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Drug resistance and new therapies in colorectal cancer

World Journal of Gastroenterology · 2018 · Vol. 24(34) · pp. 3834–3848
Kevin Van der JeughtHan-Chen XuYu-Jing LiXiong-Bin LuGuang Ji

Abstract

Colorectal cancer (CRC) is often diagnosed at an advanced stage when tumor cell dissemination has taken place. Chemo- and targeted therapies provide only a limited increase of overall survival for these patients. The major reason for clinical outcome finds its origin in therapy resistance. Escape mechanisms to both chemo- and targeted therapy remain the main culprits. Here, we evaluate major resistant mechanisms and elaborate on potential new therapies. Amongst promising therapies is α-amanitin antibody-drug conjugate targeting hemizygous p53 loss. It becomes clear that a dynamic interaction with the tumor microenvironment exists and that this dictates therapeutic outcome. In addition, CRC displays a limited response to checkpoint inhibitors, as only a minority of patients with microsatellite instable high tumors is susceptible. In this review, we highlight new developments with clinical potentials to augment responses to checkpoint inhibitors.

Colorectal Cancer Treatments and StudiesHepatocellular Carcinoma Treatment and PrognosisHepatitis B Virus StudiesColorectal cancerMedicineDrug resistanceDrugOncologyMicrosatellite instabilityTargeted therapyTumor microenvironmentCancerAntibody-drug conjugate

MeSH terms

Antineoplastic Agents, ImmunologicalHumansImmunotherapyRNA Polymerase IIColorectal NeoplasmsTumor Suppressor Protein p53Treatment OutcomeImmunoconjugatesDrug Resistance, NeoplasmTumor EscapeNucleic Acid Synthesis InhibitorsMicrosatellite InstabilityAlpha-AmanitinTumor MicroenvironmentCostimulatory and Inhibitory T-Cell Receptors

Funding

  • National Natural Science Foundation of China
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