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Genetic differences between benign phyllodes tumors and fibroadenomas revealed through targeted next generation sequencing.

Ng CCY,Md Nasir ND,Loke BN,Tay TKY,Thike AA,Rajasegaran V,Liu W,Lee JY,Guan P,Lim AH,Chang KTE,Gudi MA,Madhukumar P,Tan BKT,Tan VKM,Wong CY,Yong WS,Ho GH,Ong KW, ,Yip GWC,Bay BH,Tan P,Teh BT,Tan PH
阅读:39 Modern PathologyVolume 34 Issue 7, July 2021:1320-1332 

Abstract

Breast fibroepithelial lesions are biphasic tumors which comprise the common benign fibroadenomas (FAs) and the rarer phyllodes tumors (PTs). This study analyzed 262 (42%) conventional FAs, 45 (7%) cellular FAs, and 321 (51%) benign PTs contributed by the International Fibroepithelial Consortium, using a previously curated 16 gene panel. Benign PTs were found to possess a higher number of mutations, and higher rates of cancer driver gene alterations than both groups of FAs, in particular MED12, TERT promoter, RARA, FLNA, SETD2, RB1, and EGFR. Cases with MED12 mutations were also more likely to have TERT promoter, RARA, SETD2, and EGFR. There were no significant differences detected between conventional FAs and cellular FAs, except for PIK3CA and MAP3K1. TERT promoter alterations were most optimal in discriminating between FAs and benign PTs. Our study affirms the role of sequencing and key mutations that may assist in refining diagnoses of these lesions.

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