LPL gene expression is associated with poor prognosis in CLL and closely related to NOTCH1 mutations. (17th December 2015)

• Record Type: Journal Article
• Authors: Kristensen, Louise; Kristensen, Thomas; Abildgaard, Niels; Royo, Cristina; Frederiksen, Mikael; Mourits‐Andersen, Torben; Campo, Elias; Møller, Michael Boe
• Is Part Of: European journal of haematology. Volume 97:Number 2(2016:Aug.)
• Page Start: 175
• Page End: 182
• Publication Date: 2015-12-17
• Subjects: chronic lymphocytic leukemia -- LPL gene expression -- NOTCH1 mutations -- prognosis; Hematology -- Periodicals; Blood -- Diseases -- Periodicals; Blood -- Periodicals; 616.15005
• DOI: 10.1111/ejh.12700
• Languages: English
• ISSNs: 0902-4441

Abstract

Abstract: Introduction: Chronic lymphocytic leukemia is a heterogeneous yet incurable disease. Whole‐genome and whole‐exome sequencing studies have revealed recurrently occurring somatic mutations in some genes. Several other prognostic markers have previously been tested for their prognostic value in CLL. LPL is among these markers. Aim: To evaluate LPL gene expression together with the well‐established prognostic markers of CLL and investigate correlations with more recently identified prognostic markers, NOTCH1 and TP53 mutations. Methods: On 149 patients, LPL gene expression was analyzed by real‐time RT‐PCR. Exon 34 of NOTCH1 was PCR‐amplified and directly sequenced. Results: LPL gene expression could be measured as a categorical variable ( LPL +/ LPL ‐) and was associated with time to treatment ( P < 0.001) and overall survival ( P = 0.007). In patients otherwise classified as having a good prognosis according to established and new prognostic markers, 3 of 4 patients, who received treatment within 24 months after diagnosis, were LPL + ( P = 0.03). There was a strong correlation between NOTCH1 mutation and LPL + ( P = 0.005). The unfavorable prognosis of LPL + was maintained in CLL with wild‐type NOTCH1 . Conclusions: NOTCH1 mutations are tightly associated with LPL gene expression. LPL expression is independently associated with poor outcome in CLL and can be measured as a categorical variable.