Recognizing that cancer immunogenicity stems largely from variant peptides, 15 we predicted neo-antigens for each sample, which similarly showed a trend supporting the clinical benefit of SHR-1701.
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Addition of SHR-1701 to first-line capecitabine and oxaliplatin (XELOX) plus bevacizumab for unresectable metastatic colorectal cancer.
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While the PR group exhibited higher tumor mutational burden (TMB), the difference did not reach statistical significance, likely due to the limited sample size (Fig. 4f ).