Concordance analysis of DNA and RNA profiling: The MD Anderson IMPACT2 study in precision oncology
Summary
DNA profiling is an established method for cancer treatment selection, while RNA profiling remains investigational. We explored associations between DNA and RNA alterations and between the number of genes with altered expression and overall survival (OS) using patient data from IMPACT2 (NCT02152254), a randomized study evaluating molecular profiling for guiding cancer therapy across tumor types. Molecular profiling, including DNA next-generation sequencing, was performed on all 829 patient
Content
# Concordance analysis of DNA and RNA profiling: The MD Anderson IMPACT2 study in precision oncology
*Published: 2026 Feb 24*
DNA profiling is an established method for cancer treatment selection, while RNA
profiling remains investigational. We explored associations between DNA and RNA
alterations and between the number of genes with altered expression and overall
survival (OS) using patient data from IMPACT2 (NCT02152254), a randomized study
evaluating molecular profiling for guiding cancer therapy across tumor types.
Molecular profiling, including DNA next-generation sequencing, was performed on
all 829 patients in the IMPACT2 study. RNA profiling was performed by Tempus for
253 of 829 patients. We evaluated the concordance between DNA and RNA profiling,
analyzed OS in 217 treated patients with RNA profiling, and assessed PD-L1
status and number of genes with altered expression. Fifty patients exhibited 58
concordant events, i.e., genomic and expression alteration(s) in the same gene,
including 38 copy number events, and 41 patients had statistically significant
concordance. We identified 123 gene pairs with significant associations between
genomic and expression alterations (p < 0.05), including TP53 alterations with
VEGFA overexpression. The median OS for patients with 0-2, 3-5, and ≥6 genes
with altered expression was 9.8, 11.9, and 6.7 months, respectively (p = 0.03).
These results underscore RNA profiling's potential actionability, and altered
expression in ≥6 genes was associated with shorter OS. Significant concordance
of TP53 alterations with VEGFA overexpression may partially explain tumor
response to bevacizumab in TP53-mutant patients.
DOI: 10.1038/s41392-026-02580-0