Effect of Liver Dysfunction on S-1 Therapy Induced Adverse Effects: A Retrospective Cohort Study
View abstract on PubMed
Summary
This summary is machine-generated.Elevated total bilirubin (T-Bil) levels in patients receiving S-1 chemotherapy correlate with decreased platelet counts. This suggests S-1 administration may cause thrombocytopenia in patients with liver dysfunction.
Area Of Science
- Oncology
- Pharmacology
- Hepatology
Background
- Renal dysfunction often requires S-1 dose reduction.
- Decreased dihydropyrimidine dehydrogenase (DPD) activity can cause adverse events with 5-FU.
- Current guidelines use total bilirubin (T-Bil) ≤1.5x ULN for S-1 safety, but the link to liver dysfunction and dose reduction is unclear.
Purpose Of The Study
- To investigate the relationship between liver dysfunction, indicated by T-Bil levels, and S-1 dose reduction.
- To determine the clinical outcomes associated with varying T-Bil levels in patients undergoing S-1 monotherapy.
Main Methods
- Retrospective analysis of 883 patients receiving S-1 monotherapy.
- Patients categorized into Low T-Bil (≤2.25) and High T-Bil (>2.25) groups.
- Primary outcome: variation in blood sampling results; analyzed clinical outcomes including RBC and PLT counts.
Main Results
- 883 patients and 7,511 treatment instances analyzed; 7,245 in Low T-Bil, 266 in High T-Bil group.
- Significant correlations found between T-Bil group and RBC count, PLT count, and T-Bil level.
- High T-Bil group showed significant decreases in RBC and PLT counts compared to the Low T-Bil group.
Conclusions
- S-1 administration in patients with liver dysfunction and elevated T-Bil may lead to thrombocytopenia.
- Monitoring T-Bil levels is crucial for managing S-1 therapy in patients with liver impairment.
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