TP53 Mutation and Complex Karyotype Portends a Dismal Prognosis in Patients With Mantle Cell Lymphoma

The predictive value of TP53 mutation (TP53mut) and complex karyotype (CK) was analyzed in 74 mantle-cell lymphoma patients. CK and TP53mut were predictors of inferior progression-free and overall survival, independent of age and Mantle Cell Lymphoma International Prognostic Index. The combination o...

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Veröffentlicht in:Clinical lymphoma, myeloma and leukemia myeloma and leukemia, 2018-11, Vol.18 (11), p.762-768
Hauptverfasser: Obr, Aleš, Procházka, Vít, Jirkuvová, Andrea, Urbánková, Helena, Kriegova, Eva, Schneiderová, Petra, Vatolíková, Michaela, Papajík, Tomáš
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Sprache:eng
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Zusammenfassung:The predictive value of TP53 mutation (TP53mut) and complex karyotype (CK) was analyzed in 74 mantle-cell lymphoma patients. CK and TP53mut were predictors of inferior progression-free and overall survival, independent of age and Mantle Cell Lymphoma International Prognostic Index. The combination of TP53mut and CK status stratified the patient population into 3 prognostic groups (P < .001). In patients with TP53mut combined with a CK, an innovative therapy might be considered. TP53 mutation (TP53mut) and a complex karyotype (CK) were shown to be predictors of poor outcome in mantle-cell lymphoma (MCL). In this study we examined the combined effect of both of these risk factors. Patients diagnosed with MCL between January 2000 and December 2014 (n = 74) were evaluated. Forty-eight of them had available material for TP53 and cytogenetic examination. We analyzed the prognostic effect of combined TP53mut and CK in the cohort of patients treated with rituximab-containing therapy. Three-year (3-y) overall survival (OS) and 3-y progression-free survival (PFS) in CK patients were shorter compared with non-CK (P = .001 for OS; P = .02 for PFS). TP53mut was a predictor of shorter survival compared with TP53 wild type (OS and PFS; P < .001). The incidence of TP53mut was not significantly associated with CK (P = .240). CK and TP53mut were predictors of inferior PFS and OS independent of age and Mantle-Cell Lymphoma International Prognostic Index, with hazard ratios of 2.35 (P = .024), 4.50 (P < .001) for PFS and 4.31 (P < .001), 5.46 (P < .001) for OS analysis in the CK and TP53mut groups, respectively. The combination of TP53mut and CK status stratified the patients into 3 prognostic groups (P < .001) with the worst outcome in patients with CK and TP53mut. TP53 mutation and CK occurred independently and patients harboring both had a dismal prognosis. The study suggests the importance of molecular cytogenetics and examination of the TP53mut status to be performed simultaneously before treatment.
ISSN:2152-2650
2152-2669
DOI:10.1016/j.clml.2018.07.282