Tamoxifen and aromatase inhibitors |
Estrogen receptor expression |
Fujii et al., 2017
|
HER2-directed therapies |
HER2 amplification and overexpression |
Sartore-Bianchi et al., 2016
|
ALK/ROS1 inhibitors |
ALK and ROS1 rearrangements |
Soda et al., 2007; Kwak et al., 2009; Shaw et al., 2014
|
EGFR-directed therapies (sensitivity) |
EGFR mutations |
Lynch et al., 2004; Paez et al., 2004; Pao et al., 2004
|
EGFR-directed therapies (resistance) |
KRAS/NRAS/BRAF mutations |
Siddiqui and Piperdi, 2010; Waring et al., 2016; van Brummelen et al., 2017
|
PARP inhibitors |
BRCA1/2 mutations, BRCAness |
Iyevleva and Imyanitov, 2016; Lord and Ashworth, 2016
|
Platinum compounds, mitomycin C |
BRCA1/2 mutations, BRCAness |
Iyevleva and Imyanitov, 2016; Lord and Ashworth, 2016
|
PD1-directed therapies |
High PD-L1 expression |
Kumar et al., 2017
|
Immune checkpoint inhibitors |
Tumor mutation burden |
Rizvi et al., 2015
|
BRAF inhibitors |
BRAF mutations |
Ugurel et al., 2017; Cheng et al., 2018
|
mTOR inhibitors |
TSC1/2 mutations, MTOR mutations |
Kwiatkowski et al., 2016
|
MET inhibitors |
MET exon 14 skipping |
Pilotto et al., 2017
|