Indole 3-acetate and response to therapy in borderline resectable or locally advanced pancreatic cancer
Braadland, Peder Rustøen; Farnes, Ingvild; Kure, Elin Wenche Hegland; Yaqub, Sheraz; McCann, Adrian; Ueland, Per Magne; Labori, Knut Jørgen; Hov, Johannes Espolin Roksund
Peer reviewed, Journal article
Published version
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https://hdl.handle.net/11250/3177090Utgivelsesdato
2024Metadata
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Originalversjon
Braadland, P. R., Farnes, I., Kure, E. H., Yaqub, S., McCann, A., Ueland, P. M., Labori, K. J., & Hov, J. R. (2024). Indole 3-acetate and response to therapy in borderline resectable or locally advanced pancreatic cancer. Frontiers in Oncology, 14. Artikkel 1488749. https://doi.org/10.3389/fonc.2024.1488749Sammendrag
Background/Aims: It was recently reported that a higher concentration of the bacterially produced metabolite indole 3-acetate (3-IAA) in blood was linked to a better response to chemotherapy in patients with metastatic pancreatic ductal adenocarcinoma (PDAC). Here, we aimed to extend these observations to patients diagnosed with non-metastatic PDAC.
Method: We measured circulating 3-IAA in samples from a prospective population-based cohort of 124 patients with borderline resectable or locally advanced PDAC, collected before initiating neoadjuvant chemotherapy. The majority (61%) of the patients were treated with FOLFIRINOX. We used univariable and multivariable Cox proportional hazards regression to estimate the association between pre-treatment 3-IAA and overall survival.
Results: The median serum 3-IAA concentration before chemotherapy was 290 (interquartile range 203–417) ng/mL. The unadjusted hazard ratio (HR) for pre-treatment log2(3-IAA) was 0.93, 95% confidence interval (CI) [0.74–1.16], p=0.52. When adjusting for age, ECOG, CA19-9 and tumor classification, the HR for log2(3-IAA) was 0.87, 95% CI [0.68–1.12], p=0.28.
Conclusion: Our findings suggest that the potentiating effect of 3-IAA observed in metastatic PDAC undergoing chemotherapy may not translate to borderline resectable or locally advanced PDAC. We recommend additional clinical validation of 3-IAA’s predictive value in different categories of PDAC before implementation attempts in human studies are initiated