Feasibility of AC/EC Followed by Weekly Paclitaxel in Node-positive Breast Cancer in Japan

被引:0
|
作者
Ishikawa, Takashi [1 ]
Shimizu, Satoru [2 ]
Katayama, Kiyofumi [3 ]
Chishima, Takashi [4 ]
Hamaguchi, Yohei [5 ]
Doi, Takako [6 ]
Tanabe, Mikiko [6 ]
Kasahara, Akio [7 ]
Yamaguchi, Naotaka
Narui, Kazutaka
Ohta, Ikuko
Matsumoto, Chizuru
Shimizu, Daisuke
Kito, Ayako
Suda, Takashi [8 ]
Inaba, Masaaki [9 ]
Asaga, Taro [9 ]
Momiyama, Nobuyoshi [4 ]
Ichikawa, Yasushi [4 ]
Yoshimoto, Masataka [10 ]
Morita, Satoshi [11 ]
Shimada, Hiroshi [4 ]
机构
[1] Yokohama City Univ, Med Ctr, Dept Breast & Thyroid Surg, Minami Ku, Yokohama, Kanagawa 2320024, Japan
[2] Mishuku Hosp, Dept Surg, Tokyo, Japan
[3] Hiratsuka Kyosai Hosp, Dept Surg, Kanagawa, Japan
[4] Yokohama City Univ, Grad Sch Med, Dept Surg Gastroenterol, Yokohama, Kanagawa 232, Japan
[5] Yokosuka Kyosai Hosp, Dept Surg, Yokosuka, Kanagawa, Japan
[6] Natl Hosp Org, Yokohama Med Ctr, Dept Surg, Kanagawa, Japan
[7] Kanagawa Ashigarakami Hosp, Dept Surg, Kanagawa, Japan
[8] Saiseikai Nanbu Hosp, Dept Surg, Yokohama, Kanagawa, Japan
[9] Kanagawa Canc Ctr, Dept Breast & Thyroid Surg, Kanagawa, Japan
[10] Int Univ Hlth & Welf, Mita Hosp, Breast Ctr, Minato Ku, Tokyo, Japan
[11] Yokohama City Univ, Med Ctr, Dept Biostat, Yokohama, Kanagawa 2320024, Japan
关键词
Breast cancer; adjuvant chemotherapy; feasibility; adriamycin; epirubicin; paclitaxel; SURGICAL ADJUVANT BREAST; RANDOMIZED-TRIAL; DOSE INTENSITY; STAGE-II; CHEMOTHERAPY; CYCLOPHOSPHAMIDE; FLUOROURACIL; METHOTREXATE; EPIRUBICIN; TAMOXIFEN;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The feasibility and efficacy of adriamycin or epirubicin in combination with cyclophosphamide followed by weekly paclitaxel (AC/EC-weekly PAC) as adjuvant chemotherapy for breast cancer was investigated. Patients and Methods: Node-positive breast cancer was treated with AC/EC-weekly PAC, namely AC at 60/600 mg/m(2) or EC at 90/600 mg/m(2) x 4 at three-week intervals, followed by weekly PAC (80 mg/m(2)) x 12, namely four cycles of single weekly administration for three weeks followed by a one-week rest (3x4 PAC) or single weekly administration for 12 consecutive weeks (12 PAC). Results: One hundred and three of 109 consecutive patients enrolled were analyzed, of whom 96 (93.2%) completed the regimen. Grade 314 neutropenia occurred in 52.4% receiving AC/EC, and 10.9% of 55 receiving 12 PAC but only 2.1% of 48 receiving 3x4 PAC. Neuropathy disorders occurred in more than half receiving PAC, which did not improve after one-week rest in 3x4 PAC. Conclusion: AC/EC-weekly PAC is feasible and without serious complications.
引用
收藏
页码:1515 / 1520
页数:6
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