Abstract 967P
Background
HCC is a primary malignant liver disease usually presenting with single or multiple nodules developing from underlying chronic hepatitis or cirrhosis. The Polycomb group (PcG) proteins and DNA methylation systems are epigenetic systems involved in hereditary gene activation inhibition. These epigenetic systems are involved in regulating gene expression and are closely related to the development of HCC. EZH2 is a functional enzymatic component of Polycomb Repressive Complex 2 (PRC2). The inhibition of tumor suppressor genes by EZH2 has been observed, and impeding the activity of EZH2 has been shown to decelerate tumor growth. According to some studies, EZH2 expression is associated with aggressive tumor behavior, a poor prognosis, and a poor response to treatment. The goal was to determine if EZH2 expression levels in HCC are of prognostic significance.
Methods
We picked 103 patients who had pathological diagnoses between 2011-2019. Retrospective screenings were done. EZH2 was checked with immunohistochemistry. Survival and treatment responses were analyzed statistically.
Results
89 (86.4%) patients were male, and 14 (13.6%) were female. The median age of the patients was 68 (min19- max 89). 1% and above was considered positive. Immunohistochemically, EZH2 showed positive staining in 45 (43.7%) patients, and no staining was observed in 58 (56.3%) patients. The patients' median progression-free survival (mPFS) in the positive group was 5 months, while the mPFS of the negative group was 9 months (p=0.012). Based on comprehensive survival analysis, 35 of 45 patients in the positive group had died, and 10 were still alive. In the negative group, 36 patients died, and 22 survived. In the positive group, the median overall survival (mOS) was 8 months; in the negative group, it was 27 months (p=0,007). In our study, EZH2 had prognostic significance for progression-free and overall survival. Furthermore, an increase in EZH2 expression level was associated with a poor prognosis.
Conclusions
We established the prognostic significance of EZH2 for HCC. These findings could lead to new therapeutic strategies (e.g. tazemetostat) for treating and managing HCC. A greater understanding of EZH2's role in HCC requires further research.
Clinical trial identification
Editorial acknowledgement
TRANSLATE with x
English
Legal entity responsible for the study
The authors.
Funding
Cukurova University Scientific Research Project Unit.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
832P - Characterisation of EXS73565: A potent and selective MALT1 inhibitor with low drug-drug interaction risk and potential in lymphoma
Presenter: Major Gooyit
Session: Poster session 18
833P - New targets for adult T cell leukemia/lymphoma (ATLL): A map for ATLL immunotherapy
Presenter: Zahra Rezaei Borojerdi
Session: Poster session 18
834P - Phase II clinical study of VR-CAP regimen for first-line treatment of marginal zone lymphoma
Presenter: Junfeng Chu
Session: Poster session 18
835P - A safe and effective immunochemotherapy with oral sobuzoxane and etoposide for untreated diffuse large B cell lymphoma patients aged 80 and over
Presenter: Kaname Miyashita
Session: Poster session 18
838P - Matching-adjusted indirect comparison (MAIC) of axicabtagene ciloleucel (axi-cel) and epcoritamab (epcor) in relapsed/refractory (R/R) large B cell lymphoma (LBCL) after at least two prior systemic therapies (3L+)
Presenter: Olalekan Oluwole
Session: Poster session 18
840P - Genomic landscape, immune characteristics and prognostic mutation signature of extranodal NK/T cell lymphoma, nasal type in China
Presenter: Yue Chai
Session: Poster session 18
841P - Ki67-revised risk index to risk-stratify patients with extra-nodal natural killer/T cell lymphoma
Presenter: Shuo Li
Session: Poster session 18