Loading...

1,267 posters, 47 videos, 13 topics, 4 sessions, 853 authors

ePostersLive by SciGen Technologies S.A. All rights reserved.

SOHO 2026 Annual Meeting

September 9 - 12, 2026 | George R. Brown Convention Center, Houston, Texas

SOHO 2026 Annual Meeting banner

AML - 468

DNMT3A Co-Mutation and Immune Exclusion Signatures Define Outcomes in AML With IDH2 Mutations

Poster Presenter

Feng-Ming Tien

Part of Topic

Acute Myeloid Leukemia (AML)

Title: DNMT3A Co-mutation and Immune Exclusion Signatures Define Outcomes in AML with IDH2 Mutations

Background

Isocitrate dehydrogenase 2 (IDH2)–mutated acute myeloid leukemia (AML) exhibits distinct co-mutation patterns as well as metabolic and epigenetic features. Although mutant IDH–derived oncometabolites may impair antitumor immunity, the transcriptomic basis of immune dysfunction and its prognostic relevance in IDH2-mutated (IDH2mut) AML remain incompletely understood.


Objective/Aim

We integrated genomic and transcriptomic profiling to dissect the heterogeneity of IDH2mut AML.

 

Methods

We analyzed 1,039 de novo non-M3 AML patients treated with standard chemotherapy, with targeted mutational profiling and bulk RNA-seq analysis.  Single-cell RNA sequencing (scRNA-seq) (GSE116256) were used to delineate the cell-type specific dysregulations.

 

Results

IDH2 mutations were identified in 11.9% of patients (R140 7.9%, R172 3.0%). Concurrent DNMT3A mutations were associated with worse OS (P=0.007) and EFS (P=0.038) in those with IDH2 R140 but not those with R172 mutations, which were validated in AMLSG cohort.

Compared to IDH2wt AML, IDH2mut AML displayed significant negative enrichment of interferon-α (IFN-α) (NES -1.76, FDR 2.25E-3), IFN-γ signaling (NES -2.07, FDR 2.65E-8), and allograft rejection signatures (NES -2.31, FDR 2.50E-9), consistent with an immune exclusion phenotype. IDH2mut patients with short EFS (<2 years) showed stronger immune exclusion, with CXCL10, KLF1, and CTSL identified as key DEGs that also stratified OS in BEAT-AML cohort. In scRNA-seq analyses, a total of 10722 cells derived from 9 IDH2wt and 2 IDH2mut patients were analyzed. IFN-α pathway module scores were higher in monocytes, and T cells than progenitor cells. IDH2mut AML exhibited reduced IFN-α module scores specifically within progenitor cells.

 

Conclusions 

In conclusion, DNMT3A co-mutation confers adverse prognosis in IDH2 R140 AML. IDH2 mutations are associated with immune exclusion, particularly in progenitor cells, highlighting the relevance of host immunity in shaping prognosis.

soho2026 banner
Copyright © 2015-2026, ePostersLive® SciGen is a registered trademark of SciGen Technologies S.A. Patent pending.

This website and third-party tools we use rely on cookies for the best user experience. By selecting "I agree", you agree to cookie usage as described in our Privacy Policy.