Abstract

PurposeTo assess the predictive role of pretreatment ki67 and Ki67 changes in breast cancer (BC) patients treated with neoadjuvant chemotherapy (NAC) in various molecular subtypes.Methods1010 BC patients who had undergone anthracycline and taxane-based NAC from January 2012 to July 2017 were retrospectively analyzed. Clinical and pathological parameters of the patients were retrieved and the predictive factors for NAC response were evaluated.Results705 patients showed clinical response (cRes), and 131 patients acquired pathologic complete response (pCR). Patients with higher pretreatment Ki67 (≥ 14%), tumor size ≥ 4 cm, and positive clinical nodal had better clinical therapy response, while patients with negative ER and PR, higher pretreatment Ki67 (≥ 14%), and tumor size < 4 cm were more probable to attain pCR. The pretreatment Ki67 could be used as a predictor of NAC only in luminal subtypes, and 25.5% were identified as an ideal cut-off point to differentiate the cRes from non-cRes cases. Although a decrease in Ki67 had been found in almost all molecular subtypes after NAC, no statistically significant differences were found in the decrease of Ki67 were validated between the cRes and non-cRes group in HER2-rich and triple-negative subtypes (P = 0.488 and P = 0.111, respectively).ConclusionsThe best cut-off for pretreatment Ki67 in predicting the connection with the tumor size lessening was 25.5% in luminal subtype. Aggressive adjuvant systemic treatments should be considered for patients with HER2-rich and triple-negative subtype who exhibit tumor shrinkage in NAC but still have high levels of Ki67.

Highlights

  • Neoadjuvant chemotherapy (NAC) is a standard treatment for advanced breast cancer (BC) patients with the aim to decrease the extent of surgery [1]

  • One hundred and thirty-one patients (13.0%) achieved pathologic complete response (pCR), and 574 patients (56.8%) showed clinical response to NAC based on the Response Evaluation Criteria in Solid Tumors (RECIST) criteria, while 305 patients (30.4%) showed no response, including 290 of cSD (28.7%) and 15 of cPD (1.5%)

  • We explored the association between tumor size reduction and the decrease of Ki67 in different molecular subtypes (Fig. 4)

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Summary

Introduction

Neoadjuvant chemotherapy (NAC) is a standard treatment for advanced breast cancer (BC) patients with the aim to decrease the extent of surgery [1]. Many studies have revealed effective predictors of the response to NAC with different molecular subtypes [4,5,6], but some of these conclusions remain controversial

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