Treatment of advanced colorectal cancer in a patient with cardiotoxic reactions to 5-fluorouracil and capecitabine using suboptimal doses

A 32-year-old female with stage IV colorectal cancer and metastasis to the liver experienced cardiotoxic reactions after treatment with 5-fluorouracil and its oral prodrug capecitabine even at two-thirds the recommended dose. After careful considerations, the decision was made to attempt capecitabin...

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Veröffentlicht in:BMJ case reports 2017-11, Vol.2017, p.bcr-2017-220952
Hauptverfasser: Cioffi, Joseph H, Estes, Derek J, Florou, Vaia, Ardalan, Bach
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Estes, Derek J
Florou, Vaia
Ardalan, Bach
description A 32-year-old female with stage IV colorectal cancer and metastasis to the liver experienced cardiotoxic reactions after treatment with 5-fluorouracil and its oral prodrug capecitabine even at two-thirds the recommended dose. After careful considerations, the decision was made to attempt capecitabine retrial at a further suboptimal dose with combination chemotherapy where she no longer experienced cardiac events. As a result, the liver tumour shrank and rectal mass stabilised, tumour markers dropped and she underwent surgical resection of both masses. Later there was local recurrence of disease near the previous liver tumour, so the suboptimal capecitabine therapy was restarted without complaint. The patient became a candidate for a NanoKnife procedure, offering a potentially curative therapy. This case report summarises a novel treatment strategy for those patients with advanced colorectal cancer who experience cardiotoxic reactions to fluoropyrimidines, the active agent of gold standard treatment.
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subjects Analgesics
Biopsy
Cancer therapies
Cardiovascular disease
Case reports
Chemotherapy
Colorectal cancer
Female
Liver
Medical imaging
Metastasis
Novel Treatment (New Drug/Intervention
Established Drug/Procedure in New Situation)
Ostomy
Pain
Patients
Risk factors
Systematic review
USA/Canada
White
title Treatment of advanced colorectal cancer in a patient with cardiotoxic reactions to 5-fluorouracil and capecitabine using suboptimal doses
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