Group by Gene: Include preclinical: Immunotherapy Chemotherapy Other Tyrosine Kinase Inhibitors Epigenetics DNA Serine-Threonine Kinase Inhibitors Kinase Inhibitors EGFR IGF Threonine-Tyrosine Kinase Inhibitors PARP Inhibitors Immune Checkpoint Inhibitors BCL Inhibitors Cyclin Dependent Kinase Inhibitors FGF | naxitamab | GD2 ganglioside inhibitor dinutuximab beta | dinutuximab | Alkylating agent melphalan | cyclophosphamide | Topoisomerase II inhibitor doxorubicin hydrochloride | Ornithine decarboxylase inhibitor eflornithine | ALK inhibitor crizotinib | alectinib | WEE1 inhibitor AZD1775 | ROS1 inhibitor, ALK inhibitor lorlatinib | Bcr-abl tyrosine kinase inhibitor, DNA synthesis inhibitor, mTOR inhibitor, Src kinase inhibitor, c-KIT inhibitor, PDGFR β antagonist, EphA2 receptor antagonist dasatinib + temozolomide + sirolimus | ROS1 inhibitor, PTPN11 inhibitor, ALK inhibitor lorlatinib + TNO155 | DNA synthesis inhibitor cisplatin | ATR inhibitor AZD6738 | LRRK2 inhibitor, ALK inhibitor TAE-684 | HDAC inhibitor, EZH2 inhibitor panobinostat + GSK2816126 | BRD3 inhibitor, BRD4 inhibitor, BRD2 inhibitor OTX015 | BET inhibitor, HDAC inhibitor JQ-1 + panobinostat | ALK inhibitor, EGFR inhibitor brigatinib | ALK inhibitor, IGF-1R inhibitor AZD3463 | MEK inhibitor binimetinib | ROS1 inhibitor, Trk inhibitor, ALK inhibitor, Multi-tyrosine kinase inhibitor repotrectinib | PTPN11 inhibitor, ALK inhibitor crizotinib + TNO155 | ceritinib + TNO155 | ERK2 inhibitor, ERK1 inhibitor ASN007 | Chk1 inhibitor, PARP inhibitor olaparib + MK-8776 | Aurora kinase A inhibitor, Bcl2 inhibitor venetoclax + LY3295668 | CDK9 inhibitor KB-0742 | CDK9 inhibitor, P-TEFb inhibitor VIP152 | FGFR2 inhibitor, FGFR inhibitor, FGFR1 inhibitor, FGFR3 inhibitor, ROS1 inhibitor, ALK inhibitor, FGFR4 inhibitor lorlatinib + erdafitinib | ROS1 inhibitor, ALK inhibitor, Multi-tyrosine kinase inhibitor ponatinib + lorlatinib | DLL3-targeted antibody-drug conjugate, DNA replication inhibitor rovalpituzumab tesirine | DNA replication inhibitor, DLK1-targeted antibody-drug conjugate ADCT-701 | B7-H3-targeted antibody-drug conjugate, DNA replication inhibitor MGC018 | CAR-T immunotherapy CAR-T immunotherapy | B7-H3-targeted antibody-drug conjugate B7-H3-targeted antibody-drug conjugate | DHODH inhibitor DHODH inhibitor |
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No biomarker | ||||||||||||||||||||||||||||||||||||||
ALK positive | ||||||||||||||||||||||||||||||||||||||
ALK mutation | ||||||||||||||||||||||||||||||||||||||
ALK R1275Q | ||||||||||||||||||||||||||||||||||||||
ALK D1091N | ||||||||||||||||||||||||||||||||||||||
ALK F1174L | ||||||||||||||||||||||||||||||||||||||
ALK amplification | ||||||||||||||||||||||||||||||||||||||
ALK F1245C | ||||||||||||||||||||||||||||||||||||||
ALK F1174C | ||||||||||||||||||||||||||||||||||||||
ATRX mutation | ||||||||||||||||||||||||||||||||||||||
MYCN positive | ||||||||||||||||||||||||||||||||||||||
MYCN amplification | ||||||||||||||||||||||||||||||||||||||
CD276 expression | ||||||||||||||||||||||||||||||||||||||
TERT rearrangement | ||||||||||||||||||||||||||||||||||||||
PGBD5 overexpression | ||||||||||||||||||||||||||||||||||||||
NRAS Q61K | ||||||||||||||||||||||||||||||||||||||
MYC amplification + ALK F1174L | ||||||||||||||||||||||||||||||||||||||
PGBD5 underexpression | ||||||||||||||||||||||||||||||||||||||
DLL3 underexpression | ||||||||||||||||||||||||||||||||||||||
DLK1 expression | ||||||||||||||||||||||||||||||||||||||
DLL3 expression | ||||||||||||||||||||||||||||||||||||||
ALK rearrangement + ALK R1275Q + TP53 mutation | ||||||||||||||||||||||||||||||||||||||
MYCN amplification + ALK rearrangement | ||||||||||||||||||||||||||||||||||||||
MYCN amplification + ALK F1174V | ||||||||||||||||||||||||||||||||||||||
NF1 underexpression | ||||||||||||||||||||||||||||||||||||||
MYCN amplification + ALK F1174L | ||||||||||||||||||||||||||||||||||||||
MYCN amplification + ALK R1275Q | ||||||||||||||||||||||||||||||||||||||
ETV6-NTRK3 fusion |