Elevated lactate dehydrogenase has prognostic relevance in treatment-naïve patients affected by chronic lymphocytic leukemia with trisomy 12
Articolo
Data di Pubblicazione:
2019
Abstract:
Chronic Lymphocytic Leukemia (CLL) patients with +12 have been reported to have specific clinical and biologic features. We performed an analysis of the association between demographic; clinical; laboratory; biologic features and outcome in CLL patients with +12 to identify parameters predictive of disease progression; time to treatment; and survival. The study included 487 treatment-naive CLL patients with +12 from 15 academic centers; diagnosed between January 2000 and July 2016; and 816 treatment-naïve patients with absence of Fluorescence In Situ Hybridization (FISH) abnormalities. A cohort of 250 patients with +12 CLL followed at a single US institution was used for external validation. In patients with +12; parameters associated with worse prognosis in the multivariate model were high Lactate DeHydrogenase (LDH) and β-2- microglobulin and unmutated immunoglobulin heavy-chain variable region gene (IGHV). CLL patients with +12 and high LDH levels showed a shorter Progression-Free-Survival (PFS) (30 months vs. 65 months; p < 0.001), Treatment-Free-Survival (TFS) (33 months vs. 69 months; p < 0.001), Overall Survival (OS) (131 months vs. 181 months; p < 0.001) and greater CLL-related mortality (29% vs. 11% at 10 years; p < 0.001) when compared with +12 CLL patients with normal LDH levels. The same differences were observed in the validation cohort. These data suggest that serum LDH levels can predict PFS; TFS; OS and CLL-specific survival in CLL patients with +12.
Tipologia CRIS:
03A-Articolo su Rivista
Keywords:
CLL; LDH; Prognosis; Trisomy 12
Elenco autori:
Autore F.; Strati P.; Innocenti I.; Corrente F.; Trentin L.; Cortelezzi A.; Visco C.; Coscia M.; Cuneo A.; Gozzetti A.; Mauro F.R.; Frustaci A.M.; Gentile M.; Morabito F.; Molica S.; Falcucci P.; D'Arena G.; Murru R.; Vincelli D.; Efremov D.G.; Ferretti A.; Rigolin G.M.; Vitale C.; Tisi M.C.; Reda G.; Visentin A.; Sica S.; Foa R.; Ferrajoli A.; Laurenti L.
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