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. 2020 May 18;105(7):e2346–e2357. doi: 10.1210/clinem/dgaa246

Table 1.

Genomic alterations deemed to be potentially productively therapeutically targetable

Mutation/ Alteration Corresponding targeted agents Histology: DTC/PDTC, 25 ATC, 19 MTC, 8 No. of alterations
AURKB Pazopanib, AMG900 ATC (vus) 1
ALK Crozotinib Ceritinib Alectanib ATC (vus) 1
BRAFV600E Vemurafenib dabrafenib PTC ATC 10 (40%) 6 (32%) –
BRCA1-2 Olaparib Rusaparib Nuraparib PTC (vus) PDTC (vus) HCC (vus) 1 2 1
ERBB2-3 Trastuzumab Pertuzumab ATC (vus) ATC/PTC (vus) 2 2
FGF/R Pazopabib Ciritinib PTC (vus) PDTC (vus) ATC (vus) 2 1 3
JAK Roxolitinib Tofacitinib PTC (vus) ATC (vus) 4 1
MSH2/6 (Confers increased sensitivity to anti–PD-L1/PD-1 therapy) Pembrolizumab Nivolumab PTC PDTC ATC ATC (vus) ATC/PTC (vus) 1 1 1 1 1
MTOR Everoliums Temsirolimus PTC ATC/PTC (vus) 2 1
PDGFRA/B Pazopanib Lenvatinib ATC/PDTC 1
PI3K Alpelisib ATC/PTC 2
RET Vandetanib Cabozantinib, LOXO-292 BLU-667 HCC (vus) ATC (vus) ATC/PTC (vus) MTC 1 1 1 3
ROS Crozotinib Ciritinib Alectanib PDTC (vus) 1
TOP2A Etoposide Doxorubicin ATC/PTC (vus) 1

Abbreviations: ATC, anaplastic thyroid cancer; DTC, differentiated thyroid cancer; HCC, Hürthle cell cancer; MTC, medullary thyroid cancer; PDTC, progression to poorly differentiated thyroid cancer; PTC, papillary thyroid cancer; vus, variant of uncertain significance.