Serum diamine oxidase activity derived from response to chemotherapy affects adverse events and serum amino acid levels
Supportive Care in Cancer, ISSN: 1433-7339, Vol: 30, Issue: 11, Page: 9369-9377
2022
- 6Citations
- 20Captures
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Metrics Details
- Citations6
- Citation Indexes6
- Captures20
- Readers20
- 20
Article Description
Purpose: The relationship between activity of the small intestinal villi and the effectiveness of chemotherapy remains unclear. This study aimed to investigate how serum diamine oxidase (DAO) activity affects antitumor effects, adverse events, and amino acid absorption. Methods: We performed a single-center prospective cohort study that enrolled 50 patients with esophageal cancer (EC) receiving docetaxel, cisplatin, and 5-fluorouracil therapy. We determined the cut-off value of serum DAO activity contributing to a response to chemotherapy using a generalized additive model. Additionally, we compared adverse events, inflammatory markers, blood amino acid levels, and quality of life between the high and low DAO activity groups during chemotherapy. Results: The cut-off value of serum DAO activity at the first visit that contributed to a chemotherapy response was 6.5 units/L. Leukopenia and neutropenia of grade ≥ 3 were significantly higher in the DAO low (< 6.5 units/L) group (p = 0.044, 0.017, respectively). Interleukin-6 was significantly lower in the DAO high (≥ 6.5 units/L) group at the first visit and at 4 weeks after the end of chemotherapy (p = 0.039, 0.011, respectively). Glutamine was higher in the DAO high group at all measurement points during chemotherapy. Fatigue was significantly lower in the DAO high group (p = 0.001). Conclusion: Serum DAO activity may be a predictor of the response to chemotherapy in patients with EC. The absorption capacity of amino acids was maintained in the group with high DAO activity, which may have contributed to the anti-inflammatory effect and provided a background for reducing adverse events.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85138174116&origin=inward; http://dx.doi.org/10.1007/s00520-022-07362-2; http://www.ncbi.nlm.nih.gov/pubmed/36112225; https://link.springer.com/10.1007/s00520-022-07362-2; https://dx.doi.org/10.1007/s00520-022-07362-2; https://link.springer.com/article/10.1007/s00520-022-07362-2
Springer Science and Business Media LLC
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