Literature DB >> 34873918

Vanishing bile duct syndrome following pembrolizumab infusion: case report and review of the literature.

Maria Gemelli1,2, Marco Carbone3,4, Maria I Abbate1, Maddalena Mancin1, Nicola Zucchini5, Francesca Colonese1, Pietro Invernizzi3,4, Paolo Bidoli1, Diego Cortinovis1.   

Abstract

PD-1/PD-L1 inhibitors demonstrate high efficacy in non-small-cell lung cancer and are now routinely used in clinical practice. Severe immune-related adverse events are reported in about 5% of patients, requiring hospitalization and possibly leading to death. We present a rare case of vanishing bile duct syndrome that arose a few days after the first pembrolizumab infusion. Laboratory tests and radiological imaging studies were performed to orient diagnosis and monitor the disease, while the evidence of ductal loss on the histological sample was pathognomonic for vanishing bile duct syndrome. High-dose steroid therapy and immunosuppressors were administered, resulting in scarce efficacy. Prompt recognition and management of similar conditions is crucial to avoid fatal events. Further studies are needed to investigate new drugs for steroid-refractory conditions.

Entities:  

Keywords:  immune-related adverse events; immune-related hepatitis; immunotherapy; lung cancer; pembrolizumab; vanishing bile duct syndrome

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Year:  2021        PMID: 34873918     DOI: 10.2217/imt-2021-0078

Source DB:  PubMed          Journal:  Immunotherapy        ISSN: 1750-743X            Impact factor:   4.196


  1 in total

1.  Infliximab-Induced Vanishing Bile Duct Syndrome.

Authors:  Michael J Eiswerth; Matthew A Heckroth; Ali Ismail; Dibson D Gondim; Ryan Kaufman
Journal:  Cureus       Date:  2022-02-05
  1 in total

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