Review
Copyright ©The Author(s) 2023.
World J Gastroenterol. Feb 14, 2023; 29(6): 926-948
Published online Feb 14, 2023. doi: 10.3748/wjg.v29.i6.926
Table 1 Strategies to reverse targeted therapy resistance in clinical trials
Target(s)
Agent(s)
Phase
Condition
Treatment
Main outcomes
EGFR ECDSym004Phase IKRAS-WT mCRCSym004mOS: 12.8 mo
EGFR S468RNecitumumabPhase IIFirst-line mCRCNecitumumab + mFOLFOX6ORR: 63.6%
KRASG12CSotorasib (AMG 510)Phase ISolid tumorsSotorasibORR: 7.1%; DCR: 73.8%
KRASG12CAdagrasib (MRTX849)Phase IISolid tumorsAdagrasibORR: 17%; DCR: 94%
BRAFVemurafenibPilot trialPreviously treatedVemurafenib + panitumumabDCR: 83%
BRAFVemurafenibPhase IPreviously treatedIrinotecan + vemurafenibORR: 35%; DCR: 88%; mPFS: 7.7m
BRAFVemurafenibSWOG-S1406; phase IIPreviously treatedIrinotecan + cetuximab + vemurafenibmPFS: 4.2 mo; ORR: 17%; DCR: 65%
BRAFEncorafenibBEACON; phase IIIPreviously treatedEncorafenib + binimetinib + cetuximabmOS: 9.3; ORR: 26.8%
BRAFDabrafenibPhase I/IIBRAF-WTDabrafenib + trametinibORR: 12%
HER2Dual-targeted drugsHERACLE A; phase IIKRAS-WTTrastuzumab + lapatinibmOS: 11.5 mo; mPFS: 5.0 mo; ORR: 30%
HER2Pertuzumab; T-DM1HERACLE B; phase IIKRAS/BRAF-WTPertuzumab + trastuzumabORR: 9.7%; mPFS: 4.1 mo
HER2Trastuzumab pertuzumabMyPathway; phase IIPreviously treatedTrastuzumab + pertuzumabORR: 32%; mOS: 11.5 mo; mPFS: 2.9 mo
HER2Trastuzumab pertuzumabTRIUMPH;phase IIKRAS-WTTrastuzumab + pertuzumabORR: 30%; mOS: 10.1 mo; mPFS: 4.0 mo
HER2ADCDESTINY-CRC01; phase IIPreviously treatedTrastuzumab deruxtecan (T-DXd)ORR: 45.3%; mOS: 15.5 mo; mPFS: 6.9 mo
HER2TucatinibMOUNTAINEER; phase IIPreviously treatedTucatinib + trastuzumabORR: 52%; mOS: 18.7 mo; mPFS: 8.1 mo
METTivantinibPhase IIKRAS WT; previously treatedTivantinib + irinotecan + cetuximabmPFS: 8.3 mo; ORR: 44%; mOS: 19.8 mo
EGFR rechallengeIrinotecanCRICKET; phase IIKRAS/BRAF WT; third-lineIrinotecan + cetuximabORR: 21%; DCR: 54%; mOS: 9.8 mo; mPFS: 3.4 mo
EGFR rechallengeAvelumabCAVE; phase IIKRAS WT; third-lineAvelumab + cetuximabmOS: 11.6 mo; mPFS: 3.6 mo; ORR: 7.8%; DCR: 65%
EGFR rechallengeIrinotecanREMARRY and PURSUIT; phase IIKRAS/BRAF WTPanitumumab + irinotecanORR: 14%; mPFS: 3.6 mo
VEGFVanucizumabPhase ISolid tumorsVanucizumabDCR: 59.8%; mPFS: 2.8 mo
VEGFBevacizumabTRIBE; phase IImCRCBevacizumab + FOLFOXIRImPFS: 12.1 mo; mOS: 30.9 mo
VEGFAfliberceptVALOUR; phase IIIPreviously treatedAflibercept + FOLFIRImOS: 13.5 mo; mPFS: 6.9 mo
VEGFAfliberceptAFFIRM; phase IIFirst-lineAflibercept + FOLFOXmPFS: 8.48 mo; 12mPFS: 25.8%
VEGFRamucirumabRAISE; phase IIISecond-lineRamucirumab + FOLFIRImOS: 13.3 mo
VEGFBevacizumabC-TASK FORCE; phase I/IIPreviously treatedBevacizumab + trifluridine/tipiracil16 wk PFS: 46.9%
TKIFamitinibPhase IIPreviously treatedFamitinibmPFS: 2.8 mo; mOS: 7.4 mo; DCR: 59.8%; ORR: 2.2%
NTRKLarotrectinibNAVIGATE; phase I/IISolid tumorsLarotrectinibORR: 50%; DCR: 100%; mPFS: 5.5 mo; mOS: 29.4 mo
PD-1/PD-L1PembrolizumabKEYNOTE-177; phase IIIdMMR/MSI-H CRC; first-linePembrolizumabmPFS: 16.5 mo; mOS: NA
PD-1/PD-L1NivolumabCheckMate-142; phase IIdMMR/MSI-H CRC; previously treatedNivolumabORR: 60%; DCR: 84%
PD-1/PD-L1DurvalumabPhase ISolid tumorsDurvalumab + tremelimumabDCR: 36.4%
PD-1/PD-L1DurvalumabPhase Ib/IIMSS RAS/BRAF WTDurvalumab + tremelimumab + FOLFOXORR: 81%; DCR: 89%
PD-1/PD-L1NivolumabPhase IbMSSNivolumab + regorafenibmPFS: 7.9 mo
PD-1/PD-L1DurvalumabPhase IIChemotherapy-refractory MSSDurvalumab + tremelimumab + radiotherapyORR: 8.3%; mPFS: 1.8 mo; mOS: 11.4 mo