2 ) did not identify any clinical or pathological subgroup that consistently benefited substantially from anlotinib-based NAT in the tpCR or RCB 0/I rate, despite a numerical trend favoring node-negative (N0) patients.
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Anlotinib combined with neoadjuvant chemotherapy for HR+/HER2- breast cancer (ACNTBC): a prospective, single-arm, single-center phase II clinical study with real-world validation.
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Consequently, despite the numerical difference, the 2-year EFS rates did not reach statistical significance compared to the IPTW-weighted control group.