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Internal medicine journal · Sep 2024
Observational StudyEvaluation of early fluoropyrimidine toxicity in solid organ cancer patients: a retrospective observational study in Australia.
- Cassandra White, Guy Kendall, Tegan Millington, Bern Corcoran, Christine Paul, Rodney J Scott, and Stephen Ackland.
- University of Newcastle, College of Health, Medicine and Wellbeing, School of Medicine and Public Health, Newcastle, New South Wales, Australia.
- Intern Med J. 2024 Sep 1; 54 (9): 150615141506-1514.
BackgroundDespite common global usage, fluoropyrimidine (FP; 5-flurouracil and capecitabine)-related chemotherapy toxicity is poorly reported in the literature, with serious toxicity ranging from 10% to 40% and early toxicity (within 60 days of exposure) quoted at 14%. Data reflecting the incidence of Grades 3-5 FP-related toxicity in Australian cancer patients is scant, despite the significant impact of toxicity on patients (hospitalisations, intensive care unit (ICU) admissions and even death).AimsThis retrospective audit evaluated Grades 3-5 toxicities in a contemporaneous cohort of 500 patients receiving FP chemotherapies within the Hunter-New England Local Health District from June 2020 to June 2022. Data were extracted from public hospital records and oncology-specific e-records to determine rates of toxicity and associated hospitalisations, intensive care admissions and deaths that occurred within 60 days of first exposure to FP chemotherapy-containing regimens.ResultsOne hundred and fifty incidents of Grades 3-4 toxicity in the first 60 days led to 87 patients presenting to hospital (87/500, 17.4%). The most common serious toxicities were diarrhoea (39.3%), nausea and vomiting (22.7%) and febrile neutropaenia (10%). Four patients were admitted to the ICU, and four patients died of toxicity. Within the first 60 days, 22.2% of patients required treatment delays, 21.4% required dose reductions, and 7.8% of patients ceased treatment because of toxicities.Discussion And ConclusionOur experience reflects international reports and is likely generalisable to the Australian population. These data are a basis to understand the potential benefits of precision medicine strategies such as pharmacogenomic screening to improve patient tolerability and the cost-effectiveness of FP chemotherapy prescribing.© 2024 Royal Australasian College of Physicians.
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