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Management of liver and gastrointestinal toxicity induced by immune checkpoint inhibitors: Position statement of the AEEH-AEG-SEPD-SEOM-GETECCU

    1. [1] Instituto de Salud Carlos III

      Instituto de Salud Carlos III

      Madrid, España

    2. [2] Hospital Universitario Marqués de Valdecilla

      Hospital Universitario Marqués de Valdecilla

      Santander, España

    3. [3] Hospital General Universitario de Elche

      Hospital General Universitario de Elche

      Elche, España

    4. [4] Hospital Universitario Central de Asturias

      Hospital Universitario Central de Asturias

      Oviedo, España

    5. [5] Instituto de Investigación Sanitaria Gregorio Marañón

      Instituto de Investigación Sanitaria Gregorio Marañón

      Madrid, España

    6. [6] Complexo Hospitalario Universitario de Ourense

      Complexo Hospitalario Universitario de Ourense

      Ourense, España

    7. [7] Hospital Ramón y Cajal

      Hospital Ramón y Cajal

      Madrid, España

  • Localización: Revista Española de Enfermedades Digestivas, ISSN-e 2340-4167, ISSN 1130-0108, Vol. 116, Nº. 2, 2024, págs. 83-113
  • Idioma: inglés
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  • Resumen
    • The development of the immune checkpoint inhibitors (ICI) is one of the most remarkable achievements in cancer therapy in recent years. However, their exponential use has led to an increase in immune-related adverse events (irAEs). Gastrointestinal and liver events encompass hepatitis, colitis and upper digestive tract symptoms accounting for the most common irAEs, with incidence rates varying from 2 % to 40 %, the latter in patients undergoing combined ICIs therapy. Based on the current scientific evidence derived from both randomized clinical trials and real-world studies, this statement document provides recommendations on the diagnosis, treatment and prognosis of the gastrointestinal and hepatic ICI-induced adverse events.


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