TY - JOUR
T1 - Elevated lactate dehydrogenase has prognostic relevance in treatment-naïve patients affected by chronic lymphocytic leukemia with trisomy 12
AU - Autore, Francesco
AU - Strati, Paolo
AU - Innocenti, Idanna
AU - Corrente, Francesco
AU - Trentin, Livio
AU - Cortelezzi, Agostino
AU - Visco, Carlo
AU - Coscia, Marta
AU - Cuneo, Antonio
AU - Gozzetti, Alessandro
AU - Mauro, Francesca Romana
AU - Frustaci, Anna Maria
AU - Gentile, Massimo
AU - Morabito, Fortunato
AU - Molica, Stefano
AU - Falcucci, Paolo
AU - D’Arena, Giovanni
AU - Murru, Roberta
AU - Vincelli, Donatella
AU - Efremov, Dimitar G.
AU - Ferretti, Antonietta
AU - Rigolin, Gian Matteo
AU - Vitale, Candida
AU - Tisi, Maria Chiara
AU - Reda, Gianluigi
AU - Visentin, Andrea
AU - Sica, Simona
AU - Foà, Robin
AU - Ferrajoli, Alessandra
AU - Laurenti, Luca
PY - 2019
Y1 - 2019
N2 - 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.
AB - 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.
KW - CLL
KW - LDH
KW - Prognosis
KW - Trisomy 12
KW - CLL
KW - LDH
KW - Prognosis
KW - Trisomy 12
UR - http://hdl.handle.net/10807/140461
UR - https://www.mdpi.com/2072-6694/11/7/896/pdf
U2 - 10.3390/cancers11070896
DO - 10.3390/cancers11070896
M3 - Article
SN - 2072-6694
VL - 11
SP - 896
EP - 896
JO - Cancers
JF - Cancers
ER -