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. 2021 May 4:2021:5548252.
doi: 10.1155/2021/5548252. eCollection 2021.

Prognostic Impact of Ki-67 Change in Locally Advanced and Early Breast Cancer after Neoadjuvant Chemotherapy: A Single Institution Experience

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Prognostic Impact of Ki-67 Change in Locally Advanced and Early Breast Cancer after Neoadjuvant Chemotherapy: A Single Institution Experience

Mirco Pistelli et al. J Oncol. .

Abstract

Systemic neoadjuvant chemotherapy (NCT) is a standard treatment for locally advanced breast cancer (LABC) and for selected early breast cancer (EBC). In these settings, the prognostic and predictive role of Ki-67 before and after NCT is unclear. The aim of our study was to investigate the prognostic role of Ki-67 change in patients not achieving pathological complete response (pCR). We retrospectively analyzed data of patients who did not achieve pCR assessing Ki-67 expression pre- and post-NCT. We stratified three groups: high reduction (>20%), low reduction (1-20%), and no reduction in Ki-67. These groups were correlated with clinical and pathological data by χ2 test. We estimated disease-free survival (DFS) and overall survival (OS) using Kaplan-Meier method, and we adopted univariate and multivariate Cox proportional hazard models. We selected 82 patients from a database of 143 patients, excluding those who were metastatic at diagnosis, achieved pCR, or lack data regarding Ki-67. Median age at diagnosis was 54 years (range 30-75); 51 patients were Luminal B, 10 human epidermal growth factor receptor 2 (HER-2) enriched, and 21 triple negative. A significant correlation between high Ki-67 reduction and luminal B HER-2-negative subtype was observed (p = 0,0035). The change in Ki-67 was significantly associated with DFS (p = 0,0596) and OS (p = 0,0120), also at multivariate analysis (p = 0,0256 for DFS; p = 0,0093 for OS). In particular, as compared to patients with low/no reduction of Ki-67, those with high Ki-67 reduction (>20%) after NCT showed better survival (60% vs. 56% vs. 83% after 5 years from diagnosis, respectively; p = 0.01). In conclusion, in our study, Ki-67 change showed a significant prognostic role in breast cancer patients treated with NCT who did not achieve pCR. Crucially, Ki-67 < 20% identifies a high-risk population that may be eligible for clinical trials with novel therapeutic interventions in adjuvant setting.

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Conflict of interest statement

The authors declare that there are no conflicts of interest regarding the publication of this article.

Figures

Figure 1
Figure 1
We identified 143 patients treated with neoadjuvant therapy for breast cancer; 82 patients were eligible for the analysis.
Figure 2
Figure 2
(a) Ki-67 reduction associated with Overall Survival (p=0,0120); (b) Ki-67 reduction associated with Disease-Free Survival (p=0,0596).

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References

    1. Cortazar P., Zhang L., Untch M., et al. Pathological complete response and long-term clinical benefit in breast cancer: the CTNeoBC pooled analysis. The Lancet. 2014;384(9938):164–172. doi: 10.1016/s0140-6736(13)62422-8. - DOI - PubMed
    1. Von Minckwitz G., Untch M., Blohmer J.-U., et al. Definition and impact of pathologic complete response on prognosis after neoadjuvant chemotherapy in various intrinsic breast cancer subtypes. Journal of Clinical Oncology. 2012;30(15):1796–1804. doi: 10.1200/jco.2011.38.8595. - DOI - PubMed
    1. Masuda N., Lee S.-J., Ohtani S., et al. Adjuvant capecitabine for breast cancer after preoperative chemotherapy. New England Journal of Medicine. 2017;376(22):2147–2159. doi: 10.1056/nejmoa1612645. - DOI - PubMed
    1. Von Minckwitz G., Huang C.-S., Mano M. S., et al. Trastuzumab emtansine for residual invasive HER2-positive breast cancer. New England Journal of Medicine. 2019;380(7):617–628. doi: 10.1056/nejmoa1814017. - DOI - PubMed
    1. Nishimura R., Osako T., Okomura Y., Hayashi M., Toyozumi Y., Arimal N. Ki-67 as a prognostic marker according to breast cancer subtype and a predictor of recurrence time in primary breast cancer. Experimental and Therapeutic Medicine. 2010;1(5):747–754. doi: 10.3892/etm.2010.133. - DOI - PMC - PubMed