Group by Gene: PARP Inhibitors Tyrosine Kinase Inhibitors BCL Inhibitors Chemotherapy Other CD Protein Inhibitors Immune Checkpoint Inhibitors Immunotherapy Serine-Threonine Kinase Inhibitors DNA Threonine-Tyrosine Kinase Inhibitors Hormone Therapy | bevacizumab-tnjn | bevacizumab-maly | VEGF-A inhibitor bevacizumab-awwb | Aybintio (bevacizumab biosimilar) | bevacizumab | bevacizumab-adcd | VEGF-A inhibitor, PARP inhibitor bevacizumab + olaparib | bevacizumab + niraparib | niraparib | PARP inhibitor rucaparib | olaparib | pamiparib | cisplatin + gemcitabine | DNA synthesis inhibitor cisplatin | gemcitabine | anastrozole | Aromatase inhibitor letrozole | exemestane | Topoisomerase II inhibitor doxorubicin hydrochloride | pegylated liposomal doxorubicin | Tubulin polymerization promoter, Bcl2 inhibitor, Tubulin inhibitor carboplatin + micellar paclitaxel | carboplatin + albumin-bound paclitaxel | Topoisomerase I inhibitor topotecan | irinotecan | Alkylating agent melphalan | cyclophosphamide | GnRH agonist leuprolide acetate | Topoisomerase II inhibitor, Tubulin polymerization promoter carboplatin + pegylated liposomal doxorubicin | Thymidylate synthase inhibitor capecitabine | Tubulin polymerization promoter, DNA synthesis inhibitor carboplatin + gemcitabine | Bifunctional alkylating agent, DNA synthesis inhibitor cisplatin + ifosfamide | Bifunctional alkylating agent, Tubulin polymerization promoter carboplatin + ifosfamide | Tubulin polymerization promoter carboplatin | Estrogen receptor antagonist tamoxifen | Tubulin polymerization promoter, Bcl2 inhibitor carboplatin + paclitaxel | paclitaxel | Progesterone receptor agonist megestrol | Multi-tyrosine kinase inhibitor pazopanib | Tubulin polymerization inhibitor vinorelbine tartrate | Bcl2 inhibitor, Tubulin inhibitor albumin-bound paclitaxel | DNA synthesis inhibitor, DNA cross linking agent oxaliplatin | Bifunctional alkylating agent ifosfamide | MEK inhibitor trametinib | Selective estrogen receptor degrader fulvestrant | Topoisomerase II inhibitor, DNA inhibitor etoposide oral | TrkB receptor inhibitor, TrkC kinase inhibitor, TrkA receptor inhibitor larotrectinib | VEGFR inhibitor, DLL4 inhibitor OMP-305B83 | PD1 inhibitor pembrolizumab | PARP1 inhibitor BSI 201 | RET inhibitor selpercatinib | EP | BEP | Chemotherapy IP | VAC | CAPOX | FOLFOX | Bifunctional alkylating agent, Tubulin polymerization promoter, Bcl2 inhibitor paclitaxel + ifosfamide | Microtubule stabilizer, Tubulin polymerization promoter carboplatin + docetaxel | pan-RAF inhibitor, Multi-tyrosine kinase inhibitor sorafenib | VEGF-A inhibitor, Folate receptor 1-targeted antibody-drug conjugate, Microtubule inhibitor bevacizumab + mirvetuximab soravtansine-gynx | Tubulin polymerization promoter, DNA synthesis inhibitor, Bcl2 inhibitor cisplatin + paclitaxel | THF dehydrogenase inhibitor, Thymidylate synthase inhibitor pemetrexed | TrkB receptor inhibitor, TrkC kinase inhibitor, ROS1 inhibitor, TrkA receptor inhibitor, ALK inhibitor, JAK2 inhibitor, TNK2 inhibitor entrectinib | Folate receptor 1-targeted antibody-drug conjugate, Microtubule inhibitor STRO-002 | mirvetuximab soravtansine-gynx | VEGF-A inhibitor, Microtubule inhibitor bevacizumab + ixabepilone |
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No biomarker | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
FOLR1 expression | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
FOLR1 positive | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
HRD + BRCA1 mutation | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
HRD + BRCA2 mutation | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
BRCA2 mutation | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
BRCA1 mutation | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
NTRK3 fusion | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
NTRK1 fusion | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
MSI-H/dMMR | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
HRD | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
TMB-H | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
RAD51C mutation | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
PD-L1 expression | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
NTRK2 fusion | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
RET fusion | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
TUBB3 expression |