Neoadjuvant Weekly Paclitaxel with and without Trastuzumab in Locally Advanced or Metastatic Breast Cancer

A phase II clinical trial was conducted to examine the clinical and pathologic efficacy and safety of neoadjuvant paclitaxel with or without trastuzumab in women with advanced or metastatic breast cancer. A total of 49 patients with advanced or metastatic breast cancer (clinical stage IIB -IV) were included. Patients with HER2- negative tumors received weekly paclitaxel 80 mg/m 2 (days 1, 8, 15) followed by a 1-week break for 4 cycles. Patients with HER2-positive tumors received weekly paclitaxel 80 mg/m 2 (days 1, 8, 15) followed by a 1-week break and a trastuzumab 4 mg/kg loading dose, intravenously, followed by 2 mg/kg weekly for 4 cycles. The age of the patients was 51.6±1.6 years (mean±SE) and the size of their tumors was 5.8±0.4 cm (mean±SE). Thirty-two patients had HER2- negative tumors and 17 had HER2-positive tumors. Of 49 patients, 13 (26.5% ) had a clinical complete response and 24 (49.0% ) had a clinical partial response. Five (10.2% ) patients had a pathological complete response (pCR) and three (6.1% ) patients had a near pCR in the breast. A total of eight (16.3% ) patients had a pCR or near pCR in the breast. The pCR or near pCR rate was 3.1% in the HER2- negative group and 41.2% in the HER2-positive group. With a median follow-up of 28 months (range, 1-45), the 3-year overall survival was 88% . Clinical responders showed a significantly better overall survival than non-responders (p<0.01). Pathological responders showed a better overall survival than non-responders. There was no significant difference in overall survival between patients with HER2- positive and -negative tumors. In conclusion, combined neoadjuvant weekly paclitaxel and trastuzumab achieved high clinical and pathological response rates for HER2 - overexpressing breast cancers, despite the omission of an anthracycline.