Detailed Information on Publication Record
2017
Chronic lymphocytic leukemia: A prognostic model comprising only two biomarkers (IGHV mutational status and FISH cytogenetics) separates patients with different outcome and simplifies the CLL-IPI
DELGADO, Julio, Michael DOUBEK, Tycho BAUMANN, Jana KOTAŠKOVÁ, Stefano MOLICA et. al.Basic information
Original name
Chronic lymphocytic leukemia: A prognostic model comprising only two biomarkers (IGHV mutational status and FISH cytogenetics) separates patients with different outcome and simplifies the CLL-IPI
Authors
DELGADO, Julio (724 Spain), Michael DOUBEK (203 Czech Republic, belonging to the institution), Tycho BAUMANN (724 Spain), Jana KOTAŠKOVÁ (203 Czech Republic, belonging to the institution), Stefano MOLICA (380 Italy), Pablo MOZAS (724 Spain), Alfredo RIVAS-DELGADO (724 Spain), Fortunato MORABITO (380 Italy), Šárka POSPÍŠILOVÁ (203 Czech Republic, guarantor, belonging to the institution) and Emili MONTSERRAT (724 Spain)
Edition
American Journal of Hematology, Hoboken, John Wiley & Sons, 2017, 0361-8609
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30200 3.2 Clinical medicine
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 5.303
RIV identification code
RIV/00216224:14740/17:00095652
Organization unit
Central European Institute of Technology
UT WoS
000399299300022
Keywords in English
INDEPENDENT PREDICTOR; MULTIVARIATE-ANALYSIS; GENOMIC ABERRATIONS; SURVIVAL ANALYSIS; CD38 EXPRESSION; DOUBLING TIME; 1ST TREATMENT; TRIAL; INDEX; GENE
Tags
Tags
International impact, Reviewed
Změněno: 28/2/2018 16:18, Mgr. Pavla Foltynová, Ph.D.
Abstract
V originále
Rai and Binet staging systems are important to predict the outcome of patients with chronic lymphocytic leukemia (CLL) but do not reflect the biologic diversity of the disease nor predict response to therapy, which ultimately shape patients' outcome. We devised a biomarkers-only CLL prognostic system based on the two most important prognostic parameters in CLL (i.e., IGHV mutational status and fluorescence in situ hybridization [FISH] cytogenetics), separating three different risk groups: (1) low-risk (mutated IGHV+no adverse FISH cytogenetics [del(17p), del(11q)]); (2) intermediate-risk (either unmutated IGHV or adverse FISH cytogenetics) and (3) high-risk (unmutated IGHV+adverse FISH cytogenetics). In 524 unselected subjects with CLL, the 10-year overall survival was 82% (95% CI 76%-88%), 52% (45%-62%), and 27% (17%-42%) for the low-, intermediate-, and high-risk groups, respectively. Patients with low-risk comprised around 50% of the series and had a life expectancy comparable to the general population. The prognostic model was fully validated in two independent cohorts, including 417 patients representative of general CLL population and 337 patients with Binet stage A CLL. The model had a similar discriminatory value as the CLL-IPI. Moreover, it applied to all patients with CLL independently of age, and separated patients with different risk within Rai or Binet clinical stages. The biomarkers-only CLL prognostic system presented here simplifies the CLL-IPI and could be useful in daily practice and to stratify patients in clinical trials.
Links
LQ1601, research and development project |
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NV15-30015A, research and development project |
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NV15-31834A, research and development project |
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