A Phase II Multi-Center Study of Triple Therapy with Paclitaxel, S-1 and Cisplatin in Patients with Advanced Gastric Cancer

被引:18
作者
Iwase, H. [1 ]
Shimada, M. [1 ]
Tsuzuki, T. [1 ]
Ina, K. [2 ]
Sugihara, M. [3 ]
Haruta, J. [4 ]
Shinoda, M. [5 ]
Kumada, T. [6 ]
Goto, H. [7 ]
机构
[1] Nagoya Med Ctr, Nagoya, Aichi, Japan
[2] Nagoya Mem Hosp, Nagoya, Aichi, Japan
[3] Meitetsu Hosp, Nagoya, Aichi, Japan
[4] Japan Red Cross Nagoya First Hosp, Nagoya, Aichi, Japan
[5] Toyota Mem Hosp, Toyota, Japan
[6] Ogaki Municipal Hosp, Ogaki, Japan
[7] Nagoya Univ, Sch Med, Nagoya, Aichi 466, Japan
关键词
Gastric cancer; Combination therapy; Paclitaxel; S-1; Cisplatin; Phase II; CLINICAL-ONCOLOGY-GROUP; PLUS CISPLATIN; 5-FLUOROURACIL; COMBINATION; TRIAL; INFUSION; FLUOROURACIL; CHEMOTHERAPY; METHOTREXATE; DOXORUBICIN;
D O I
10.1159/000328746
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: To carry out a phase II multi-center study on the efficacy and safety of triple combination therapy with paclitaxel, S-1, and cisplatin in patients with unresectable/ metastatic gastric cancer. Methods: A total of 63 patients from 8 institutions were included in this study. Paclitaxel (160 mg/m(2)) was administered by infusion for 3 h on the first day. S-1 (70 mg/m(2)/day) was administered orally for 14 consecutive days from the first day. Cisplatin (60 mg/m(2)) was administered intravenously over 24 h on day 14 of every 28-day cycle. Results: All 63 patients were assessed for clinical efficacy and safety. A total of 259 cycles of treatment were administered (median 4, range 1-10). Grade 3-4 toxicities included neutropenia in 30.2%, thrombocytopenia in 12.7%, and anemia in 11.1%. There was no grade 3-4 non-hematological toxicity or treatment-related death. Complete response was observed in 6 patients and partial response in 34 patients. The overall response rate was 63.5%. The median progression-free survival and response duration were 8.0 and 8.8 months, respectively, and median survival time was 15 months. Conclusions: Triple combination therapy with paclitaxel, S-1, and cisplatin showed promising safety and efficacy profiles with the potential to become a standard regimen for unresectable/metastatic gastric cancer. Copyright (C) 2011 S. Karger AG, Basel
引用
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页码:76 / 83
页数:8
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