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. 2018 Dec 27:11:29-42.
doi: 10.2147/BCTT.S179750. eCollection 2019.

Primary systemic therapy in HER2-positive operable breast cancer using trastuzumab and chemotherapy: efficacy data, cardiotoxicity and long-term follow-up in 142 patients diagnosed from 2005 to 2016 at a single institution

Affiliations

Primary systemic therapy in HER2-positive operable breast cancer using trastuzumab and chemotherapy: efficacy data, cardiotoxicity and long-term follow-up in 142 patients diagnosed from 2005 to 2016 at a single institution

Silvia Antolín et al. Breast Cancer (Dove Med Press). .

Abstract

Objective: The aim of this study was to evaluate the efficacy, cardiotoxicity profile and long-term benefits of neoadjuvant therapy in human epidermal growth factor receptor 2-positive operable breast cancer patients.

Patients and methods: A total of 142 patients diagnosed from 2005 to 2016 were included in the study. The treatment consisted of a sequential regimen of taxanes and anthracyclines plus trastuzumab. The clinical and pathological responses were evaluated and correlated with clinical and biological factors. The cardiotoxicity profile and long-term benefits were analyzed.

Results: The median age was 49 years, and 4%, 69% and 27% of patients had stage I, II and III breast cancer, respectively, while 10% had inflammatory breast cancer at diagnosis. Hormone receptor (HR) status was negative in 43%, and 62% had grade III breast cancer. The clinical complete response rate was 49% and 63% as assessed using ultrasound and magnetic resonance imaging, respectively, and this allowed a high rate of conservative surgery (66%). The pathological complete response (pCR) rate was 52%, and it was higher in HR-negative (64%) patients than in HR-positive (41%) patients and in grade III breast cancer (53%) patients than in grade I-II breast cancer (45%) patients. Patients who achieved pCR had longer disease-free survival and a trend toward improved overall survival. A total of 2% of patients showed a 10% decrease in left ventricular ejection fraction to <50% during treatment. All patients except one recovered after discontinuation of trastuzumab.

Conclusion: A sequential regimen of taxanes and anthracyclines plus trastuzumab was effective, with high pCR rates and long-term benefit, and had a very good cardiotoxicity profile.

Keywords: HER2-positive breast cancer; cardiotoxicity; neoadjuvant therapy; pathological complete response; survival.

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Conflict of interest statement

Disclosure The authors report no conflicts of interest in this work.

Figures

Figure 1
Figure 1
Types of chemotherapy. Notes: *Chemotherapy doses. Paclitaxel: 80 mg/m2, weekly ×12 doses. FEC: 5-fluorouracil: 600 mg/m2/epirubicin: 75 mg/m2/cyclophosphamide: 600 mg/m2 every 3 weeks × four cycles. Myocet: 60 mg/m2/cyclophosphamide: 600 mg/m2/every 3 weeks × four cycles. T: 8 mg/kg IV loading dose followed by 6 mg/kg IV every 3 weeks (a total of 12 months, including in the neoadjuvant and adjuvant setting). Abbreviations: FEC, 5-fluorouracil–epirubicin–cyclophosphamide; IV, intravenous; T, trastuzumab.
Figure 2
Figure 2
DFS assessed using the Kaplan–Meier method. Abbreviation: DFS, disease-free survival.
Figure 3
Figure 3
OS assessed using the Kaplan–Meier method. Abbreviation: OS, overall survival.
Figure 4
Figure 4
DFS based on pCR. Abbreviations: DFS, disease-free survival; pCR, pathological complete response.
Figure 5
Figure 5
OS based on pCR. Abbreviations: OS, overall survival; pCR, pathological complete response.
Figure 6
Figure 6
Basal LVEF at the end of chemotherapy and follow-up. Abbreviation: LVEF, left ventricular ejection fraction.

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