A Randomized Phase II Study of Eribulin/Cyclophosphamide or Docetaxel/Cyclophosphamide as Neoadjuvant Therapy in Operable HER2-negative Breast Cancer

The present phase II study compared the combination of eribulin plus cyclophosphamide (ErC) to docetaxel plus cyclophosphamide (TC) as neoadjuvant therapy for HER2 - breast cancer patients. Patients received either eribulin 1.4 mg/m(2) on days 1 and 8 plus cyclophosphamide 600 mg/m(2) on day 1 or docetaxel 75 mg/m(2) plus cyclophosphamide 600 mg/m 2 on day 1 for 6 cycles before surgery. Neoadjuvant ErC showed no greater efficacy than TC. Background: Eribulin mesylate is a non-taxane microtubule inhibitor effective in the treatment of metastatic breast cancer refractory to anthracyclines and taxanes. In preclinical studies, additional mechanisms of eribulin included reversal of epithelial mesenchymal transition and tumor vascular remodeling. The present study compared the safety and efficacy of eribulin plus cyclophosphamide (ErC) to docetaxel plus cyclophosphamide (TC) as neoadjuvant therapy for operable HER2 breast cancer. Patients and Methods: Women with invasive HER2 breast adenocarcinoma with no distant metastases were eligible. After a 10-patient safety lead-in, the patients were randomized 2:1 to receive either ErC (eribulin 1.4 mg/m(2) on days 1 and 8 plus cyclophosphamide 600 mg/m(2) on day 1) or TC (docetaxel 75 mg/m(2) plus cyclophosphamide 600 mg/m(2) on day 1) administered every 21 days for 6 cycles, followed by surgery. The pathologic complete response (pCR) rate was the primary endpoint. Tumor samples collected at baseline and at surgery were assayed for select epithelial mesenchymal transition and vascular density markers: E-cadherin, vimentin, and CD31 expression. Results: A total of 76 patients were enrolled. Of the 76 patients, 10 received ErC in the lead-in phase and 66 were randomized to ErC (n - 44) or TC (n- 22). The pCR rates with Ere and TC were 13% and 9%, respectively. Both regimens produced frequent neutropenia and peripheral neuropathy. Both regimens increased vascular density as measured by CD31 staining. Conclusion: The neoadjuvant regimens of ErC and TC resulted in relatively low pCR rates in this patient population. No unexpected toxicities were observed. Our results also provided no suggestion that ErC is a neoadjuvant treatment with greater efficacy than that of standard regimens. (C) 2018 Elsevier Inc. All rights reserved.