Table 3.
Common Somatic Mutations in PDTC Calculated Based on Combined Data from Four NGS Studiesa
| Mutations | % of tumors | Mutations | % of tumors |
|---|---|---|---|
| RAS-RAF-MAPK pathway | TERT promoter mutation | 40 | |
| BRAFV600E | 27 | Tumor suppressors | |
| RAS | 24 | TP53 | 16 |
| NRAS | 17 | ATM | 8 |
| KRAS | 3 | RB1 | 2 |
| HRAS | 4 | CHEK2 | 2 |
| PI3K-AKT-mTOR pathway | MEN1 | 1 | |
| PTEN | 4 | Other mutations | |
| PIK3CA | 3 | EIF1AX | 11 |
| AKT1 | 2 | ABL1 | 4 |
| AKT3 | 1 | GNAS | 3 |
| STAT pathway | HNF1A | 3 | |
| JAK3 | 3 | RECQL4 | 3 |
| RAS + PI3K pathway | IDH1 | 2 | |
| EGFR | 4 | STK11 | 2 |
| PDGFRA | 2 | TSHR | 2 |
| RAS + PI3K + STAT pathway | Histone methyltransferases | 7 | |
| FLT3 | 4 | SWI/SNF complex | 5 |
| MET | 2 | MMR genes | 2 |
| ALK | 1 | RBM10* | 12 |
| Wnt pathway | MED12* | 15 | |
| APC | 4 | ||
| CDH1 | 3 | ||
| CTNNB1 | 1 |
References (46–49).
Novel alterations in fatal PDTC (% of fatal PDTC).
NGS, next-generation sequencing.