Abstract

Uncertainty exists around the need to include an anthracycline if taxane-based adjuvant chemotherapy is being used for human epidermal growth factor receptor-2 (HER2) negative and axillary lymph node negative (LNN) breast cancer. We identified all patients who were diagnosed with HER2-negative, LNN breast cancer treated with docetaxel-cyclophosphamide for four cycles (DC4) or an anthracycline-taxane (AT) regimen following surgical resection in Alberta from 2008 through 2012. We used propensity score methods to match each patient treated with AT to up to four patients treated with DC4 on potentially confounding clinicopathologic and treatment variables. We compared the 10-year invasive disease free survival (iDFS), breast cancer specific-survival (BCSS) and overall survival (OS) and assessed the effect of the type of adjuvant chemotherapy on these outcomes using Cox regression. Of the 726 eligible patients, 657 (90.5%) were treated with DC4 and 69 (9.5%) were treated with AT. Matching created a group of 202 women treated with DC4 and eliminated differences in clinicopathologic and treatment factors. There was no statistically significant difference for the treatment effects of matched DC4 patients compared to the AT patients on iDFS (75.7% vs. 76.8%, p = 0.75; hazard ratio (HR) = 1.05, 95% CI = 0.65 to 1.8), BCSS (88.1% vs. 87%, p = 0.8; HR = 0.91, 95% CI = 0.42 to 1.9), or OS (87.1% vs. 86.9%, p= 0.96; HR = 0.98, 95% CI = 0.46 to 2.1). Four cycles of DC as compared with an AT regimen yielded similar 10-year iDFS, BCSS and OS amongst patients with HER2-negative, LNN breast cancer.

Highlights

  • Adjuvant anthracycline-taxane (AT) combinations for human epidermal growth factor receptor-2 (HER2) negative breast cancer have been widely studied and adopted due to improved survival outcomes in comparison to historical anthracycline-only regimens [1,2,3,4].anthracyclines are associated with small increases in the absolute risks for late, irreversible cardiotoxicity, myelodysplastic syndromes and leukemias [5]

  • We examined whether the association of adjuvant chemotherapy (DC4 vs. AT) with 10-year invasive disease free survival (iDFS), breast cancer specific-survival (BCSS), and overall survival (OS) is different by tumour characteristics by testing for interactions between these tumour characteristics and the type of adjuvant chemotherapy (DC4 vs. AT)

  • We identified 726 patients who were diagnosed with lymph node negative (LNN), HER2-negative breast cancer during the period from 1 January 2008 to 31 December 2012 and met our study inclusion criteria

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Summary

Introduction

Adjuvant anthracycline-taxane (AT) combinations for human epidermal growth factor receptor-2 (HER2) negative breast cancer have been widely studied and adopted due to improved survival outcomes in comparison to historical anthracycline-only regimens [1,2,3,4].anthracyclines are associated with small increases in the absolute risks for late, irreversible cardiotoxicity, myelodysplastic syndromes and leukemias [5]. Adjuvant anthracycline-taxane (AT) combinations for human epidermal growth factor receptor-2 (HER2) negative breast cancer have been widely studied and adopted due to improved survival outcomes in comparison to historical anthracycline-only regimens [1,2,3,4]. Docetaxel plus cyclophosphamide for four cycles (DC4) has been compared with the anthracycline-only regimen and doxorubicin plus cyclophosphamide for four cycles (AC4), and demonstrated superior disease-free survival (DFS) and overall survival (OS) [6]. Subsequent trials have attempted to address the effectiveness of six cycles of DC (DC6) compared to the more widely used AT regimens [7,8,9]. In Alberta, DC4 has been used as a standard adjuvant chemotherapy regimen for HER2-negative, lymph node negative (LNN) breast cancer.

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