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MYC amplification in angiosarcoma depends on etiological/clinical subgroups – Diagnostic and prognostic value

A.G. Hogeboom-Gimeno, Stefan G. van Ravensteijn, Ingrid M.E. Desar, Melissa H.S. Hillebrandt-Roeffen, Patricia H. J. van Cleef, J.J. Bonenkamp, Uta Flucke, Yvonne M.H. Versleijen‐Jonkers

2022Annals of Diagnostic Pathology21 citationsDOIOpen Access PDF

Abstract

Angiosarcomas (AS) are rare and heterogeneous malignant vascular tumors with a dismal prognosis. We undertook a retrospective study of AS cases with the intent of elucidating the prevalence of MYC amplification amongst different etiological/clinical subgroups and identifying MYC's potential as a prognostic biomarker. Retrospective collection of data and tumor samples from 110 patients diagnosed with AS in the Netherlands was conducted. Histopathological review and investigation of MYC gene amplification and MYC protein overexpression (using fluorescent in situ hybridization and immunohistochemistry, respectively) was performed. MYC amplification was identified in 50.9 % of cases and predominantly present in secondary AS (sAS) (especially radiotherapy-associated and Stewart-Treves AS, both 92.9 %). Within the primary AS (pAS) subgroup, skin non-UV-associated AS (69.2 %) and primary breast AS (29.4 %) demonstrated MYC amplification. MYC protein overexpression was observed in 47.7 % of all tumors with an overall sensitivity and specificity of 75 % and 81 % respectively. There was no significant difference in median overall survival (OS) between patients with MYC and non-MYC amplified AS. Patients with AS displaying MYC protein overexpression had significantly shorter OS than those without (p = 0.028). Although MYC amplification is characteristic for secondary radiotherapy-associated and Stewart-Treves AS, it is not exclusive to these groups and can also be found in a subset of pAS. Overall concordance of FISH and IHC is rather poor. Only primary breast AS showed 100 % concordance. Therefore MYC expression as surrogate marker should be used with caution. The role of MYC/MYC as a prognostic indicator is undefined, however resulting tailored treatment options could be considered.

Topics & Concepts

ConcordanceImmunohistochemistryGene duplicationMedicineEtiologyRetrospective cohort studyBiomarkerPathologyAngiosarcomaIn situ hybridizationFluorescence in situ hybridizationRadiation therapyCancer researchOncologyInternal medicineBiologyGene expressionGeneBiochemistryChromosomeVascular Tumors and AngiosarcomasCardiac tumors and thrombiSarcoma Diagnosis and Treatment
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