We aimed to investigate the correlation between neutrophil-to-lymphocyte ratio (NLR) and pathologic complete response (pCR) and survival outcomes in human epidermal growth factor receptor 2 (HER2)-negative breast cancer patients who received neoadjuvant chemotherapy. The baseline NLR was evaluated in non-metastatic, HER2-negative breast cancer patients who received neoadjuvant chemotherapy. Baseline NLR was calculated as absolute neutrophil per lymphocyte count from pre-treatment blood samples. Any value ≥ 2.74 was considered to be a high NLR. In the 1,097 patients studied, 272 (24.4%) had high NLR and 825 (75.6%) had low NLR. The high NLR was an independent factor for pCR (OR 0.595; 95% CIs 0.398-0.890; P = 0.011). Furthermore, high NLR was a significant independent parameter affecting DFS (HR 2.298; 95% CIs 1.691-3.124; P < 0.001) and OS (HR 1.905; 95% CIs 1.167-3.108; P = 0.010). Regardless of the baseline NLR, survival outcomes were excellent in patients who achieved pCR, but high NLR was associated with worse survival for patients with residual invasive disease. Our study showed that NLR was predictive for treatment response and a prognostic factor in patients with HER2-negative breast cancer who received neoadjuvant chemotherapy. Moreover, we identified that high NLR was associated with poor survival outcomes in patients who did not achieve pCR. Neoadjuvant chemotherapy before definitive cancer surgery is increasingly being accepted as a treatment for breast cancer 1. Neoadjuvant chemotherapy has survival outcomes equivalent to those of adjuvant chemotherapy 2,3 , but also has the following advantages: it can increase the rate of breast-conserving surgery by reducing the size and extent of locally advanced tumors, control occult micro-metastasis, and estimate sensitivity to treatment regimen 4,5. Besides, it encourages the development and approval of new agents by allowing rapid assessment of drug efficacy in neoadjuvant trials 6. To date, pathologic complete response (pCR) following the reception of neoadjuvant chemotherapy has been suggested as a surrogate marker for a long-term clinical benefit 7-9. In particular, patients with HER2-positive breast cancer or triple-negative breast cancer (TNBC) who achieved pCR show improved survival than those with residual invasive disease 10 .