A direct PFS association analysis in the NRF2 high versus NRF2 low subgroups in the tislelizumab plus chemotherapy arm showed a trend similar to the NRF2 mutation status analysis results, although this was not statistically significant (HR = 0.90, 95% CI 0.50–1.61, p = 0.445; Figure S4 B).
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Tumor-immune microenvironment and NRF2 associate with clinical efficacy of PD-1 blockade combined with chemotherapy in lung squamous cell carcinoma.
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