Key result
Intravenous 5-FU chemotherapy is linked to severe grade 4 hypertriglyceridemia, confirmed on rechallenge.
Why the study?
While capecitabine is well known to cause clinically relevant hypertriglyceridaemia, 5-fluorouracil is not typically associated with it.
Case Report (n=1)
No
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Intravenous 5-fluorouracil can induce severe, recurrent grade 4 hypertriglyceridaemia even in fluoropyrimidine-naïve patients without baseline dyslipidaemia, warranting consideration of lipid profile monitoring during treatment.
Chemotherapy-induced hypertriglyceridaemia (HTG) is a potential serious adverse event. Severe HTG with triglycerides (TG) >11.3 mmol/L (1000 mg/dL) can cause acute pancreatitis in addition to cardiovascular diseases such as coronary artery disease. While the association of capecitabine (5-fluorouracil (5-FU) prodrug) with clinically relevant HTG is a well-known adverse reaction, 5-FU is not typically associated with HTG. We here report the case of a patient who developed 5-FU-associated grade 4 HTG with TG level raising up to 37.1 mmol/L (3286 mg/dL) occurring after the ninth cycle of adjuvant FOLFOX (Fluorouracil and Oxaliplatin) chemotherapy. Fenofibrate treatment and diet were started. Chemotherapy was postponed and then resumed for two additional cycles. However, severe HTG recurred shortly after. Chemotherapy was therefore permanently stopped. Approximately 8 weeks after chemotherapy discontinuation, TG fell back to range at 2.1 mmol/L (189 mg/dL) allowing interruption of fenofibrate without HTG recurrence at 3 months.
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Moore et al. (2023) conducted a case report in Stage IIIC colon cancer with 5-fluorouracil-associated severe hypertriglyceridaemia (n=1). 5-fluorouracil (within adjuvant FOLFOX chemotherapy) was evaluated on Severe grade 4 hypertriglyceridaemia (serum triglyceride level). Intravenous 5-fluorouracil chemotherapy was associated with severe grade 4 hypertriglyceridaemia (triglycerides 37.1 mmol/L [3286 mg/dL]) with positive rechallenge and resolution after cessation.
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