Regional chemotherapy for colorectal liver metastases: A phase II evaluation of targeted hepatic arterial 5-fluorouracil for colorectal liver metastases

Author:

Goldberg J A1,Kerr D J2,Wilmott N3,McKillop J H4,McArdle C S1

Affiliation:

1. University Department of Surgery, The Royal Infirmary, Glasgow, UK

2. University Department of Medicine, The Royal Infirmary, Glasgow, UK

3. Cancer Research Campaign Department of Clinical Oncology, University of Glasgow, UK

4. Department of Pharmacy, The University of Strathclyde, Glasgow, UK

Abstract

Abstract The results of systemic chemotherapy in patients with liver metastases from colorectal cancer remain dismal. Regional chemotherapy has been advocated as a method of improving the delivery of cytotoxic drugs to tumour, while minimizing systemic toxicity. The use of vasoactive agents to redistribute arterial blood flow towards tumour, and of biodegradable microspheres to slow tumour blood flow, have also been suggested as methods of further improving tumour exposure to drug. We present 21 patients who received intrahepatic arterial chemotherapy for colorectal liver metastases. Combined treatment (angiotensin II, albumin microspheres and 5-fluorouracil) was administered 4–6 weekly, and bolus 5-fluorouracil was given in the intervening weeks. Toxicity was minimal. Responses were seen in seven patients. Fewer than half of the deaths were from liver metastases; a quarter of the patients died from non-cancer-related causes. Survival was prolonged in the treated group compared with historical controls. These results suggest that this regimen has activity in patients with colorectal liver metastases.

Funder

Ciba Laboratories for the provision of angiolensin II

Publisher

Oxford University Press (OUP)

Subject

Surgery

Reference19 articles.

1. The clinical correlation of an autopsy study of recurrent colorectal cancer;Welch;Ann Surg,1979

2. A retrospective study of the natural history of patients with liver metastases from colorectal cancer;Wood;Clin Oncol,1976

3. Magnetically responsive microspheres and other carriers for the biophysical targeting of antitumour agents;Widder;Adv Pharmacol Chemother,1979

4. Changes in distribution of hepatic blood flow induced by intra-arterial infusion of angiotensin II in human hepatic cancer;Sasaki;Cancer,1985

5. Improved regional selectivity of hepatic arterial BCNU with degradable microspheres;Dakhil;Cancer,1982

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