Key result
Blood-based next-generation sequencing detected at least one somatic alteration in 80% of patients with adrenocortical carcinoma, with 47% having actionable mutations.
Why the study?
Adrenocortical carcinoma is a rare, heterogeneous malignancy with poor prognosis, prompting evaluation of the feasibility of circulating cell-free tumor DNA next-generation sequencing to characterize genomic alterations and identify actionable mutations.
Does blood-based next-generation sequencing of ctDNA identify clinically actionable mutations in patients with adrenocortical carcinoma?
Observational (n=120)
Does blood-based next-generation sequencing of ctDNA identify clinically actionable mutations in patients with adrenocortical carcinoma?
Answers are grounded in this paper and cite their sources.
Blood-based next-generation sequencing of ctDNA is feasible in over 80% of patients with advanced adrenocortical carcinoma and identifies actionable mutations in nearly half of them.
BACKGROUND: Adrenocortical carcinoma (ACC) is a rare and heterogeneous malignancy with poor prognosis. We aimed to evaluate the feasibility of next-generation sequencing (NGS) testing of circulating cell-free tumor DNA (ctDNA) in patients with ACC, to characterize the genomic landscape of alterations, and to identify potential clinically actionable mutations. METHODS: Retrospective analysis of genomic data from 120 patients with ACC who had ctDNA testing between 12/2016 and 10/2021 using Guardant360 (Guardant Health, CA) was performed. ctDNA NGS analysis interrogated single nucleotide variants, fusions, indels, and copy number amplifications of up to 83 genes. The frequency of genomic alterations, landscape of co-occurring mutations, and pathogenic/likely pathogenic alterations with potential targeted therapies was identified. The prevalence of alterations identified in ctDNA was compared to those detected in tissue using a publicly available database (cBioPortal). RESULTS: The median age of this cohort was 53 years (range 21-81), and 56% of patients were female. Ninety-six patients (80%) had ≥1 somatic alteration detected. TP53 (52%), EGFR (23%), CTNNB1 (18%), MET (18%), and ATM (14%) were found to be the most frequently altered genes in ACC samples. Pathogenic and/or likely pathogenic mutations in therapeutically relevant genes were observed in 56 patients (47%) and included EGFR, BRAF, MET, CDKN2A, CDK4/6, and ATM. The most frequent co-occurring mutations were EGFR + MET (9%), MET + CDK4 (7%), EGFR + CDK4 (7%), and BRAF + MET (7%). The frequencies of mutations detected in ctDNA were similar to those detected in tissue. CONCLUSIONS: Utilizing blood-based NGS to characterize genomic alterations in advanced ACC is feasible in over 80% of patients. Almost half of the patients had actionable mutations with approved therapies in other cancers. This approach might inform the development of personalized treatment options or identify clinical trials available for this aggressive malignancy.
No takes yet. Share an insight, caveat, or question.
Nazha et al. (2022) conducted an observational in Adrenocortical carcinoma (n=120). Blood-based next-generation sequencing (ctDNA testing) vs. Tissue testing (cBioPortal database) was evaluated on Detection of ≥1 somatic alteration. Blood-based next-generation sequencing detected at least one somatic alteration in 80% of patients with adrenocortical carcinoma, with 47% having actionable mutations.
Synapse has enriched 10 related papers. Consider them for comparative context: