- Case report
- Open Access
- Open Peer Review
Imatinib-induced liver cirrhosis in a patient with advanced gastrointestinal stroma tumor (GIST)
© Seidel et al.; licensee BioMed Central Ltd. 2012
- Received: 4 October 2011
- Accepted: 21 May 2012
- Published: 21 May 2012
The use of imatinib mesylate is associated with a progression free survival of 41 months in first line treatment of metastatic or locally advanced gastrointestinal stromal tumors (GIST) and other studies approved that adjuvant imatinib treatment improves the recurrence-free survival in patients with GIST. Current recommendations include 1 year adjuvant treatment in GIST patients at risk but active studies explore different durations of treatment with an interval of up to 5 years. While the most frequent adverse events (AEs) are blood count alterations, abdominal discomfort and edema, the occurrence of grade 3 or 4 increase of AST or ALT is specified with 2.1% and 2.7% respectively.
We report a 49-year old male with a gastrointestinal stromal tumor (GIST) of the small bowel who developed liver cirrhosis under adjuvant imatinib treatment.
Our report supports the notion that imatinib-induced hepatotoxicity may lead to acute liver damage with subsequent cirrhotic remodelling. Patients developing grade 3 or 4 hepatotoxicity during imatinib treatment should therefore be carefully evaluated for chronic liver disease.
- Liver cirrhosis
The selective tyrosine kinase inhibitor imatinib mesylate has dramatically influenced the treatment of chronic myeloid leukemia (CML) and gastrointestinal stromal tumors (GIST). First line treatment of metastatic or locally advanced GIST with imatinib is currently associated with a PFS of 41 months . The basis for imatinib in the treatment of GIST has been further broadened by other studies, which showed that adjuvant treatment with imatinib improves the recurrence-free survival in patients with GIST [2, 3]. As imatinib treatment is commonly well tolerated, the most frequent adverse events (AEs) are blood count alterations, abdominal discomfort and edema. The adjuvant Z9100 GIST trial reported on grade 3 or 4 increase of AST or ALT in 2.1% and 2.7% respectively, indicating the rather rare occurrence of hepatotoxicity . With the implementation of imatinib for adjuvant treatment in GIST more patients are exposed to imatinib, which may also increase the occurrence of imatinib-induced liver damage. Current recommendations include 1 year adjuvant treatment in GIST patients at risk, but active studies explore different durations of treatment with an interval of up to 5 years duration. We report on a case with liver cirrhosis in a patient with advanced GIST and high-risk of recurrence during adjuvant treatment with imatinib.
To our knowledge this is the first case, which reports on the development of liver cirrhosis during adjuvant imatinib treatment in a patient with GIST. Hepatotoxicity has been observed in about 2–5% of patients receiving imatinib [4–6]. Most of them present with mild temporary liver enzyme elevations, which resolve after dose reductions or discontinuation of imatinib treatment [7, 8]. However, acute liver failure has also been reported sporadically during imatinib treatment [9–11]. Histologic changes have been described in some of these cases and consist of inflammation, fatty degeneration, or necrosis of the liver [10, 12, 13]. Due to the transient nature of toxicity, re-exposure to imatinib is warranted in most cases . Prospective studies in patients with pre-existing liver disease showed that imatinib can be administered safely in these patients, indicating a different mechanism for hepatic toxicity [15, 16]. However, late changes have been recognized in a patient with CML who was diagnosed with liver cirrhosis one year after cessation of treatment due to imatinib-induced acute liver failure . Therefore a close follow up should be mandatory. In asymptomatic patients constant liver enzyme measurements should be adequate. If cirrhotic changes already occurred, liver enzyme quantifications every 3 months with ultrasound of the abdomen and Alpha-Fatal Protein measurements twice a year are performed at our institution. If signs of consecutive liver damage without evident morphological changes of the parenchyma occur, transient elastography could represent an elegant screening method .
As we move forward to adjuvant therapy in GIST, a much larger proportion of patients will receive drug exposure and currently the ideal duration of adjuvant imatinib treatment in high risk GIST remains undefined. The work of Dematteo et al. indicates that the recurrence free survival seems to adapt after a treatment free interval of 18 months. To determine the ideal period of adjuvant imatinib treatment prospectively, clinical trials are conducted to test the efficacy of a prolonged exposure to adjuvant imatinib treatment in GIST for 5 years (NCT00867113) or to evaluate the effects of 12 months versus 36 months (NCT00116935).
Our report supports the notion that chronic liver disease can be a consequence of imatinib-induced hepatotoxicity. In consequence a careful follow-up strategy should be implemented for patients with grade 3 or 4 hepatic toxicity.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
Publication was assisted by the project "Open-Access-Publizieren" of the Deutsche Forschungsgemeinschaft (DFG).
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- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/12/186/prepub
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