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. Author manuscript; available in PMC: 2021 Mar 1.
Published in final edited form as: Gynecol Oncol. 2020 Jan 2;156(3):552–560. doi: 10.1016/j.ygyno.2019.12.015

Table 2.

Potentially targetable events in MOC.

Genetic event Na in MOC (%) Potential therapy
Currently in the clinic for other cancer types 79 (42.9%)
ERBB2 amplification 51 (26.7%) Anti Her2 monoclonal antibody therapy, Anti Her2 Mab conjugate therapies, Anti-Her2 tyrosine kinase inhibitors
BRAF mutation (any) 16 (8.7%) BRAF inhibitors
BRAF mutation (V600E) 9 (4.9%)
 High HRD score (>55) 1 (0.5%) Platinum salts, PARP inhibitors
 Moderate HRD score (42-55) 7 (3.8%)
 ER positivity 14 (10.6%) Anti-estrogens, CDK4/6 inhibition
 Mismatch repair deficiency 1 (0.5%) Immune checkpoint inhibitors
Currently in trials for other cancer types 167 (90.8%)
KRAS, NRAS mutation 118, 3 (65.8%) Broad spectrum RAS/RAF inhibition, MEK inhibition
TP53 missense mutation 90 (48.9%) Mutant p53 reactivators
RNF43 mutation 21 (11.4%) FZD inhibition, PORCN inhibitors
ARID1A mutation 19 (10.3%) Epigenetic modifiers (e.g. BET inhibitors, EZH2 inhibitors), ATR inhibitors
PIK3CA mutation, PTEN inactivating 15,2 (9.2%) PI3-kinase inhibitors, AKT inhibitors
ERBB3 mutation 8 (4.3%) Anti-Her2 tyrosine kinase inhibitors, anti-Her3 Mab conjugate therapies
Not yet targetable
CDKN2A inactivating 82 (44.6%)
TP53 truncating/ESS mutation 30 (16.3%)
a

Mutation data denominator = 184; copy number denominator = 191.