2015
Analysis of Prognostic Significance of Merkel Cell Polyomavirus in Chronic Lymphocytic Leukemia
TRIZULJAK, Jakub, Josef SROVNAL, Karla PLEVOVÁ, Yvona BRYCHTOVÁ, Lukáš SEMERÁD et. al.Základní údaje
Originální název
Analysis of Prognostic Significance of Merkel Cell Polyomavirus in Chronic Lymphocytic Leukemia
Autoři
TRIZULJAK, Jakub (703 Slovensko, garant, domácí), Josef SROVNAL (203 Česká republika), Karla PLEVOVÁ (203 Česká republika, domácí), Yvona BRYCHTOVÁ (203 Česká republika, domácí), Lukáš SEMERÁD (203 Česká republika, domácí), Denisa BAKEŠOVÁ (703 Slovensko, domácí), Eva LÉTALOVÁ (203 Česká republika, domácí), Andrea BENEDÍKOVÁ (203 Česká republika), Jiří MAYER (203 Česká republika, domácí), Marian HAJDÚCH (203 Česká republika), Šárka POSPÍŠILOVÁ (203 Česká republika, domácí) a Michael DOUBEK (203 Česká republika, domácí)
Vydání
Clinical Lymphoma Myeloma & Leukemia, Dallas, Cig Media Group, 2015, 2152-2650
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: 2.316
Kód RIV
RIV/00216224:14110/15:00083517
Organizační jednotka
Lékařská fakulta
UT WoS
000357967700010
Klíčová slova anglicky
Chronic lymphocytic leukemia; Merkel cell polyomavirus; Overall survival; Polymerase chain reaction; Prognostic factors
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 28. 4. 2016 13:51, Ing. Mgr. Věra Pospíšilíková
Anotace
V originále
Merkel cell polyomavirus (MCPyV) has been found to be associated with chronic lymphocytic leukemia (CLL). We evaluated its prognostic significance in CLL. MCPyV occurrence seems to be a relatively rare event during the course of CLL. MCPyV is also unlikely to influence the outcome of CLL patients. Background: Merkel cell polyomavirus (MCPyV), a ubiquitous DNA tumor virus, has been found to be associated with Merkel cell carcinoma and chronic lymphocytic leukemia (CLL). Previous studies have reported conflicting results on the frequency and potential pathogenetic role of MCPyV in CLL. The aim of this study was to evaluate MCPyV's association with CLL and its prognostic significance. Patients and Methods: Between 2006 and 2013, DNA samples obtained from CLL patients (n = 119) before treatment were tested for MCPyV using quantitative real-time polymerase chain reaction analysis and verified by gel electrophoresis. Only samples testing positive by both methods were considered valid. Results: We found that 13 (11%) of 119 CLL cases were positive for MCPyV. Between the groups of MCPyV-positive and -negative patients, there was no significant difference in the sex, age, cytogenetics, presence of p53 defect, or immunoglobulin heavy chain (IGHV) mutational status. In the subset of MCPyV-negative patients, advanced Rai stage (III to IV) was found more frequently, and therapy was initiated more often. There was no difference in overall response rate, median progression-free survival, and overall survival between both groups. We did not observe any new positivity after treatment in initially MCPyV-negative patients. Conclusion: This study provides the first analysis of the prognostic role of MCPyV in CLL. MCPyV occurrence seems to be a relatively rare event during the course of CLL. MCPyV is also unlikely to influence the outcome of CLL patients.
Návaznosti
ED1.1.00/02.0068, projekt VaV |
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EE2.3.20.0045, projekt VaV |
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NT13493, projekt VaV |
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7E13008, projekt VaV |
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