Multicenter phase II trial of combination chemotherapy with weekly paclitaxel and 5-fluorouracil for the treatment of advanced or recurrent gastric carcinoma

被引:27
作者
Ninomiya, M.
Kondo, K.
Matsuo, K.
Hirabayashi, N.
Kojima, H.
Kobayashi, M.
Kawamura, S.
Ando, T.
Musha, N.
Konno, H.
Nagata, N.
Usuki, H.
Miyashita, Y.
Oba, K.
Morita, S.
Sakamoto, J.
机构
[1] Hiroshima City Hosp, Dept Surg, Hiroshima, Japan
[2] Med Ctr, Natl Hosp Org, Dept Surg, Nagoya, Aichi, Japan
[3] Shimonoseki Municipal Hosp, Dept Surg, Shimonoseki, Yamaguchi, Japan
[4] Hiroshima City Asa Hosp, Dept Surg, Hiroshima, Japan
[5] Aichi Canc Ctr Hosp, Dept Surg Gastroenterol, Nagoya, Aichi 464, Japan
[6] Kochi Univ, Dept Surg, Kochi 780, Japan
[7] Med Ctr, Natl Hosp Org, Dept Surg, Kobe, Hyogo, Japan
[8] Hata Prefectural Hosp, Dept Surg, Sukumo, Japan
[9] Saiseikai Niigata Daini Hosp, Dept Surg, Niigata, Japan
[10] Hamamatsu Univ Sch Med, Dept Surg 2, Hamamatsu, Shizuoka 43131, Japan
[11] Univ Occupat & Environm Hlth, Sch Med, Dept Surg 1, Kitakyushu, Fukuoka 807, Japan
[12] Kagawa Univ Hosp, Dept Surg 1, Kagawa, Japan
[13] Kyoto Univ, Dept Epidemiol & Clin Res Informat Management, Kyoto, Japan
[14] Nagoya Univ, Grad Sch Med, Young Leaders Program, Nagoya, Aichi, Japan
关键词
advanced gastric cancer; clinical triats; paclitaxel; 5-fluorouracil; multicenter clinical trial;
D O I
10.1179/joc.2007.19.4.444
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study was to investigate the efficacy and safety of combination chemotherapy with weekly paclitaxel and 5-fluorouracil (5-FU) as first-line treatment in patients with advanced or recurrent gastric carcinoma. A total of 65 patients were treated with the following regimen, administered every 28 days; 5-FU 600 mg/m(2) by 24-hour continuous infusion from days 1 through 5, and weekly paclitaxel 80 mg/m(2) by 3-hour intravenous infusion on days 8, 14, and 21. A total of 272 cycles were conducted with a median of 4 (2-13) cycles per case. Out of 57 patients with measurable disease by RECIST criteria, there were 2 complete responses (3.5%), 20 partial responses (35.1%) and 25 cases with stable disease (43.9%). The overall response rate was 38.6% (95%CI: 26.0-51.2%). The median survival time and 1-year survival rates were 329 days and 47.4%, respectively. Both hematologic and non-hematologic toxicities were well tolerated.
引用
收藏
页码:444 / 450
页数:7
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