Literature DB >> 9834826

Tamoxifen in liver disease: potential exacerbation of hepatic dysfunction.

L C Floren1, M F Hebert, A P Venook, V C Jordan, A Cisneros, K A Somberg.   

Abstract

Tamoxifen, a non-steroidal anti-estrogen, has been used successfully for a decade as post-operative adjuvant therapy for breast cancer. Tamoxifen is generally well tolerated with few side effects, especially at the typical dose of 10 mg twice daily. However, hepatic effects have been reported after tamoxifen administration and are usually found to be cholestatic in nature. Although previous reports concentrate on tamoxifen as a probable cause of drug-induced hepatotoxicity, very little attention has been focused on the use of tamoxifen in patients with pre-existing liver dysfunction and the possible need for dose adjustment. We present the case of a 48-year-old woman with an acute exacerbation of her pre-existing liver dysfunction and subsequent elevations of tamoxifen blood levels after approximately one year of tamoxifen therapy for adjuvant treatment of breast cancer. Tamoxifen dosing was adjusted based on serum levels.

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Year:  1998        PMID: 9834826     DOI: 10.1023/a:1008269025294

Source DB:  PubMed          Journal:  Ann Oncol        ISSN: 0923-7534            Impact factor:   32.976


  5 in total

Review 1.  Dose adaptation of antineoplastic drugs in patients with liver disease.

Authors:  Lydia Tchambaz; Chantal Schlatter; Max Jakob; Anita Krähenbühl; Peter Wolf; Stephan Krähenbühl
Journal:  Drug Saf       Date:  2006       Impact factor: 5.606

2.  A case-control study of non-alcoholic fatty liver disease in breast cancer.

Authors:  Ahmet Bilici; Mustafa Ozguroglu; Ismail Mihmanli; Hande Turna; Ibrahim Adaletli
Journal:  Med Oncol       Date:  2007       Impact factor: 3.064

3.  Unusual causes of intrahepatic cholestatic liver disease.

Authors:  Elias E Mazokopakis; John A Papadakis; Diamantis P Kofteridis
Journal:  World J Gastroenterol       Date:  2007-03-28       Impact factor: 5.742

4.  Influence of gender on tamoxifen-induced biochemical changes in serum of rats.

Authors:  Faried Abdel-Kader El-Sayed Hemieda
Journal:  Mol Cell Biochem       Date:  2007-02-06       Impact factor: 3.842

5.  Tissue distribution of 4-hydroxy-N-desmethyltamoxifen and tamoxifen-N-oxide.

Authors:  Jennifer Gjerde; Sara Gandini; Aliana Guerrieri-Gonzaga; Line L Haugan Moi; Valentina Aristarco; Gunnar Mellgren; Andrea Decensi; Ernst A Lien
Journal:  Breast Cancer Res Treat       Date:  2012-05-05       Impact factor: 4.872

  5 in total

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