This clinical trial evaluated recombinant human endostatin in breast cancer neoadjuvant chemotherapy. Eighty-seven patients with stage III breast cancer randomly received 4 cycles neoadjuvant of TEC (docetaxel, epirubicin, and cyclophosphamide) or recombinant human endostatin + TEC, followed by surgery. The latter significantly improved the overall survival, suggesting a benefit of adding anti-angiogenesis to standard chemotherapy in the treatment of breast cancer. Background: To explore the potential advantage of preoperative anti-angiogenosis therapy, we implemented a study to evaluate the efficacy of recombinant human endostatin (EN) in combination with neoadjuvant chemotherapy in the treatment of stage III breast cancer. Patients and Methods: Eighty-seven patients were randomized to neoadjuvant TEC (docetaxel, epirubicin, and cyclophosphamide) or to EN+TEC, followed by surgery. The primary endpoint was the objective response rate (ORR). Secondary endpoints included pathologic complete response (pCR), relapse-free survival (RFS), overall survival (OS), and safety. Results: Patients receiving EN+TEC achieved significantly higher ORR (81.82%; 36/44) compared with those receiving TEC (58.14%; 25/43; P=0.016). There was a non-significant trend of increased pCR with EN treatment (15.91% vs. 6.98%). The median follow-up was 54 months and revealed a significantly higher RFS with EN+TEC (median, 67.3 months; 95% confidence interval [CI], 61.0-73.7 months), compared with TEC (median, 55.0 months; 95% CI, 48.3-61.7 months; P =0.014). EN+TEC also significantly improved OS (74.2 months; 95% CI, 68.9-79.6 months), compared with TEC (59.1 months; 95% CI, 52.0-66.1 months; P =0 .006). The 3- and 5-year OS rates are estimated to be 88.5% and 82.8% with EN+TEC and 76.7% and 54.4% with TEC, respectively. Cox proportional regression analyses showed that EN+TEC was associated with improved OS (hazard ratio, 0.377; 95% CI, 0.418-0.959; P =0 .041). There was no significant difference in adverse events between EN+TEC and TEC. Conclusion: The combination of EN+TEC neoadjuvant chemotherapy significantly improved the ORR and OS, suggesting a benefit of adding anti-angiogenesis to standard chemotherapy in the treatment of locally advanced breast cancer. (C) 2020 Elsevier Inc. All rights reserved.
第一作者机构:[1]Hebei Med Univ, Res Ctr, Hosp 4, Shijiazhuang, Hebei, Peoples R China
通讯作者:
通讯机构:[3]Hebei Med Univ, Breast Ctr, Hosp 4, 12 Jiankang Rd, Shijiazhuang 050011, Hebei, Peoples R China[*1]Breast Center, Fourth Hospital of Hebei Medical University, 12 Jiankang Rd, Shijiazhuang, Hebei, China 050011
推荐引用方式(GB/T 7714):
Zhang Xiangmei,Zhang Zhenzhen,Cao Miao,et al.A Randomized Parallel Controlled Phase II Trial of Recombinant Human Endostatin Added to Neoadjuvant Chemotherapy for Stage III Breast Cancer[J].CLINICAL BREAST CANCER.2020,20(4):291-+.doi:10.1016/j.clbc.2020.04.009.
APA:
Zhang, Xiangmei,Zhang, Zhenzhen,Cao, Miao,Liu, Beichen,Mori, Motomi...&Liu, Yunjiang.(2020).A Randomized Parallel Controlled Phase II Trial of Recombinant Human Endostatin Added to Neoadjuvant Chemotherapy for Stage III Breast Cancer.CLINICAL BREAST CANCER,20,(4)
MLA:
Zhang, Xiangmei,et al."A Randomized Parallel Controlled Phase II Trial of Recombinant Human Endostatin Added to Neoadjuvant Chemotherapy for Stage III Breast Cancer".CLINICAL BREAST CANCER 20..4(2020):291-+