Improvements in Survival and Clinical Benefit With Gemcitabine as First-Line Therapy for Patients With Advanced Pancreas Cancer: A Randomized Trial (Reprinted from J Clin Oncol, vol 15, pg 2403-2413, 1997

被引:14
作者
Burris, Howard A., III
Moore, Malcolm J.
Andersen, John
Green, Mark R.
Rothenberg, Mace L.
Modiano, Manuel R.
Cripps, M. Christine
Portenoy, Russell K.
Storniolo, Anna Maria
Tarassoff, Peter
Nelson, Robert
Dorr, F. Andrew
Stephens, C. D.
Von Hoff, Daniel D. [1 ]
机构
[1] Inst Drug Dev, Canc Therapy & Res Ctr, 14960 Omicron Dr, San Antonio, TX 78245 USA
关键词
PHASE-II TRIAL; PREVIOUSLY UNTREATED PATIENTS; HIGH-DOSE LEUCOVORIN; MITOMYCIN-C; ADVANCED ADENOCARCINOMA; 5-FLUOROURACIL; CHEMOTHERAPY; FLUOROURACIL; PAIN; CARCINOMA;
D O I
10.1200/JCO.22.02777
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE: Most patients with advanced pancreas cancer experience pain and must limit their daily activities because of tumor-related symptoms. To date, no treatment has had a significant impact on the disease. In early studies with gemcitabine, patients with pancreas cancer experienced an improvement in disease-related symptoms. Based on those findings, a definitive trial was performed to assess the effectiveness of gemcitabine in patients with newly diagnosed advanced pancreas cancer. PATIENTS AND METHODS: One hundred twenty-six patients with advanced symptomatic pancreas cancer completed a lead-in period to characterize and stabilize pain and were randomized to receive either gemcitabine 1,000 mg/m(2) weekly x 7 followed by 1 week of rest, then weekly x 3 every 4 weeks thereafter (63 patients), or to fluorouracil (5-FU) 600 mg/m(2) once weekly (63 patients). The primary efficacy measure was clinical benefit response, which was a composite of measurements of pain (analgesic consumption and pain intensity), Karnofsky performance status, and weight. Clinical benefit required a sustained (> or = 4 weeks) improvement in at least one parameter without worsening in any others. Other measures of efficacy included response rate, time to progressive disease, and survival. RESULTS: Clinical benefit response was experienced by 23.8% of gemcitabine-treated patients compared with 4.8% of 5-FU-treated patients (P = .0022). The median survival durations were 5.65 and 4.41 months for gemcitabine-treated and 5-FU-treated patients, respectively (P = .0025). The survival rate at 12 months was 18% for gemcitabine patients and 2% for 5-FU patients. Treatment was well tolerated. CONCLUSION: This study demonstrates that gemcitabine is more effective than 5-FU in alleviation of some disease-related symptoms in patients with advanced, symptomatic pancreas cancer. Gemcitabine also confers a modest survival advantage over treatment with 5-FU. (C) 1997 by American Society of Clinical Oncology.
引用
收藏
页码:5482 / 5492
页数:11
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