Bevacizumab as First-line Treatment for HER2-negative Advanced Breast Cancer: Paclitaxel plus Bevacizumab Versus Other Chemotherapy

被引:4
|
作者
Nakamoto, Shogo [1 ]
Watanabe, Junichiro [1 ]
Ohtani, Shoichiro [2 ]
Morita, Satoshi [3 ]
Ikeda, Masahiko [4 ]
机构
[1] Shizuoka Canc Ctr, Dept Breast Oncol, 1007 Shimonagakubo,Nagaizumi Cho, Shizuoka, Shizuoka, Japan
[2] Hiroshima City Hiroshima Citizens Hosp, Dept Breast Surg, Hiroshima, Japan
[3] Kyoto Univ, Dept Biomed Stat & Bioinformat, Grad Sch Med, Kyoto, Japan
[4] Fukuyama City Hosp, Dept Breast & Thyroid Gland Surg, Fukuyama, Hiroshima, Japan
来源
IN VIVO | 2020年 / 34卷 / 03期
关键词
Advanced breast cancer; bevacizumab; HER2-negative; propensity score matching; real world; PHASE-III; NON-INFERIORITY; GROWTH-FACTOR; OPEN-LABEL; THERAPY; CAPECITABINE; COMBINATION; BIOMARKERS; DOCETAXEL; SURVIVAL;
D O I
10.21873/invivo.11917
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: The efficacy of paclitaxel and bevacizumab (PB) compared with other chemotherapies in patients with human epidermal growth factor receptor 2-negative (HER2) advanced breast cancer is unclear. Patients and Methods: We retrospectively investigated 301 patients with HER2(-) ABC who received first-line chemotherapy from January 2011 to December 2016. Results: We included 114 patients who received PB and 187 patients who received other chemotherapies. After propensity score matching, the PB group showed a significantly superior overall response rate (77.8% vs. 38.9%, p<0.0001) and median time to treatment failure (73 vs. 5.9 months, p=0.035). In subgroup analyses, PB improved the median overall survival of patients with pleural lesions or pulmonary lymphangiopathy (not reached vs. 18.9 months, p=0.037), and of patients with three or more metastatic sites without liver metastases, (48.0 vs. 27.3 months, p=0.015). Conclusion: Compared with conventional chemotherapy, PB improved the overall response rate and time to treatment failure in patients with HER2(-) advanced breast cancer and improved overall survival in some patient subgroups.
引用
收藏
页码:1377 / 1386
页数:10
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