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BIOMARKER:

S100A10 overexpression

over1year
Identification of microenvironment features associated with primary resistance to anti-PD-1/PD-L1 + antiangiogenesis in gastric cancer through spatial transcriptomics and plasma proteomics. (PubMed, Mol Cancer)
We report the results of the REGOMUNE phase II study, in which Caucasian patients were administered regorafenib, a multi-tyrosine kinase inhibitor, in combination with avelumab, a PD-L1-targeting monoclonal antibody. Additionally, peripheral biomarker assessments identified elevated levels of cytokines, including CSF-1, IL-4, IL-8, and TWEAK, correlating with adverse clinical outcomes, thereby accentuating the role of macrophage infiltration in mediating resistance. These insights furnish an invaluable foundation for elucidating, and potentially circumventing, resistance mechanisms in current AGC therapeutic paradigms, emphasizing the integral role of tumor microenvironmental dynamics and immune modulation.
Journal • PD(L)-1 Biomarker • IO biomarker
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CXCL8 (Chemokine (C-X-C motif) ligand 8) • CSF1 (Colony stimulating factor 1) • IL4 (Interleukin 4)
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CXCL8 elevation • S100A10 overexpression
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Bavencio (avelumab) • Stivarga (regorafenib)