Navigating liver toxicity in the age of novel oncological agents

Mar Riveiro-Barciela1,2,3,4, Eleonora De Martin4,5

  • 1Liver Unit, Internal Medicine Department, Hospital Universitari Vall d'Hebron, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.

Insights

Novel cancer therapies improve survival but cause unique liver injury (hepatotoxicity). This review synthesizes knowledge on managing drug-induced liver injury in cancer patients, balancing treatment efficacy with liver health.

Area of Science:

  • Oncology
  • Hepatology
  • Pharmacology

Background:

  • Novel cancer therapies like immune checkpoint inhibitors, antibody-drug conjugates, and protein kinase inhibitors have transformed patient outcomes.
  • These advancements introduce new challenges, notably unpredictable drug-induced liver injury (hepatotoxicity).

Purpose of the Study:

  • To synthesize current knowledge on liver injury associated with key novel oncological agents.
  • To focus on mechanisms, clinical presentation, and management strategies for oncological hepatotoxicity.

Main Methods:

  • Comprehensive literature review of immune checkpoint inhibitors, antibody-drug conjugates, and protein kinase inhibitors.
  • Analysis of drug mechanisms, hepatotoxicity profiles, and clinical management approaches.

Main Results:

  • Novel therapies present unique hepatotoxicity profiles requiring careful monitoring.
  • Combination regimens increase the complexity of drug-liver interactions.

Conclusions:

  • Management of drug-induced liver injury in cancer patients requires balancing oncological efficacy with hepatic preservation.
  • Interdisciplinary collaboration between hepatologists and oncologists is crucial for patient safety.

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