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©2014 Baishideng Publishing Group Inc.
World J Gastroenterol. Aug 14, 2014; 20(30): 10288-10295
Published online Aug 14, 2014. doi: 10.3748/wjg.v20.i30.10288
Published online Aug 14, 2014. doi: 10.3748/wjg.v20.i30.10288
Drug | Target | Study | Phase | Objective |
Patients (est.) | (primary, secondary) | |||
Vemurafenib plus | BRAF/EGFR | A Pilot Study of Vemurafenib and Panitumumab Combination Therapy in Patients With BRAF V600E Mutated Metastatic Colorectal Cancer | I/II | ORR |
Panitumumab | n = 15 | PFS/OS | ||
Vemurafenib, Cetuximab plus | BRAF/EGFR plus chemotherapy | A Phase I Trial of Vemurafenib in Combination With Cetuximab and Irinotecan in Patients With BRAF V600 Mutant Advanced Solid Malignancies | I | MTD |
Irinotecan | n = 63 | |||
Dabrafenib, Trametinib panitumumab | BRAF/MEK and EGFR | An Open-Label, Three-Part, Phase I/II Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics, and Clinical Activity of the MEK Inhibitor GSK1120212, BRAF Inhibitor GSK2118436 and the Anti-EGFR antibody Panitumumab in Combination in Subjects With BRAF-mutation V600E or V600K Positive Colorectal Cancer | I/II | DLTs |
n = 200 | Pharmacokinenics | |||
RR | ||||
LGX818 | BRAF | A phase I, multicentre, open label, dose-escalation study of oral LGX818 in adult patients advanced colorectal cancer BRAF mutated | I | DLT |
n = 126 | Tumour response | |||
LGX818 | BRAF | A Phase Ib/II Multi-center, Open-label, Dose Escalation Study of LGX818 and Cetuximab or LGX818, BYL719, and Cetuximab in Patients With BRAF Mutant Metastatic Colorectal Cancer | I/II | DLT |
BYL719 | PI3K | n = 124 | PFS | |
Cetuximab | EGFR | |||
CEP-32496 | BRAF | An open-Label, Phase 1/2, Single-Agent Study of CEP-32496 in Patients With Advanced Solid Tumors in Phase 1 and in Patients With Advanced Melanoma and Metastatic Colorectal Cancer With BRAF Mutation in Phase 2 | I/IIn = 154 | ORRPFS |
BKM120 | PI3K | Phase I Trial of Irinotecan and BKM120 in Previously Treated Advanced Colorectal Cancer | I | MTD |
Irinotecan | plus chemotherapy | n = 30 | Pharmacokinetics | |
BKM120 | PI3K | Phase I/II Study of the P13Kinase Inhibitor BKM120 Given in Combination With Panitumumab in Patients With Metastatic or Advanced RAS-Wild Type Colorectal Cancer | I/II | MTD |
n = 40 | Antitumour activity | |||
Panitumumab | EGFR | Translational research | ||
GSK- 2636771 | PI3K-beta | A Phase I/IIa, First Time in Human, Open-label Dose-escalation Study of GSK2636771 in Subjects With Advanced Solid Tumors With PTEN Deficiency | I/II | MTD |
n = 150 | Pharmacokinetics | |||
Efficacy | ||||
BKM120 | PI3K | A Phase Ib, Open-label, Multi-center, Dose-escalation and Expansion Study of an Orally Administered Combination of BKM120 Plus MEK162 in Adult Patients With Selected Advanced Solid Tumors | I | Rate of DLTs |
MEK162 | MEK | n = 88 | ORR and PFS | |
MK-2206 | Akt | A Phase 2 Study of MK-2206 in Previously Treated Metastatic Colorectal Cancer Patients Enriched for PTEN Loss and PIK3CA Mutation | II | ORR |
n = 54 | Biomarker validation | |||
MK-2206 | Akt | Pilot Study of the Combination of MK-2206, an AKT Inhibitor, and AZD6244, a MEK Inhibitor, in Patients With Advanced Colorectal Carcinoma | II | Evaluate reduction of pAKT, pERK and Ki-67 |
Selumetinib | MEK | n = 38 | ||
Everolimus | mTOR | Phase I/Randomized Phase II Study of Second Line Therapy With Irinotecan and Cetuximab With or Without RAD001, an Oral mTOR Inhibitor for Patients With Metastatic Colorectal Cancer | I/II | MTD |
Irinotecan | EGFR | n = 41 | ORR | |
Cetuximab | plus chemotherapy | |||
SAR245408 (XL147) | mTOR | A Phase 1 Dose Escalation Study of Combination Therapy With Oral SAR245408 (XL147) and Oral MSC1936369B in Patients With Locally Advanced or Metastatic Solid Tumors | I | MTD |
MSC 1936369B | MEK | n = 170 | Pharmacokinetics | |
Onartuzumab | c-MET | Randomized, Double-Blind, Phase II Study of FOLFOX/Bevacizumab With Onartuzumab (MetMAb) vs Placebo as First-Line Treatment for Patients With Metastatic Colorectal Ca | II | PFS |
Bevacizumab | VEGF-A | n = 196 | Response rate | |
FOLFOX | plus chemotherapy | |||
Trastuzumab | HER2 | A Phase II multi-center 2-sequential cohorts trial, designed to assess the objective response rate of the anti HER2 monoclonal antibody trastuzumab, used in combination with either the small molecule tyrosine kinase inhibitor lapatinib (Cohort A) or the monoclonal antibody pertuzumab (Cohort B), in advanced disease CRC patients harbouring an amplified HER2 tumor | II | ORR |
Pertuzumab | EGFR | n = 54 | PFS | |
Lapatinib | ||||
Olaparib | PARP | Phase II, Open-Label, Multicenter Trial to Assess the Efficacy and Safety of the PARP Inhibitor, Olaparib, Alone in Previously-Treated Patients With Stage IV, Measurable Colorectal Cancer, Stratified by MSI Status | II | Tumour response |
n = 33 | ||||
ABT-888 | PARP | A Phase I Study of ABT-888 in Combination With Oxaliplatin and Capecitabine in Advanced Solid Tumors | I | MTD/DLTs |
Oxaliplatin | n = 36 | Pharmacokinetics | ||
Capecitabine | Tumour response | |||
Brivanib Alaninate | VEGFR | A phase II Study of second-line irinotecan plus brivanib, a dual tyrosine inhibitor of VEGFR and FGFR, in metastatic colorectal cancer patients enriched for elevated levels of plasma FGF following progression on bevacizumab-based treatment | II | PFS |
Irinotecan | FGFR plus chemotherapy | n = 60 |
- Citation: Spiliopoulou P, Arkenau HT. Rationally designed treatment for metastatic colorectal cancer: Current drug development strategies. World J Gastroenterol 2014; 20(30): 10288-10295
- URL: https://www.wjgnet.com/1007-9327/full/v20/i30/10288.htm
- DOI: https://dx.doi.org/10.3748/wjg.v20.i30.10288