- January 30, 2026
- Hussein Abbas, et al., MD Anderson
Topic/Product:
Inflammation Panel 250
Disease Area:
Differentiation Syndrome associated with AML therapy
Sample Type:
Plasma, Serum
Abstract
High-throughput proteomic profiling provides a comprehensive analysis of systemic cancer effects and tumor microenvironment interactions. Characterizing soluble proteins driving inflammation in acute myeloid leukemia (AML) offers insight into inflammatory diseases like differentiation syndrome related to AML therapies like menin inhibitors. We present our application of nucleic acid-linked immuno-sandwich assay, a novel technology leveraging next-generation sequencing for high-throughput, ultrasensitive characterization of secreted inflammatory proteins in plasma or serum. Here, we report its use to identify dynamic soluble protein changes during treatment and at the time of suspected differentiation syndrome in pediatric AML patients treated with the menin inhibitor revumenib (NCT04065399 and NCT05360160).
Authors & Affiliations
Miriam B. Garcia¹, Bofei Wang², Irtiza Sheikh¹, Georgina El Hajjar², David McCall¹, Cesar Nunez¹, Amber Gibson¹, Philip L. Lorenzi³, Ghayas C. Issa², Branko Cuglievan¹, and Hussein A. Abbas²⁴
¹ Department of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
² Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
³ Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
⁴ Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
