Regorafenib-induced hyperammonemic encephalopathy

J C Kuo1, S Parakh, D Yip

  • 1Department of Medical Oncology, The Canberra Hospital, Garran, ACT, Australia.

Abstract

Insights

Regorafenib, a cancer drug, may cause hyperammonemic encephalopathy in patients with metastatic gastrointestinal stromal tumors (GIST). This condition, marked by confusion and high ammonia levels, resolved upon drug withdrawal.

Area of Science:

  • Oncology
  • Pharmacology
  • Neurology

Background:

  • Regorafenib is a multitargeted tyrosine kinase inhibitor (TKI) used for metastatic gastrointestinal stromal tumors (GIST).
  • Expected adverse events of regorafenib are similar to other TKIs like imatinib, sunitinib, and sorafenib.
  • Metastatic GIST treatment often involves late-line therapies such as regorafenib.

Observation:

  • A 61-year-old male patient with metastatic GIST on regorafenib presented with acute confusion.
  • Confusion resolved upon discontinuation of regorafenib.
  • Confusion and hyperammonemia recurred upon re-initiation of regorafenib, resolving again after cessation.

Findings:

  • This case demonstrates a probable relationship between regorafenib and metabolic encephalopathy.
  • The patient experienced reversible hyperammonemic encephalopathy.
  • Withdrawal and re-challenge with regorafenib correlated with the patient's confusional state and hyperammonemia.

Implications:

  • Regorafenib may induce hyperammonemic encephalopathy, a potential adverse effect not previously reported.
  • A class effect for metabolic encephalopathy among multitargeted TKIs may be postulated.
  • Clinicians should consider monitoring for metabolic encephalopathy in patients treated with regorafenib or similar TKIs.

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