Clinical Study
British Journal of Cancer (2007) 96, 546–550. doi:10.1038/sj.bjc.6603590 www.bjcancer.com
Published online 6 February 2007
Treatment of 5-fluorouracil refractory metastatic colorectal cancer: an Australian population-based analysis
D Damianovich1, M Adena2 and N C Tebbutt1
- 1Ludwig Institute for Cancer Research, Austin Health, Melbourne, Victoria, Australia
- 2Covance Pty Ltd, Canberra, Australian Capital Territory, Australia
Correspondence: Dr NC Tebbutt, Ludwig Institute for Cancer Research, Austin Hospital, 145-163 Studley Road, Heidelberg, Victoria 3084, Australia. E-mail: niall.tebbutt@ludwig.edu.au
Received 30 August 2006; Revised 13 December 2006; Accepted 14 December 2006; Published online 6 February 2007.
Abstract
Randomised trials have established the importance of oxaliplatin (O) and irinotecan (I) in advanced colorectal cancer (CRC). However, patients enrolled in clinical studies represent a restricted population and little is known about the use of O and I in the general population and the subsequent outcomes outside clinical studies. We used the Australian Health Insurance Commission (HIC) database to describe prescribing patterns of O and I and their impact on survival in all patients with 5-fluorouracil (5-FU) refractory CRC in Australia in 2002 and 2003. In 2999 patients, there was a marked increase in initial treatment with O rather than I; 48% of patients received O first in 2002 vs 66% in 2003 (P<0.001). Overall 40–45% of patients received both O and I; however, younger patients were more likely to receive both drugs (P<0.001). After 5-FU failure and treatment with O or I, the proportion of patients surviving 6 or 12 months was estimated to be 0.67 (95% CI, 0.66–0.69) and 0.42 (95% CI, 0.40–0.44), respectively. Survival was superior for patients who received both O and I; however, the sequence of agents had no impact. Older patients (
70 years) had inferior survival no matter which drug was used as initial treatment. Analysis of the Australian HIC database provides a valuable means of assessing patterns of use and outcomes of new therapies.
Keywords:
metastatic colorectal cancer, irinotecan, oxaliplatin
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