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.Základní údaje
Originální název
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
Autoři
DELGADO, Julio (724 Španělsko), Michael DOUBEK (203 Česká republika, domácí), Tycho BAUMANN (724 Španělsko), Jana KOTAŠKOVÁ (203 Česká republika, domácí), Stefano MOLICA (380 Itálie), Pablo MOZAS (724 Španělsko), Alfredo RIVAS-DELGADO (724 Španělsko), Fortunato MORABITO (380 Itálie), Šárka POSPÍŠILOVÁ (203 Česká republika, garant, domácí) a Emili MONTSERRAT (724 Španělsko)
Vydání
American Journal of Hematology, Hoboken, John Wiley & Sons, 2017, 0361-8609
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30200 3.2 Clinical medicine
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 5.303
Kód RIV
RIV/00216224:14740/17:00095652
Organizační jednotka
Středoevropský technologický institut
UT WoS
000399299300022
EID Scopus
2-s2.0-85012996204
Klíčová slova anglicky
INDEPENDENT PREDICTOR; MULTIVARIATE-ANALYSIS; GENOMIC ABERRATIONS; SURVIVAL ANALYSIS; CD38 EXPRESSION; DOUBLING TIME; 1ST TREATMENT; TRIAL; INDEX; GENE
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 28. 2. 2018 16:18, Mgr. Pavla Foltynová, Ph.D.
Anotace
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.
Návaznosti
LQ1601, projekt VaV |
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NV15-30015A, projekt VaV |
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NV15-31834A, projekt VaV |
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