Group by Gene: RAS Serine-Threonine Kinase Inhibitors Threonine-Tyrosine Kinase Inhibitors Tyrosine Kinase Inhibitors Chemotherapy Other CD Protein Inhibitors Immune Checkpoint Inhibitors Immunotherapy DNA BCL Inhibitors Cyclin Dependent Kinase Inhibitors MDM2/MDMX EGFR | PD-L1 inhibitor durvalumab | VEGF-A inhibitor bevacizumab | TrkB receptor inhibitor, TrkC kinase inhibitor, TrkA receptor inhibitor larotrectinib | KRAS G12C inhibitor sotorasib | adagrasib | MEK inhibitor, BRAF inhibitor trametinib + dabrafenib | mTOR inhibitor everolimus | MDM2-p53 antagonist BI 907828 | DNA synthesis inhibitor, Bcl2 inhibitor, Tubulin inhibitor gemcitabine + albumin-bound paclitaxel | cisplatin + gemcitabine + albumin-bound paclitaxel | RET inhibitor selpercatinib | Chemotherapy FOLFIRINOX | Folate analog, Thymidylate synthase inhibitor 5-fluorouracil + leucovorin calcium | MEK inhibitor MEK inhibitor | TrkB receptor inhibitor, TrkC kinase inhibitor, ROS1 inhibitor, TrkA receptor inhibitor, ALK inhibitor, JAK2 inhibitor, TNK2 inhibitor entrectinib | HER2 inhibitor, HER4 inhibitor, EGFR inhibitor afatinib | HER2 inhibitor, CDK4 inhibitor, CDK6 inhibitor, HER2 dimerization inhibitor palbociclib + pertuzumab + abemaciclib + ribociclib + trastuzumab / hyaluronidase-oysk | cRAF inhibitor, MEK inhibitor, BRAF inhibitor binimetinib + encorafenib | DNA synthesis inhibitor gemcitabine |
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No biomarker | |||||||||||||||||||
KRAS G12C | |||||||||||||||||||
NTRK1 fusion | |||||||||||||||||||
BRAF V600E | |||||||||||||||||||
BRAF D594G | |||||||||||||||||||
NTRK3 fusion | |||||||||||||||||||
RET fusion | |||||||||||||||||||
HER-2 G660D + HER-2 S310F | |||||||||||||||||||
KRT7 expression | |||||||||||||||||||
KRT7 expression + MUC1 expression | |||||||||||||||||||
HER-2 mutation + CDK6 mutation | |||||||||||||||||||
PIK3CA mutation | |||||||||||||||||||
NTRK2 fusion | |||||||||||||||||||
NRAS mutation + BRAF mutation | |||||||||||||||||||
MDM2 amplification | |||||||||||||||||||
MUC2 negative |