13.07.2015 Views

Guidelines for Complications of Cancer Treatment Vol VIII Part B

Guidelines for Complications of Cancer Treatment Vol VIII Part B

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Topotecan causes elevation <strong>of</strong> transaminases in fewer than10% <strong>of</strong> patients and significant elevations <strong>of</strong> liver enzymesare uncommon (19).Irinotecan can cause severe transaminitis which is <strong>of</strong>tenreversible.Usually seen in patients with hepatic metastases(20).Miscellaneous Agents:Cisplatin is a rare cause <strong>of</strong> hepatic toxicity, but minor ASTelevations are common at usual therapeutic dose. Cisplatininducedacute hepatic injury is dose related. (21).Oxaliplatin is renally eliminated and can be given to patientswith severe liver dysfunction due to metastatic colorectalcancer (22).L-asparaginase (L-Asp) hydrolyzes L-asparagine in serum.Hepatic toxicity is quite frequent with L-Asp. The mechanism<strong>of</strong> hepatotoxicity involves impaired protein synthesis fromasparagine depletion. Decreased serum levels <strong>of</strong> albumin,ceruloplasmin, haptoglobin, transferring and coagulationfactors II, VII, IX, X, and fibrinogen are common. Moderateelevations <strong>of</strong> aminotransferase, bilirubin, and alkalinephosphatase also occur. These common changes with L-Aspare usually mild and reversible (23).Bortezomib is metabolized by the liver and clearance maydecrease with hepatic impairment. Hyperbilirubinemia andportal vein thrombosis have also been reported (24).Hepatic Veno-Occlusive Disease:High-dose chemotherapy such as tin stem cell transplant mayresult in a specific pattern <strong>of</strong> hepatotoxicity known as VOD.Drugs implicated to cause this includes busulfan ,Cyclophosphamide, Carmustine (BCNU),Lomustine.466

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