TY - JOUR
T1 - Response to Neoadjuvant Therapy and Long-Term Survival in Patients With Triple-Negative Breast Cancer
AU - Liedtke, Cornelia
AU - Mazouni, Chafika
AU - Hess, Kenneth R.
AU - André, Fabrice
AU - Tordai, Attila
AU - Mejia, Jaime A.
AU - Symmans, W. Fraser
AU - Gonzalez-Angulo, Ana M.
AU - Hennessy, Bryan
AU - Green, Marjorie
AU - Cristofanilli, Massimo
AU - Hortobagyi, Gabriel N.
AU - Pusztai, Lajos
N1 - Publisher Copyright:
© 2008 by American Society of Clinical Oncology.
PY - 2023/4/1
Y1 - 2023/4/1
N2 - PURPOSETriple-negative breast cancer (TNBC) is defined by the lack of estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER-2) expression. In this study, we compared response to neoadjuvant chemotherapy and survival between patients with TNBC and non-TNBC.PATIENTS AND METHODSAnalysis of a prospectively collected clinical database was performed. We included 1,118 patients who received neoadjuvant chemotherapy at M.D. Anderson Cancer Center for stage I-III breast cancer from 1985 to 2004 and for whom complete receptor information were available. Clinical and pathologic parameters, pathologic complete response rates (pCR), survival measurements, and organ-specific relapse rates were compared between patients with TNBC and non-TNBC.RESULTSTwo hundred fifty-five patients (23%) had TNBC. Patients with TNBC compared with non-TNBC had significantly higher pCR rates (22% v 11%; P =.034), but decreased 3-year progression-free survival rates (P <.0001) and 3-year overall survival (OS) rates (P <.0001). TNBC was associated with increased risk for visceral metastases (P =.0005), lower risk for bone recurrence (P =.027), and shorter postrecurrence survival (P <.0001). Recurrence and death rates were higher for TNBC only in the first 3 years. If pCR was achieved, patients with TNBC and non-TNBC had similar survival (P =.24). In contrast, patients with residual disease (RD) had worse OS if they had TNBC compared with non-TNBC (P <.0001).CONCLUSIONPatients with TNBC have increased pCR rates compared with non-TNBC, and those with pCR have excellent survival. However, patients with RD after neoadjuvant chemotherapy have significantly worse survival if they have TNBC compared with non-TNBC, particularly in the first 3 years.
AB - PURPOSETriple-negative breast cancer (TNBC) is defined by the lack of estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER-2) expression. In this study, we compared response to neoadjuvant chemotherapy and survival between patients with TNBC and non-TNBC.PATIENTS AND METHODSAnalysis of a prospectively collected clinical database was performed. We included 1,118 patients who received neoadjuvant chemotherapy at M.D. Anderson Cancer Center for stage I-III breast cancer from 1985 to 2004 and for whom complete receptor information were available. Clinical and pathologic parameters, pathologic complete response rates (pCR), survival measurements, and organ-specific relapse rates were compared between patients with TNBC and non-TNBC.RESULTSTwo hundred fifty-five patients (23%) had TNBC. Patients with TNBC compared with non-TNBC had significantly higher pCR rates (22% v 11%; P =.034), but decreased 3-year progression-free survival rates (P <.0001) and 3-year overall survival (OS) rates (P <.0001). TNBC was associated with increased risk for visceral metastases (P =.0005), lower risk for bone recurrence (P =.027), and shorter postrecurrence survival (P <.0001). Recurrence and death rates were higher for TNBC only in the first 3 years. If pCR was achieved, patients with TNBC and non-TNBC had similar survival (P =.24). In contrast, patients with residual disease (RD) had worse OS if they had TNBC compared with non-TNBC (P <.0001).CONCLUSIONPatients with TNBC have increased pCR rates compared with non-TNBC, and those with pCR have excellent survival. However, patients with RD after neoadjuvant chemotherapy have significantly worse survival if they have TNBC compared with non-TNBC, particularly in the first 3 years.
UR - http://www.scopus.com/inward/record.url?scp=85151172835&partnerID=8YFLogxK
U2 - 10.1200/JCO.22.02572
DO - 10.1200/JCO.22.02572
M3 - Article
C2 - 36989609
AN - SCOPUS:85151172835
SN - 0732-183X
VL - 41
SP - 1809
EP - 1815
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 10
ER -