Table 2:
Drug Description | NA | Phase I | Phase I/II | Phase II | Phase III | Total | |
---|---|---|---|---|---|---|---|
Number of Trials | 1 | 9 (14%) | 8 (12%) | 39 (60%) | 8 (12%) | 65 (100%) | |
Combination Strategy | |||||||
Chemotherapy Agents (≥2) | - | 4 | 5 | 26 | 5 | 40 (62%) | |
Chemotherapy + WBRT | 1 | 4 | - | 9 | 1 | 15 (23%) | |
Chemotherapy + SRS | - | 1 | 2 | 2 | - | 5 (8%) | |
Chemotherapy + WBRT or SRS | - | - | 1 | - | - | 1 (2%) | |
Chemotherapy + Surgery | - | - | - | - | 1 | 1 (2%) | |
WBRT + SRS | - | - | - | 1 | 1 | 2 (3%) | |
Chemo + Diet | - | - | - | 1 | - | 1 (2%) | |
Therapeutic Agents | |||||||
Abemaciclib | CDK inhibitor | - | 1 | - | - | - | 1 (2%) |
Afatinib | Tyrosine kinase inhibitor | - | - | - | 1 | - | 1 (2%) |
Atezolizumab | PD-L1 inhibitor | - | - | - | 2 | 2 | 4 (6%) |
Bevacizumab | VEGF-A inhibitor | - | - | - | 5 | - | 5 (8%) |
BKM120 | PI3K inhibitor | - | - | 1 | 1 | - | 2 (3%) |
Cabazitaxel | Taxane, microtubule inhibitor | - | - | - | 1 | - | 1 (2%) |
Cabozantinib | Tyrosine kinase inhibitor | - | - | - | 1 | - | 1 (2%) |
Caelyx | Topoisomerase inhibitor | - | - | - | 1 | - | 1 (2%) |
Capecitabine | Thymidylate synthase inhibitor | - | 1 | - | 8 | 1 | 10 (15%) |
Carboplatin | Alkylating agent, Cross-links DNA | - | - | 1 | 1 | - | 2 (3%) |
Cisplatin | Alkylating agent, Cross-links DNA | - | - | - | 4 | - | 4 (6%) |
Cytarabine | DNA polymerase inhibitor | - | - | - | 1 | - | 1 (2%) |
Docetaxel | Taxane, microtubule inhibitor | - | - | - | 2 | - | 2 (3%) |
Durvalumab | PD-1 inhibitor | 1 | - | - | - | - | 1 (2%) |
Efaproxiral | Propanoic acid | - | - | - | - | 1 | 1 (2%) |
Etoposide | Topoisomerase inhibitor | - | - | - | 2 | - | 2 (3%) |
Everolimus | mTOR inhibitor | - | - | 1 | 2 | - | 3 (5%) |
Galinpepimut-S | WT1 peptide vaccine | - | - | 1 | - | 1 (2%) | |
GDC-0084 | PI3K inhibitor | - | - | - | 1 | - | 1 (2%) |
Gemcitabine | Nucleoside analog | - | - | - | 1 | - | 1 (2%) |
GRN1005 | Taxane, microtubule inhibitor | - | - | - | 1 | - | 1 (2%) |
GW572016 | Tyrosine kinase inhibitor | - | - | - | - | 1 | 1 (2%) |
Indinavir+Ritonavir | Protease inhibitors | - | - | - | 1 | - | 1 (2%) |
Iniparib | PARP inhibitor | - | - | - | 1 | - | 1 (2%) |
Irinotecan | Topoisomerase inhibitor | - | - | - | 4 | - | 4 (6%) |
Lapatinib | Tyrosine kinase inhibitor | - | 3 | 1 | 7 | 2 | 13 (20%) |
Letrozole | Aromatase inhibitor | - | - | - | - | 1 | 1 (2%) |
Methotrexate | Dihydrofolate reductase inhibitor | - | - | 1 | 1 | - | 2 (3%) |
Nivolumab | PD-1 inhibitor | - | 1 | - | - | - | 1 (2%) |
ONC201 | Dopamine receptor antagonist | - | - | - | 1 | - | 1 (2%) |
Paclitaxel | Taxane, microtubule inhibitor | - | - | - | 1 | 1 | 2 (3%) |
Peginterferon Alfa-2a | Alpha interferon | - | - | - | 1 | - | 1 (2%) |
Pembrolizumab | PD-1 inhibitor | - | - | 2 | - | - | 2 (3%) |
Pertuzumab | HER-dimerization inhibitor | - | - | - | 2 | 1 | 3 (5%) |
Pyrotinib | Tyrosine kinase inhibitor | - | - | - | 2 | - | 2 (3%) |
RO4929097 | Gamma secretase inhibitor | - | - | 1 | - | - | 1 (2%) |
Sorafenib | RAF kinase inhibitor | - | 1 | - | - | - | 1 (2%) |
Sunitinib | Tyrosine kinase inhibitor | - | - | - | 1 | - | 1 (2%) |
TDM-1 | HER-dimerization inhibitor/microtubule inhibitor | - | 1 | - | - | - | 1 (2%) |
Temozolomide | Alkylating agent | - | 1 | 2 | 3 | - | 6 (9%) |
Tesevatinib | Tyrosine kinase inhibitor | - | - | 1 | - | - | 1 (2%) |
Topotecan | Topoisomerase inhibitor | - | - | - | 1 | - | 1 (2%) |
Trastuzumab | HER2 receptor inhibitor | - | 2 | 4 | 10 | 3 | 19 (29%) |
Tremelimumab | CTLA-4 inhibitor | 1 | - | - | - | - | 1 (2%) |
Tucatinib | HER2 receptor inhibitor | - | 2 | - | 1 | 1 | 4 (6%) |
Veliparib | PARP inhibitor | - | - | - | 1 | - | 1 (2%) |
Vinorelbine | Vinca alkaloid, tubulin inhibitor | - | - | - | 3 | 1 | 4 (6%) |
Vorinostat | Histone deacetylase inhibitor | - | 1 | - | - | - | 1 (2%) |
WBRT: whole brain radiation therapy, SRS: stereotactic radiosurgery.