Group by Gene: Include preclinical: Chemotherapy Other DNA CD Protein Inhibitors Immune Checkpoint Inhibitors Immunotherapy Tyrosine Kinase Inhibitors Chemokine Epigenetics Threonine-Tyrosine Kinase Inhibitors IGF Cyclin Dependent Kinase Inhibitors Serine-Threonine Kinase Inhibitors Proteasome Inhibitors FGF | Topoisomerase I inhibitor topotecan | irinotecan | Topoisomerase II inhibitor, RNA synthesis inhibitor dactinomycin | Alkylating agent, DNA inhibitor trabectedin | THF dehydrogenase inhibitor, Dihydrofolic acid reductase inhibitor methotrexate | Mitosis inhibitor vinorelbine | Topoisomerase II inhibitor doxorubicin hydrochloride | Alkylating agent, Tubulin polymerization inhibitor cyclophosphamide + vinorelbine tartrate | Bifunctional alkylating agent, Topoisomerase II inhibitor doxorubicin hydrochloride + ifosfamide | Bifunctional alkylating agent, Topoisomerase II inhibitor, Tubulin polymerization inhibitor doxorubicin hydrochloride + ifosfamide + vincristine | PD1 inhibitor nivolumab | T-lymphocyte cell therapy T-lymphocyte cell therapy | Chemotherapy VAC | IE | Topoisomerase II inhibitor, Tubulin polymerization promoter, DNA inhibitor carboplatin + etoposide oral | Alkylating agent, Topoisomerase I inhibitor cyclophosphamide + topotecan | Topoisomerase II inhibitor, Tubulin polymerization inhibitor, RNA synthesis inhibitor vincristine + dactinomycin | Tubulin polymerization inhibitor, DNA synthesis inhibitor, Topoisomerase I inhibitor temozolomide + irinotecan + vincristine | Bifunctional alkylating agent, Topoisomerase II inhibitor, Alkylating agent, Tubulin polymerization inhibitor doxorubicin hydrochloride + cyclophosphamide + ifosfamide + vincristine | Topoisomerase II inhibitor, Alkylating agent, Tubulin polymerization inhibitor doxorubicin hydrochloride + cyclophosphamide + etoposide IV + vincristine | Tubulin polymerization inhibitor, Topoisomerase I inhibitor irinotecan + vincristine | MEK inhibitor, IGF-1R inhibitor trametinib + AMG 479 | XPO1 inhibitor, CDK9 inhibitor, P-TEFb inhibitor selinexor + VIP152 | Proteasome inhibitor, CDK9 inhibitor, P-TEFb inhibitor bortezomib + VIP152 | carfilzomib + VIP152 | CDK9 inhibitor, P-TEFb inhibitor VIP152 | FGFR4 inhibitor ABSK012 | Multi-tyrosine kinase inhibitor anlotinib | pazopanib | ALK inhibitor crizotinib | CXCL12 inhibitor, Farnesyl transferase inhibitor tipifarnib | LSD1 inhibitor SP2577 | HDAC inhibitor, HDAC1 inhibitor, HDAC2 inhibitor, HDAC3 inhibitor entinostat | CXCL12 inhibitor, Farnesyl transferase inhibitor, MEK inhibitor trametinib + tipifarnib |
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No biomarker | ||||||||||||||||||||||||||||||||||
PD-L1 expression | ||||||||||||||||||||||||||||||||||
EWSR1-TFCP2 fusion | ||||||||||||||||||||||||||||||||||
HRAS mutation | ||||||||||||||||||||||||||||||||||
KDM1A overexpression | ||||||||||||||||||||||||||||||||||
PAX3-FOXO1 fusion | ||||||||||||||||||||||||||||||||||
HER-2 expression | ||||||||||||||||||||||||||||||||||
RAS mutation | ||||||||||||||||||||||||||||||||||
MYCN amplification | ||||||||||||||||||||||||||||||||||
FGFR4 V550L | ||||||||||||||||||||||||||||||||||
BRAF-MAD1L1 fusion |