2026/03/26 by Burak Uzunparmak, Fei Su, A. Johnson +22 · 1 voice
Biochemistry, Genetics and Molecular Biology · Medicine · #Cancer Genomics and Diagnostics #Lung Cancer Research Studies #Lung Cancer Treatments and Mutations
paper · doi:10.1158/2159-8290.cd-25-1304
openalex publication_date 2026/03/26 · openalex created_date 2026/03/27 · openalex updated_date 2026/06/17
Abstract The added value of comprehensive genomic and transcriptomic profiling (CGTP) with whole-exome sequencing (WES) and whole-transcriptome sequencing (WTS) as compared with conventional targeted panel-based sequencing is not well-characterized for patients with cancer. We thus sought to determine the potential clinical utility of CGTP in a prospective clinical study in patients with advanced or metastatic solid tumors. We performed WES and WTS for patients who had prior targeted panel sequencing and had no DNA alterations with approved biomarker-matched therapies. We analyzed CGTP data of 99 patients with advanced cancers across 19 solid tumor types and assessed the presence of actionable DNA alterations and RNA expressions linked to approved or investigational agents. CGTP identified actionable genomic and transcriptomic alterations in 69.7% and 100% of cases, respectively. In this pilot study in which CGTP was incorporated into routine care, 19.2% of patients received biomarker-matched therapy. Significance: This study demonstrates the feasibility and utility of extensive genomic and transcriptomic profiling to match patients with advanced cancer to molecularly informed treatments. Transcriptomic actionability analysis identifies actionable RNA expressions for patients beyond those with actionable DNA alterations, highlighting the potential of transcriptional profiling to enhance therapeutic opportunities in precision oncology.