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Drug-induced liver injury due to cancer chemotherapeutic agents

Semin Liver Dis. 2014 May;34(2):162-71. doi: 10.1055/s-0034-1375957. Epub 2014 May 31.

Abstract

Drug-induced liver injury (DILI) due to chemotherapeutic drugs is a significant cause of morbidity and mortality. Most cases of chemotherapy-induced hepatotoxicity are idiosyncratic and do not have a unique clinical or histological signature that is distinct from other agents that cause DILI. The major mechanisms underlying chemotherapy-related hepatotoxicity are based on the production of reactive metabolites generated by phase I oxidation reactions, immunological injury, or alterations in mitochondrial function. Underlying liver disease and hepatic involvement by tumor are important modifiers of liver injury, and reversibility is not universal after drug cessation. Chemotherapy can also exacerbate underlying liver disease, particularly hepatitis B, leading to worsening hepatic function. Diagnosing DILI due to chemotherapeutic agents is particularly challenging because competing etiologies, such as hepatotoxicity from other medications, opportunistic infections, radiation therapy, and pre-existing liver disease, are frequent.

Publication types

  • Review

MeSH terms

  • Antibiotics, Antineoplastic / adverse effects
  • Antibodies, Monoclonal, Humanized / adverse effects
  • Antimetabolites, Antineoplastic / adverse effects
  • Antineoplastic Agents / adverse effects*
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents, Alkylating / adverse effects
  • Chemical and Drug Induced Liver Injury / diagnosis*
  • Chemical and Drug Induced Liver Injury / etiology*
  • Chemical and Drug Induced Liver Injury / metabolism
  • Humans
  • Platinum Compounds / adverse effects
  • Protein Kinase Inhibitors / adverse effects*
  • Taxoids / adverse effects
  • Topoisomerase Inhibitors / adverse effects

Substances

  • Antibiotics, Antineoplastic
  • Antibodies, Monoclonal, Humanized
  • Antimetabolites, Antineoplastic
  • Antineoplastic Agents
  • Antineoplastic Agents, Alkylating
  • Platinum Compounds
  • Protein Kinase Inhibitors
  • Taxoids
  • Topoisomerase Inhibitors