Republic.
Central European Institute of Technology, Masaryk University, Brno, Czech Republic.

Francesca R Mauro (FR)

Division of Hematology, Sapienza University, Rome, Italy.

Giorgia Chiodin (G)

Cancer Sciences Division, University of Southampton, Southampton, United Kingdom.

Mattias Mattsson (M)

Uppsala University Hospital, Uppsala, Sweden.

Jasmin Bahlo (J)

Center of Integrated Oncology Cologne Bonn and German CLL Study Group, University of Cologne, Cologne, Germany.

Giovanna Cutrona (G)

IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Jana Kotaskova (J)

Interní Hematologická a Onkologická Klinika (IHOK), University Hospital Brno and Medical Faculty, Masaryk University, Brno, Czech Republic.
Central European Institute of Technology, Masaryk University, Brno, Czech Republic.

Clara Deambrogi (C)

Division of Hematology, Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.

Karin E Smedby (KE)

Karolinska Institute, Stockholm, Sweden.

Valeria Spina (V)

Institute of Oncology Research, Università della Svizzera Italiana, Bellinzona, Switzerland.

Alessio Bruscaggin (A)

Institute of Oncology Research, Università della Svizzera Italiana, Bellinzona, Switzerland.

Wei Wu (W)

Institute of Oncology Research, Università della Svizzera Italiana, Bellinzona, Switzerland.
The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Nanjing, China.

Riccardo Moia (R)

Division of Hematology, Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.

Elena Bianchi (E)

Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

Bernhard Gerber (B)

Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

Emanuele Zucca (E)

Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

Silke Gillessen (S)

Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

Michele Ghielmini (M)

Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

Franco Cavalli (F)

Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

Georg Stussi (G)

Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

Mark A Hess (MA)

University of Texas MD Anderson Cancer Center, Houston, TX.

Tycho S Baumann (TS)

Hospital Clinic, Barcelona, Spain.

Antonino Neri (A)

Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.

Manlio Ferrarini (M)

Department of Experimental Medicine, University of Genoa, Genoa, Italy.

Richard Rosenquist (R)

Karolinska Institute, Stockholm, Sweden.

Francesco Forconi (F)

Cancer Sciences Division, University of Southampton, Southampton, United Kingdom.
Southampton University Hospital Trust, Southampton, United Kingdom.

Robin Foà (R)

Division of Hematology, Sapienza University, Rome, Italy.

Sarka Pospisilova (S)

Interní Hematologická a Onkologická Klinika (IHOK), University Hospital Brno and Medical Faculty, Masaryk University, Brno, Czech Republic.
Central European Institute of Technology, Masaryk University, Brno, Czech Republic.

Fortunato Morabito (F)

Biotechnology Research Unit Aprigliano, Cosenza, Italy.
Augusta Victoria Hospital, Jerusalem, Israel.

Stephan Stilgenbauer (S)

Department of Internal Medicine III, University Hospital of Ulm, Ulm, Germany; and.

Hartmut Döhner (H)

Department of Internal Medicine III, University Hospital of Ulm, Ulm, Germany; and.

Sameer A Parikh (SA)

Mayo Clinic, Rochester, MN.

William G Wierda (WG)

University of Texas MD Anderson Cancer Center, Houston, TX.

Emili Montserrat (E)

Hospital Clinic, Barcelona, Spain.
Institute of Hematology and Oncology, University of Barcelona, Barcelona, Spain.

Gianluca Gaidano (G)

Division of Hematology, Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.

Michael Hallek (M)

Center of Integrated Oncology Cologne Bonn and German CLL Study Group, University of Cologne, Cologne, Germany.

Davide Rossi (D)

Institute of Oncology Research, Università della Svizzera Italiana, Bellinzona, Switzerland.
Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

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