Table 3.
Case no. | Histology | KRAS mutation | Peak height on SE |
KRAS FISH
|
||
---|---|---|---|---|---|---|
KRAS/CEP12 | % Of cells with hyperploidy | % Of cells with monosomy | ||||
1 | Undiff. | p.G12D | MA =WT | 1.1 | 41.2% | N |
PDAa | p.G12D | MA<WT | 1.23 | N | N | |
2 | Undiff. | p.G12D | MA =WT | 2.02 | N | 46.7% |
PDA | p.G12D | MA =WT | 2.43 | N | 68.3% | |
3 | Undiff. | p.G12V | MA =WT | 2.38 | N | N |
PDA | n.t. | n.t. | 3.19 | N | N | |
4 | Undiff. | p.G12D | MA>WT | 2.51 | N | N |
PDA | n.t. | n.t. | 1.29 | 50% | N | |
5 | Undiff. | p.G12V | MA>WT | 4.36 | 64.5% | N |
PDA | n.t. | n.t. | 1.24 | N | 47.6% | |
6 | Undiff. | p.G12V | MA =WT | 9.75 | N | N |
PDAb | p.G12V | MA<WT | 1.28 | N | N | |
7 | Undiff. | p.G12D | MA<WT | 1.02 | N | N |
PDAa | p.G12D | MA<WT | 1.03 | N | N | |
8 | Undiff. | p.G12D | MA<WT | 3.16 | 62.9% | N |
PDA | p.G12D | MA<WT | 1.75 | 88.5% | N | |
9 | Undiff. | p.G12D | MA<WT | 1.1 | 53.8% | N |
PDA | p.G12D | MA<WT | 1.08 | 11.5% | N | |
10 | Undiff. | p.G12D | MA>WT | 1.6 | 40% | N |
PDAb | n.t. | n.t. | 1.19 | 23.3% | N | |
11 | Undiff. | p.G12R | MA<WT | 1.16 | 46.3% | N |
PDA | n.t. | n.t. | 1.1 | 56.3% | N |
Abbreviations: FISH, fluorescence in situ hybridization; MA, mutant allele; N, normal (<40% of cells with hyperploidy or monosomy); n.t., not tested; PDA, well-differentiated component; SE, sequencing electropherogram; Undiff., undifferentiated component; WT, wild-type allele. The proportion (and size) of the PDA component ranged from 1% (0.3 cm) to 40% (3.6 cm).
The PDA component arose from a mucinous cystadenocarcinoma.
The microscopic focus of PDA arose from an intraductal papillary mucinous neoplasm.