Group by Gene: Include preclinical: Tyrosine Kinase Inhibitors FGF Chemotherapy BCL Inhibitors CD Protein Inhibitors Immune Checkpoint Inhibitors Immunotherapy DNA Serine-Threonine Kinase Inhibitors EGFR | Bifunctional alkylating agent ifosfamide | Topoisomerase II inhibitor, DNA inhibitor etoposide oral | Tubulin polymerization promoter carboplatin | DNA synthesis inhibitor gemcitabine | mTOR inhibitor everolimus | Topoisomerase II inhibitor etoposide IV | PD1 inhibitor PD1 inhibitor | pembrolizumab | Multi-tyrosine kinase inhibitor anlotinib | PD-L1 inhibitor, CTLA4 inhibitor KN046 | EGFR inhibitor icotinib | LV5FU2 | ADOC | EP | Chemotherapy CAP | CaT | GEM-CAP | VIP | CAP | VEGFR inhibitor, PDGFR inhibitor, c-KIT inhibitor sunitinib | FGFR inhibitor, VEGFR inhibitor, RET inhibitor, c-KIT inhibitor, PDGFR α antagonist lenvatinib | Tubulin polymerization promoter, Bcl2 inhibitor paclitaxel | THF dehydrogenase inhibitor, Thymidylate synthase inhibitor pemetrexed | DNA synthesis inhibitor, Thymidylate synthase inhibitor gemcitabine + capecitabine | HER2 inhibitor, HER4 inhibitor, EGFR inhibitor pyrotinib | pan-RAF inhibitor, Multi-tyrosine kinase inhibitor sorafenib | PDGFR antagonist, mutant c-KIT inhibitor, CSF-1R inhibitor avapritinib | Mesothelin-targeted antibody-drug conjugate, Microtubule inhibitor BAY 94-9343 |
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No biomarker | ||||||||||||||||||||||||||||
KIT mutation | ||||||||||||||||||||||||||||
KIT D820Y | ||||||||||||||||||||||||||||
KIT exon 17 mutation | ||||||||||||||||||||||||||||
EGFR exon 19 deletion | ||||||||||||||||||||||||||||
HER-2 mutation | ||||||||||||||||||||||||||||
PD-L1 overexpression | ||||||||||||||||||||||||||||
PD-L1 expression | ||||||||||||||||||||||||||||
EGFR exon 20 insertion | ||||||||||||||||||||||||||||
HER-2 positive | ||||||||||||||||||||||||||||
SP140 overexpression | ||||||||||||||||||||||||||||
MSLN expression | ||||||||||||||||||||||||||||
EIF4EBP1 expression | ||||||||||||||||||||||||||||
IGF1R expression |