Abstract PS4-01-24: Cytokine score based on expression levels of multiple cytokines is a prognostic indicator in metastatic breast cancer patients treated with chemotherapy

Abstract Background: The tumor immune microenvironment affects treatment response and outcomes in patients with metastatic breast cancer (MBC). Cytokines, such as tumor necrosis factor-α (TNF-α) and interleukin (IL)-6, play an important role in tumor progression and immune regulation, and they are associated with outcomes in patients with MBC. Although the significance of each cytokine as a prognostic factor has been reported, there is a paucity of reports on the relationship between the integrated indicator of multiple cytokines and outcomes. In this study, we established an integrated indicator of multiple cytokines and examined the relationship with patient outcomes. In addition, since inflammatory cytokines are thought to affect cancer progression and metastasis by acting on T cells, myeloid-derived suppressor cells (MDSCs), and regulatory T cells (Tregs), we also examined the relationship between the integrated cytokine indicator and immune cell profile. Materials and Methods: This retrospective study included 43 patients with MBC treated with chemotherapy. Baseline values for cytokine levels, including TNF-α, soluble interleukin-2 receptor (sIL-2R), IL-6, IL-8, transforming growth factor (TGF)-β, and thymidine kinase 1 (TK1), were measured in peripheral blood on the day before the first treatment with chemotherapy. Each cytokine was classified into low and high groups using cutoff values defined by ROC curves for overall survival (OS), and the progression-free survival (PFS) and OS between low and high groups were compared by Kaplan-Meier plots. CD4+ and CD8+ lymphocytes, MDSCs, and Tregs levels were determined in the blood by flow cytometry analysis. Results: Of the patients, 46.5% (n = 20) were treated with eribulin, 9.3% (n = 4) with trastuzumab deruxtecan, 9.3% (n = 4) with paclitaxel and bevacizumab, 7.0% (n = 3) with trastuzumab emtansine, and 27.9% (n = 12) with other chemotherapeutic agents. Patients treated as first-line were 55.8% (n = 24), and those treated as second-line or later were 44.2% (n = 19). Patients with high levels of TNF-α, sIL-2R, IL-6, and TK1 showed a shorter OS compared to those with low levels (P = 0.01, 0.01, 0.01, and