Hepatic Arterial Chemotherapy in Combination with Systemic Chemotherapy Compared with Hepatic Arterial Chemotherapy Alone for Liver Metastases from Colorectal Cancer: Results of a Multi-centric Randomized Study
Hepatic arterial infusion (HAI) chemotherapy is accepted to be an option in patients with non-resectable metastases from colorectal cancer confined to the liver. In a multi-istitutional trial, 76 patients were randomly assigned to receive HAI versus HAI plus systemic bolus 5-fluorouracil and leucovo...
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Veröffentlicht in: | In vivo (Athens) 2006-11, Vol.20 (6A), p.707 |
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Sprache: | eng |
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Zusammenfassung: | Hepatic arterial infusion (HAI) chemotherapy is accepted to be an option in patients with non-resectable metastases from colorectal
cancer confined to the liver. In a multi-istitutional trial, 76 patients were randomly assigned to receive HAI versus HAI
plus systemic bolus 5-fluorouracil and leucovorin. The primary end-point was survival, followed by response, recurrence and
toxicity. Survival was longer for HAI plus systemic chemotherapy (HAI+SYC) than HAI (median, 20 vs. 14 months; p=0.0033),
as were responses (47.5% and 41.7%; p=0.09) and time to hepatic progression (12 vs. 8 months; p=0.039). Side effects included
haematological toxicity that was mostly mild and reversible in 432 cases. Neutropenia grade 3 occurred in four patients in
the HAI+SYC arm and one in the HAI arm. Diarrhoea occurred in 20% and 7% of patients and stomatitis occurred in 18% and 2%,
respectively. On the contrary biliary toxicity was significant; twelve patients had evidence of bilirubin elevations of more
than 3 mg/dl (six in each arm), and two had asymptomatic arterial biliary-tree fistulae: one in the HAI+SYC arm and one in
the HAI arm. Grade 3 elevation in alkaline phosphatase and aminotransferase levels occurred in 26% and 24%, respectively.
In conclusion, the combination of HAI+SYC is active and safe showing a clinical advantage with respect to simple HAI, increasing
overall survival, response rate and time to progression. |
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ISSN: | 0258-851X 1791-7549 |