Comparison of an AC-Taxane Versus AC-Free Regimen and Paclitaxel Versus Docetaxel in Patients With Lymph Node-Positive Breast Cancer: Final Results of the National Surgical Adjuvant Study of Breast Cancer O 2 Trial, a Randomized Comparative Phase 3 Study

被引:28
|
作者
Watanabe, Toru [1 ]
Kuranami, Masaru [2 ]
Inoue, Kenichi [3 ]
Masuda, Norikazu [4 ]
Aogi, Kenjiro [5 ]
Ohno, Shinji [6 ]
Iwata, Hiroji [7 ]
Mukai, Hirofumi [8 ]
Uemura, Yukari [9 ]
Ohashi, Yasuo [10 ]
机构
[1] Hamamatsu Oncol Ctr, Dept Med Oncol, 3-6-13 Chuo, Hamamatsu, Shizuoka 4300929, Japan
[2] Yamato Municipal Hosp, Dept Surg, Yamato, Japan
[3] Saitama Canc Ctr, Breast Oncol, Kita Adachi, Japan
[4] Natl Hosp Org, Osaka Natl Hosp, Dept Surg, Div Breast Surg, Osaka, Japan
[5] Natl Hosp Org, Shikoku Canc Ctr, Dept Breast Oncol, Matsuyama, Ehime, Japan
[6] Canc Inst tute Hosp Japanese Fdn Canc Res, Breast Oncol Ctr, Tokyo, Japan
[7] Aichi Canc Ctr Hosp, Dept Breast Oncol, Nagoya, Aichi, Japan
[8] Natl Canc Ctr Hosp East, Dept Oncol & Hematol, Kashiwa, Chiba, Japan
[9] Tokyo Univ Hosp, Clin Res Support Ctr CresCent, Tokyo, Japan
[10] Chuo Univ, Dept Integrated Sci & Engn Sustainable Soc, Tokyo 112, Japan
关键词
adjuvant therapy; docetaxel; doxorubicin and cyclophosphamide (AC); taxane; paclitaxel; randomized phase 3; CHEMOTHERAPY; CYCLOPHOSPHAMIDE; LEUKEMIA;
D O I
10.1002/cncr.30421
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: In postoperative patients with breast cancer, the combination of an anthracycline and cyclophosphamide (AC) followed by a taxane is a standard regimen. In the current study, the authors examined whether AC could be safely omitted, and compared the effectiveness of paclitaxel versus docetaxel.METHODS: Female postoperative patients with axillary lymph node-positive breast cancer were eligible for enrollment in this phase 3, open-label, randomized controlled trial at 84 centers in Japan. Patients were randomized to 4 cycles of doxorubicin at a dose of 60mg/m(2) and cyclophosphamide at a dose of 600mg/m(2) (AC) followed by 4 cycles of paclitaxel at a dose of 175mg/m(2) (ACpT) or AC followed by 4 cycles of docetaxel at a dose of 75mg/m(2) (ACdT), or 8 cycles of paclitaxel (PTx) or docetaxel (DTx) every 3 weeks. The primary endpoint was disease-free survival (DFS). Secondary endpoints included overall survival adverse events. The authors adopted a 232 factorial design to examine the AC containing-regimens (ACpT and ACdT) versus the AC free-regimens (PTx and DTx), and the paclitaxel-containing regimens (ACpT and PTx) versus the docetaxel-containing regimens (ACdT and DTx). RESULTS: Of 1060 patients, 1049 were treated and included in the intention-to-treat population. The DFS results did not demonstrate noninferiority between the AC-containing and the AC-free regimens (hazard ratio [HR], 1.19; 95% confidence interval [95% CI], 0.982-1.448 [Pnoninferiority5.30]). Better outcomes were noted in patients treated with the docetaxel-containing regimens compared with the paclitaxel-containing regimens with respect to DFS (HR, 0.72; 95% CI, 0.589-0.875 [P5.0008]) and overall survival (HR, 0.75; 95% CI, 0.574-0.980 [P5.035]). Neutropenia, nausea, and vomiting were found to occur more often in the AC-containing arms, whereas the incidence of edema was greater in the docetaxel-containing treatment arms. CONCLUSIONS: Noninferiority in DFS was not demonstrated between the AC-containing and AC-free regimens. Compared with a similar regimen of paclitaxel, docetaxel appeared to increase the DFS. Cancer 2017; 123: 759-68. VC 2017 American Cancer Society.
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收藏
页码:759 / 768
页数:10
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