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Genetic characterisation of sarcomatoid carcinomas reveals multiple novel actionable mutations and identifies KRAS mutation as a biomarker of poor prognosis.
- Source :
-
Journal of medical genetics [J Med Genet] 2022 Jan; Vol. 59 (1), pp. 10-17. Date of Electronic Publication: 2020 Oct 28. - Publication Year :
- 2022
-
Abstract
- Background: Sarcomatoid component occurs in various epithelial malignancies and is associated with an aggressive disease course and poor clinical outcome. As it is largely rare, the molecular events underlying sarcomatoid carcinomas (SCs) remain poorly characterised. Here, we performed targeted next-generation sequencing (NGS) on patients with surgically resected SCs comprising distinct tissues of origin.<br />Methods: A total of 71 patients with pathological diagnosis of sarcomatoid carcinomas and underwent surgery were retrospectively enrolled in this study. Overall survival (OS) was defined as the time from surgery to death from any cause. Patients alive or lost to follow-up were censored. Genomic DNA from formalin-fixed paraffin-embedded samples was extracted for NGS and tumour mutation burden (TMB) analysis.<br />Results: In general, SCs occurred more commonly in males, except those of the gallbladder. SCs of the lung and the larynx were associated with a higher proportion of smokers (p=0.0015). Alterations in TP53 , RB1 , TERT and KRAS were highly frequent, with KRAS mutations being a biomarker of poor prognosis (median OS=8 vs 16 months, p=0.03). Multiple alterations in potentially actionable genes, including ROS1 and NTRK1 fusions and ERBB2 amplification, were detected in the extra-pulmonary cohort. A relatively high proportion (30%) of patients with extra-pulmonary SC had high TMB, with a median of 5.39 mutations per Mb. Lastly, copy number variations were common in SCs, and were non-overlapping between the primary and metastatic tumours.<br />Conclusion: Taken together, our results suggest that comprehensive genetic testing may be necessary to inform treatment options and identify prognostic biomarkers.<br />Competing Interests: Competing interests: JCY, DZ, CN and YWS are employees of Nanjing Geneseeq Technology Inc. All other authors have declared no conflict of interests.<br /> (© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.)
- Subjects :
- Aged
Asian People genetics
Biomarkers, Tumor
Carcinoma metabolism
Female
High-Throughput Nucleotide Sequencing
Humans
Male
Middle Aged
Oncogene Proteins genetics
Prognosis
Retinoblastoma Binding Proteins genetics
Retrospective Studies
Sequence Analysis, DNA
Telomerase genetics
Tumor Suppressor Protein p53 genetics
Ubiquitin-Protein Ligases genetics
Carcinoma genetics
Mutation
Proto-Oncogene Proteins p21(ras) genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1468-6244
- Volume :
- 59
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of medical genetics
- Publication Type :
- Academic Journal
- Accession number :
- 33115932
- Full Text :
- https://doi.org/10.1136/jmedgenet-2020-107083