TY - JOUR
T1 - Neoadjuvant chemotherapy in triple-negative breast cancer: A multicentric retrospective observational study in real-life setting
AU - Gamucci, Teresa
AU - Pizzuti, Laura
AU - Sperduti, Isabella
AU - Mentuccia, Lucia
AU - Vaccaro, Angela
AU - Moscetti, Luca
AU - Marchetti, Paolo
AU - Carbognin, Luisa
AU - Michelotti, Andrea
AU - Iezzi, Laura
AU - Cassano, Alessandra
AU - Grassadonia, Antonino
AU - Astone, Antonio
AU - Botticelli, Andrea
AU - Magnolfi, Emanuela
AU - Di Lauro, Luigi
AU - Sergi, Domenico
AU - Fuso, Paola
AU - Tinari, Nicola
AU - Barba, Maddalena
AU - Maugeri-Saccà, Marcello
AU - Landucci, Elisabetta
AU - Conti, Francesca
AU - Sanguineti, Giuseppe
AU - De Tursi, Michele
AU - Iafrate, Gianni
AU - Giordano, Antonio
AU - Giordano, Alessandro
AU - Ciliberto, Gennaro
AU - Natoli, Clara
AU - Vici, Patrizia
PY - 2018
Y1 - 2018
N2 - We aimed to assess the efficacy of neoadjuvant chemotherapy (NACT) in a cohort of 213 triple-negative breast cancer (TNBC) patients treated in real-world practice at eight Italian cancer centers. We computed descriptive statistics for all the variable of interest. Factors testing significant in univariate analysis were included in multivariate models. Survival data were compared by Kaplan–Meier curves and log-rank test. The median follow-up was 45 months. We observed 60 (28.2%) pathological complete response (pCR). The sequential anthracyclines-taxanes-based regimens produced the highest rate of pCR (42.6%), followed by concomitant anthracycline-taxane (24.2%), and other regimens (15.6%) (p = 0.008). When analyzing the role of baseline Ki-67, a 50% cut-off was the optimal threshold value for pCR prediction (p = 0.0005). The 5-year disease-free survival (DFS) was 57.3% and the 5-year overall survival (OS) was 70.8%. In patients not achieving pCR, the optimal Ki-67 variation between biopsy and surgical specimen with prognostic relevance on long-term outcomes was 13% (p = 0.04). Patients with a Ki-67 reduction (rKi-67)<13% had worse outcomes compared to those who experienced pCR or a rKi-67≥13%. The number of NACT cycles also affected long-term outcomes (5-year DFS 65.7% vs 51.6% in patients having received >6 cycles compared with their counterparts, p = 0.02). In multivariate analysis, node status, grading, and bio-pathological treatment response (including pCR and rKi-67) impacted DFS and OS. Our results confirmed the advantage conferred by more than 6 cycles of a sequential antracycline-taxane-based NACT. Higher baseline Ki-67 values shows greater predictive significance on pathogical response, while the rKi-67 plays a prognostic role on long-term outcomes.
AB - We aimed to assess the efficacy of neoadjuvant chemotherapy (NACT) in a cohort of 213 triple-negative breast cancer (TNBC) patients treated in real-world practice at eight Italian cancer centers. We computed descriptive statistics for all the variable of interest. Factors testing significant in univariate analysis were included in multivariate models. Survival data were compared by Kaplan–Meier curves and log-rank test. The median follow-up was 45 months. We observed 60 (28.2%) pathological complete response (pCR). The sequential anthracyclines-taxanes-based regimens produced the highest rate of pCR (42.6%), followed by concomitant anthracycline-taxane (24.2%), and other regimens (15.6%) (p = 0.008). When analyzing the role of baseline Ki-67, a 50% cut-off was the optimal threshold value for pCR prediction (p = 0.0005). The 5-year disease-free survival (DFS) was 57.3% and the 5-year overall survival (OS) was 70.8%. In patients not achieving pCR, the optimal Ki-67 variation between biopsy and surgical specimen with prognostic relevance on long-term outcomes was 13% (p = 0.04). Patients with a Ki-67 reduction (rKi-67)<13% had worse outcomes compared to those who experienced pCR or a rKi-67≥13%. The number of NACT cycles also affected long-term outcomes (5-year DFS 65.7% vs 51.6% in patients having received >6 cycles compared with their counterparts, p = 0.02). In multivariate analysis, node status, grading, and bio-pathological treatment response (including pCR and rKi-67) impacted DFS and OS. Our results confirmed the advantage conferred by more than 6 cycles of a sequential antracycline-taxane-based NACT. Higher baseline Ki-67 values shows greater predictive significance on pathogical response, while the rKi-67 plays a prognostic role on long-term outcomes.
KW - long-term outcomes
KW - neoadjuvant chemotherapy
KW - pathological complete response
KW - rKi-67
KW - triple-negative breast cancer
KW - long-term outcomes
KW - neoadjuvant chemotherapy
KW - pathological complete response
KW - rKi-67
KW - triple-negative breast cancer
UR - http://hdl.handle.net/10807/170020
U2 - 10.1002/jcp.26103
DO - 10.1002/jcp.26103
M3 - Article
SN - 0021-9541
VL - 233
SP - 2313
EP - 2323
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
ER -