Fax: (617) 414-1831
Original Article
Treatment of the jaundiced patient with breast carcinoma
Case report and alternate therapeutic strategies
Article first published online: 23 FEB 2001
DOI: 10.1002/1097-0142(20010215)91:4<660::AID-CNCR1048>3.0.CO;2-3
Copyright © 2001 American Cancer Society
Additional Information
How to Cite
Gurevich, I. and Akerley, W. (2001), Treatment of the jaundiced patient with breast carcinoma. Cancer, 91: 660–663. doi: 10.1002/1097-0142(20010215)91:4<660::AID-CNCR1048>3.0.CO;2-3
Publication History
- Issue published online: 23 FEB 2001
- Article first published online: 23 FEB 2001
- Manuscript Accepted: 1 NOV 2000
- Manuscript Revised: 17 OCT 2000
- Manuscript Received: 8 MAY 2000
- Abstract
- Article
- References
- Cited By
Keywords:
- liver;
- metastasis;
- hyperbilirubinemia;
- doxorubicin;
- chemotherapy
Although fixed schedule dose reduction is the conventional management for delivering chemotherapeutic agents to patients with hepatic dysfunction, the authors believe that an alternate strategy of dividing the dose over time represents an extension or complement to the current approach.
Abstract
BACKGROUND
Breast carcinoma in the setting of liver metastases and jaundice raises a complex therapeutic dilemma. Not only is the prognosis poor but toxicity related to treatment can be unpredictable due to altered drug clearance. Guidelines built around dose reduction have been suggested but often do not address the varied presentations in clinical medicine. Bilirubin exceeding 5.0 mg% often is considered an absolute contraindication to the administration of chemotherapeutic agents dependent on hepatic metabolism.
METHODS
A 55-year-old woman with metastatic breast carcinoma to the liver and hyperbilirubinemia was treated with sequential, empiric chemotherapy agents with the goal of preventing severe toxicity through dose reduction, avoidance of combination therapy, divided doses (weekly therapy), and selection of drugs less dependent on hepatic clearance. Several attempts did not yield a regimen with a successful response, but toxicity was minimal. Eventually, a successful schedule and dose of an agent cleared by liver metabolism was individualized for the patient.
RESULTS
After eight cycles of low dose weekly doxorubicin chemotherapy, the patient's symptoms resolved, bilirubin level normalized, and performance status returned to baseline. The patient remained on treatment and was alive 12 months later.
CONCLUSIONS
The authors propose that altering a drug schedule by dividing doses may minimize toxicity, maintain dose intensity, and represent an alternative strategy for the treatment of patients with hepatic impairment. Cancer 2001;91:660–3. © 2001 American Cancer Society.

1097-0142/asset/olbannerleft.gif?v=1&s=ca681f5719430b26e1bc15e9ea4c9fc0a7110104)
1097-0142/asset/olbannerright.gif?v=1&s=8142566facf7e76aef9be6c51162a2e920b3b9f9)
1097-0142/asset/cover.gif?v=1&s=a7299bc18f075294c232ade468773cd0672bd470)