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Acute temozolomide induced liver injury: Mixed type hepatocellular and cholestatic toxicity

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Acute temozolomide induced liver injury: mixed type hepatocellular and

chole-static toxicity

Cem Aygun

1

,

2 3 1 1

Abstract

Temozolomide (TMZ) is an oral imidazotetrazine methylating agent which is used for the treatment of glioblastoma multiforme (GBM). We report a case of acute hepatotoxicity in a 53-year old male patient after administration of TMZ for GBM. He had fatigue, nausea, anorexia and jaundice. His laboratory analysis showed alanine aminotransferase(ALT): 632 IU/L (normal range 0-40); aspartate aminotransferase(AST): 554 IU/L (normal range 5-34); alkaline phosphatase(ALP): 1143 IU/L (normal range 40-150); -glutamyl transpeptidase(GGT): 514 IU/L (normal range 9-64 IU/L); total bilirubin: 15.1 mg/dL (normal range 0-1.2); direct bilirubin: 13.2 mg/dL and prothrombin time(PT): 13.5 s, with international normalized ratio (INR): 1.1 (normal range 0.8-1.2). His liver biopsy specimen showed mixed-type (both hepatocellular and cholestatic) hepatic injury, compatible with a diagnosis of drug-induced hepatitis. An objective causality assessment using the Naranjo probability scale suggested that TMZ was the probable cause of the acute hepatitis. His liver function tests gradually normalized in 2 months after discontinuation of the drug. In susceptible individuals, TMZ use may lead to acute mixed type liver toxicity. Complete recovery may be possible if the drug is discontinued before severe liver injury is established.

2016, 79, 363-365

Key words : Temozolomide, drug-induced cholestatic hepatitis.

Introduction

Case report

2

2

Acta Gastro-Enterologica Belgica, Vol. LXXIX, July-September 2016

CASE REPORT

(2)

C. Aygun

Acta Gastro-Enterologica Belgica, Vol. LXXIX, July-September 2016

Discussion

Liver biopsy specimen showing cholestasis, steatosis, (HEx100).

Canalicular cholestasis and focal necrosis with

ste-atosis, (HEx200).

(3)

Acute temozolomide induced liver injury

Acta Gastro-Enterologica Belgica, Vol. LXXIX, July-September 2016

References

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N. Engl. J. Med., 349

7th ed. Philadelphia: Saunders

Curr. Treat

Options Gastroenterol., 3

Ann. Intern. Med.,

139

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J. Surg. Oncol., 27

et al

Cancer Gene Ther., 7

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