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A Randomized Parallel Controlled Phase II Trial of Recombinant Human Endostatin Added to Neoadjuvant Chemotherapy for Stage III Breast Cancer

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机构: [1]Hebei Med Univ, Res Ctr, Hosp 4, Shijiazhuang, Hebei, Peoples R China [2]Oregon Hlth & Sci Univ, OHSU PSU Sch Publ Hlth, Portland, OR 97201 USA [3]Hebei Med Univ, Breast Ctr, Hosp 4, 12 Jiankang Rd, Shijiazhuang 050011, Hebei, Peoples R China [4]Hebei Med Univ, Dept Hematol, Hosp 4, Shijiazhuang, Hebei, Peoples R China [5]St Jude Childrens Res Hosp, Dept Biostat, 332 N Lauderdale St, Memphis, TN 38105 USA [6]Oregon Hlth & Sci Univ, Knight Canc Inst, Div Hematol & Med Oncol, Portland, OR 97201 USA [7]Oregon Hlth & Sci Univ, Div Hematol Oncol, Knight Canc Inst, Portland, OR 97201 USA [8]Hebei Med Univ, Dept Pathol, Hosp 4, Shijiazhuang, Hebei, Peoples R China
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关键词: Breast cancer Neoadjuvant therapy Objective response rate Overall survival Recombinant human endostatin

摘要:
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.

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出版当年[2020]版:
大类 | 3 区 医学
小类 | 4 区 肿瘤学
最新[2025]版:
大类 | 3 区 医学
小类 | 4 区 肿瘤学
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出版当年[2020]版:
Q3 ONCOLOGY
最新[2023]版:
Q2 ONCOLOGY

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第一作者机构: [1]Hebei Med Univ, Res Ctr, Hosp 4, Shijiazhuang, Hebei, Peoples R China
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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
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