Unknown

Dataset Information

0

Molecular profiling of soft-tissue sarcomas with FoundationOne® Heme identifies potential targets for sarcoma therapy: a single-centre experience.


ABSTRACT:

Background

Molecular diagnosis has become an established tool in the characterisation of adult soft-tissue sarcomas (STS). FoundationOne® Heme analyses somatic gene alterations in sarcomas via DNA and RNA-hotspot sequencing of tumour-associated genes.

Methods

We evaluated FoundationOne® Heme testing in 81 localised STS including 35 translocation-associated and 46 complex-karyotyped cases from a single institution.

Results

Although FoundationOne® Heme achieved broad patient coverage and identified at least five genetic alterations in each sample, the sensitivity for fusion detection was rather low, at 42.4%. Nevertheless, potential targets for STS treatment were detected using the FoundationOne® Heme assay: complex-karyotyped sarcomas frequently displayed copy-number alterations of common tumour-suppressor genes, particularly deletions in TP53, NF1, ATRX, and CDKN2A. A subset of myxofibrosarcomas (MFS) was amplified for HGF (n = 3) and MET (n = 1). PIK3CA was mutated in 7/15 cases of myxoid liposarcoma (MLS; 46.7%). Epigenetic regulators (e.g. MLL2 and MLL3) were frequently mutated.

Conclusions

In summary, FoundationOne® Heme detected a broad range of genetic alterations and potential therapeutic targets in STS (e.g. HGF/MET in a subset of MFS, or PIK3CA in MLS). The assay's sensitivity for fusion detection was low in our sample and needs to be re-evaluated in a larger cohort.

SUBMITTER: Scheipl S 

PROVIDER: S-EPMC8317253 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC6337155 | biostudies-literature
| S-EPMC3353406 | biostudies-other
| S-EPMC7757586 | biostudies-literature
| S-EPMC7050044 | biostudies-literature
| S-EPMC6311917 | biostudies-literature
| S-EPMC8303572 | biostudies-literature
| S-EPMC4344612 | biostudies-literature
| S-EPMC4219423 | biostudies-literature
| S-EPMC2911503 | biostudies-literature
| S-EPMC7292898 | biostudies-literature