Gemcitabine monotherapy in patients with locally advanced or metastatic pancreatic cancer: a prospective observational study

被引:8
作者
Karasek, P
Skacel, T
Kocakova, I
Bednarik, O
Petruzelka, L
Melichar, B
Bustova, I
Spurny, V
Trason, T
机构
[1] Masaryk Mem Canc Inst Brno, Dept Oncol, Brno 65653, Czech Republic
[2] Gen Teaching Hosp Prague, Dept Oncol, Prague, Czech Republic
[3] Univ Hosp Hradec Kralove, Dept Radiotherapy & Oncol, Hradec Kralove, Czech Republic
[4] Gen Hosp, Dept Radiotherapy & Oncol, Ceske Budejovice, Czech Republic
[5] St Anns Univ Hosp Brno, Dept Oncol, Brno, Czech Republic
关键词
gemcitabine; monotherapy; observational study; pancreatic cancer;
D O I
10.1517/14656566.4.4.581
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Pancreatic cancer has one of the worst prognosis of any malignant disease. Systemic therapy is often administered because the disease is usually detected at advanced stages. Gemcitabine (Gemzar(TM), Eli Lilly & Co.) has proven activity in the treatment of pancreatic cancer. Gemcitabine 1000 mg/m(2) was given on days 1, 8 and 15, every 4 weeks. A total of 100 chemonaive patients with locally advanced or metastatic pancreatic cancer were enrolled; 32 and 68% had stage III and IV disease, respectively. The average number of administered cycles was 3.5 (range: 1 - 12). The overall response rate was 13%, with 13 partial responders. The median time to progression was 13.5 weeks (range: 3 - 56; 95% CI = 12 - 14). The median survival was 32 weeks (range: 4 - 104; 95% CI = 27 - 36). Clinical benefit response was acheived for 26 patients (26%). Grade 3/4 haematological toxicities occurred infrequently (anaemia: 5%; neutropenia: 8% and thrombocytopenia: 3% of patients). Grade 3/4 nonhaematological toxicities were not observed. There were no treatment-related deaths. Gemcitabine treatment of patients with locally advanced or metastatic pancreatic cancer is effective and well-tolerated.
引用
收藏
页码:581 / 586
页数:6
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