Detail
Článek
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Improving risk-stratification of patients with chronic lymphocytic leukemia using multivariate patient similarity networks

P. Turcsanyi, E. Kriegova, M. Kudelka, M. Radvansky, L. Kruzova, R. Urbanova, P. Schneiderova, H. Urbankova, T. Papajik,

. 2019 ; 79 (-) : 60-68. [pub] 20190219

Jazyk angličtina Země Velká Británie

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc19044947

Grantová podpora
NV16-32339A MZ0 CEP - Centrální evidence projektů

BACKGROUND: Better risk-stratification of patients with chronic lymphocytic leukemia (CLL) and identification of subsets of ultra-high-risk (HR)-CLL patients are crucial in the contemporary era of an expanded therapeutic armamentarium for CLL. METHODS: A multivariate patient similarity network and clustering was applied to assess the prognostic values of routine genetic, laboratory, and clinical factors and to identify subsets of ultra-HR-CLL patients. The study cohort consisted of 116 HR-CLL patients (F/M 36/80, median age 63 yrs) carrying del(11q), del(17p)/TP53 mutations and/or complex karyotype (CK) at the time of diagnosis. RESULTS: Three major subsets based on the presence of key prognostic variables as genetic aberrations, bulky lymphadenopathy, splenomegaly, and gender: profile (P)-I (n = 34, men/women with CK + no del(17p)/TP53 mutations), P-II (n = 47, predominantly men with del(11q) + no CK + no del(17p)/TP53 mutations), and P-III (n = 35, men/women with del(17p)/TP53 mutations, with/without del(11q) and CK) were revealed. Subanalysis of major subsets identified three ultra-HR-CLL groups: men with TP53 disruption with/without CK, women with TP53 disruption with CK and men/women with CK + del(11q) with poor short-term outcomes (25% deaths/12 mo). Besides confirming the combinations of known risk-factors, the used patient similarity network added further refinement of subsets of HR-CLL patients who may profit from different targeted drugs. CONCLUSIONS: This study showed for the first time in hemato-oncology the usefulness of the multivariate patient similarity networks for stratification of HR-CLL patients. This approach shows the potential for clinical implementation of precision medicine, which is especially important in view of an armamentarium of novel targeted drugs.

000      
00000naa a2200000 a 4500
001      
bmc19044947
003      
CZ-PrNML
005      
20200526102448.0
007      
ta
008      
200109s2019 xxk f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.leukres.2019.02.005 $2 doi
035    __
$a (PubMed)30852300
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxk
100    1_
$a Turcsanyi, Peter $u Department of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Olomouc, Czech Republic. Electronic address: Peter.Turcsanyi@fnol.cz.
245    10
$a Improving risk-stratification of patients with chronic lymphocytic leukemia using multivariate patient similarity networks / $c P. Turcsanyi, E. Kriegova, M. Kudelka, M. Radvansky, L. Kruzova, R. Urbanova, P. Schneiderova, H. Urbankova, T. Papajik,
520    9_
$a BACKGROUND: Better risk-stratification of patients with chronic lymphocytic leukemia (CLL) and identification of subsets of ultra-high-risk (HR)-CLL patients are crucial in the contemporary era of an expanded therapeutic armamentarium for CLL. METHODS: A multivariate patient similarity network and clustering was applied to assess the prognostic values of routine genetic, laboratory, and clinical factors and to identify subsets of ultra-HR-CLL patients. The study cohort consisted of 116 HR-CLL patients (F/M 36/80, median age 63 yrs) carrying del(11q), del(17p)/TP53 mutations and/or complex karyotype (CK) at the time of diagnosis. RESULTS: Three major subsets based on the presence of key prognostic variables as genetic aberrations, bulky lymphadenopathy, splenomegaly, and gender: profile (P)-I (n = 34, men/women with CK + no del(17p)/TP53 mutations), P-II (n = 47, predominantly men with del(11q) + no CK + no del(17p)/TP53 mutations), and P-III (n = 35, men/women with del(17p)/TP53 mutations, with/without del(11q) and CK) were revealed. Subanalysis of major subsets identified three ultra-HR-CLL groups: men with TP53 disruption with/without CK, women with TP53 disruption with CK and men/women with CK + del(11q) with poor short-term outcomes (25% deaths/12 mo). Besides confirming the combinations of known risk-factors, the used patient similarity network added further refinement of subsets of HR-CLL patients who may profit from different targeted drugs. CONCLUSIONS: This study showed for the first time in hemato-oncology the usefulness of the multivariate patient similarity networks for stratification of HR-CLL patients. This approach shows the potential for clinical implementation of precision medicine, which is especially important in view of an armamentarium of novel targeted drugs.
650    _2
$a dospělí $7 D000328
650    _2
$a senioři $7 D000368
650    _2
$a senioři nad 80 let $7 D000369
650    _2
$a shluková analýza $7 D016000
650    _2
$a kohortové studie $7 D015331
650    _2
$a mutační analýza DNA $7 D004252
650    _2
$a rozhodovací stromy $7 D003663
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a lidé $7 D006801
650    _2
$a chronická lymfatická leukemie $x diagnóza $x epidemiologie $x genetika $x terapie $7 D015451
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a lidé středního věku $7 D008875
650    _2
$a multivariační analýza $7 D015999
650    _2
$a neuronové sítě (počítačové) $7 D016571
650    _2
$a individualizovaná medicína $x metody $7 D057285
650    _2
$a prediktivní hodnota testů $7 D011237
650    _2
$a prognóza $7 D011379
650    _2
$a hodnocení rizik $7 D018570
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Kriegova, Eva $u Department of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Czech Republic, Olomouc, Czech Republic. Electronic address: eva.kriegova@email.cz.
700    1_
$a Kudelka, Milos $u Department of Computer Science, Faculty of Electrical Engineering and Computer Science, VSB - Technical University of Ostrava, Ostrava, Czech Republic. Electronic address: Milos.Kudelka@vsb.cz.
700    1_
$a Radvansky, Martin $u Department of Computer Science, Faculty of Electrical Engineering and Computer Science, VSB - Technical University of Ostrava, Ostrava, Czech Republic. Electronic address: Martin.Radvansky@vsb.cz.
700    1_
$a Kruzova, Lenka $u Department of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Olomouc, Czech Republic. Electronic address: Lenka.Kruzova@fnol.cz.
700    1_
$a Urbanova, Renata $u Department of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Olomouc, Czech Republic. Electronic address: Renata.Urbanova@fnol.cz.
700    1_
$a Schneiderova, Petra $u Department of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Czech Republic, Olomouc, Czech Republic. Electronic address: Petra.Schneiderova@fnol.cz.
700    1_
$a Urbankova, Helena $u Department of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Olomouc, Czech Republic. Electronic address: Helena.Urbankova@fnol.cz.
700    1_
$a Papajik, Tomas $u Department of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Olomouc, Czech Republic. Electronic address: Tomas.Papajik@fnol.cz.
773    0_
$w MED00003141 $t Leukemia research $x 1873-5835 $g Roč. 79, č. - (2019), s. 60-68
856    41
$u https://pubmed.ncbi.nlm.nih.gov/30852300 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20200109 $b ABA008
991    __
$a 20200526102445 $b ABA008
999    __
$a ok $b bmc $g 1483216 $s 1083620
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2019 $b 79 $c - $d 60-68 $e 20190219 $i 1873-5835 $m Leukemia research $n Leuk Res $x MED00003141
GRA    __
$a NV16-32339A $p MZ0
LZP    __
$a Pubmed-20200109

Najít záznam

Citační ukazatele

Nahrávání dat...

Možnosti archivace

Nahrávání dat...