Back to Search Start Over

MYC protein is a high-risk factor in mantle cell lymphoma and identifies cases beyond morphology, proliferation and TP53/p53 : a Nordic Lymphoma Group study

Authors :
Rodrigues, Joana M.
Hollander, Peter
Schmidt, Lina
Gkika, Eirinaios
Razmara, Masoud
Kumar, Darshan
Geisler, Christian
Grønbæk, Kirsten
Eskelund, Christian W.
Räty, Riikka
Kolstad, Arne
Sundström, Christer
Glimelius, Ingrid
Porwit, Anna
Jerkeman, Mats
Ek, Sara
Rodrigues, Joana M.
Hollander, Peter
Schmidt, Lina
Gkika, Eirinaios
Razmara, Masoud
Kumar, Darshan
Geisler, Christian
Grønbæk, Kirsten
Eskelund, Christian W.
Räty, Riikka
Kolstad, Arne
Sundström, Christer
Glimelius, Ingrid
Porwit, Anna
Jerkeman, Mats
Ek, Sara
Publication Year :
2024

Abstract

The transcription factor MYC is a well-described oncogene with an important role in lymphomagenesis, but its significance for clinical outcome in mantle cell lymphoma (MCL) remains to be determined. We performed an investigation of the expression of MYC protein in a cohort of 251 MCL patients complemented by analyses of structural aberrations and mRNA, in a sub-cohort of patients. Fourteen percent (n=35) of patients showed high MYC protein expression with >20% positive cells (MYChigh), among whom only one translocation was identified, and 86% (n=216) of patients showed low MYC protein expression. Low copy number gains of MYC were detected in ten patients, but with no correlation to MYC protein levels. However, MYC mRNA levels correlated significantly to MYC protein levels with a R2 value of 0.76. Patients with a MYChigh tumor had both an independent inferior overall survival and an inferior progression-free survival (hazard ratio [HR]=2.03, 95% confidence interval [95% CI]: 1.2-3.4 and HR=2.2, 95% CI: 1.04-4.6, respectively) when adjusted for additional high-risk features. Patients with MYChigh tumors also tended to have additional high-risk features and to be older at diagnosis. A subgroup of 13 patients had concomitant MYChigh expression and TP53/p53 alterations and a substantially increased risk of progression (HR=16.9, 95% CI: 7.4-38.3) and death (HR=7.8, 95% CI: 4.4-14.1) with an average overall survival of only 0.9 years. In summary, we found that at diagnosis a subset of MCL patients (14%) overexpressed MYC protein, and had a poor prognosis but that MYC rearrangements were rare. Tumors with concurrent MYC overexpression and TP53/p53 alterations pinpointed MCL patients with a dismal prognosis with a median overall survival of less than 3 years. We propose that MYC needs to be assessed beyond the current high-risk factors in MCL in order to identify cases in need of alternative treatment.

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1457590057
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.3324.haematol.2023.283352