Table 2.
Tumor ID | TNM | Diagnosis | Treatment prior to tissue collection | Current status | Platform used to detect mutations | BRAF | TP53 | Other mutations | |
---|---|---|---|---|---|---|---|---|---|
1 | P178 | T4bN1bM0 | ATC | None | Deceased | IHC | WT | Yes | None |
2 | P184 | T4bN1bM1 | ATC | None | Deceased | 50-Gene somatic mutation analysis | WT | WT | None |
3 | P215 | T4bN1bM1 | ATC | None | Deceased | IHC and solid tumor genomics assay | WT | R248W | DNMT3A |
4 | P220LN | T4aN1aM1 | ATC with extensive squamous differentiation, LN | Dabrafenib, trametinib | Deceased | IHC and solid tumor genomics assay | V600E | WT | PIK3CA |
5 | P221 | T3NxM0 | ATC arising from a follicular neoplasm | None | Deceased | IHC | WT | WT | None |
6 | P225 | T4aN1bM0 | PTC with anaplastic (undifferentiated) component (~ 10%) | None | Alive | IHC and solid tumor genomics assay | WT | R280K | CDH1 CDKN2A NF1 PIK3CA |
7 | P239 | T4N1bM0 | ATC and PTC | Abraxane, dabrafenib, trametinib | Deceased | IHC and solid tumor genomics assay | V600E | Q331a | None |
8 | P244 | T4aN1bM0 | ATC, squamous type | None | Alive | IHC and solid tumor genomics assay | WT | E56a | TERT RB1 |
9 | P245 | T4aN1bM0 | ATC (40%) with PDTC | None | Deceased | Solid tumor genomics assay | WT | WT | None |
10 | P258 | T4bN1bM0 | ATC | Dabrafenib, trametinib | Deceased | IHC and solid tumor genomics assay | V600E | WT | NF2 TERT |
11 | P264 | T4bN1bM1 | ATC | Radiation | Deceased | IHC and solid tumor genomics assay | D594N | WT | NRAS TERT |
12 | P265 | T4bN1bM1 | ATC | Lenvatinib, dabrafenib, trametinib | Alive | IHC and solid tumor genomics assay | V600E | WT | PIK3CA TERT |
13 | P267 | T4aN0M0 | ATC | None | Alive | Solid tumor genomics assay | WT | R273C | ATM NF1 NOTCH3 RET |
Abbreviations: ATC, anaplastic thyroid cancer; ID, identification; IHC, immunohistochemistry; LN, lymph node; PDTC, poorly differentiated thyroid cancer; TERT, TERT promoter; WT, wild-type.
a Nonsense mutation.