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Guidelines for Complications of Cancer Treatment Vol VIII Part B

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Vincristine: No dose reduction if bilirubin < 1.5 mg/dL andSGOT < 60 mg/dL.Reduce by 50% if bilirubin 1.5–3.0 mg/dL and SGOT 60–180 mg/dL. Omit if bilirubin > 3.0 mg/dL or SGOT > 180mg/dL.N/A– not available. ULN– upper limit <strong>of</strong> normal.Bibliography1. Ishak KG, Zimmerman HJ. Morphologic spectrums <strong>of</strong>drug-induced liver disease. Gastroenterol Clin North Am1995;24:759-786.2. Lee WM. Drug-induced hepatotoxicity. N Engl J Med1995; 333: 1118-1127.3. Goldberg JW, Lidsky MD. Cyclophosphamideassociated hepatotoxicity. South Med J 1985; 78:222-223.4. Rodriquez V, Bodey GP, Freireich EJ, et al. Reduction<strong>of</strong> ifosfamide toxicity using dose fractionation. <strong>Cancer</strong>Res 1976; 36:2945-2948.5. Lazarus HM, Herzig RH, Graham Pole J, et al. Intensivemelphalan chemotherapy and cryopreserved autologousbone marrow transplantation in the treatment <strong>of</strong>refractory cancer. J Clin Oncol 1983; 1:359-367.6. Morris LE, Guthrie TH. Busulfan induced hepatitis. AmJ Gastroenterol 1988;83: 682-683.7. Stephen C. Medlin Michael C. Perry. In Michael C. Perryeds. Chemotherapy Source Book, 4th Edition ,Lippincott Williams & Wilkins 2008 : 212- 213.8. RE Slavin, MA Dias and R Saral, Cytosine arabinosideinduced gastrointestinal toxic alterations in sequentialchemotherapeutic protocols: a clinical-pathologic study<strong>of</strong> 33 patients, <strong>Cancer</strong> 42 (1978), pp. 1747–1759.469

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