首页> 外文期刊>The lancet oncology >Gemcitabine versus cisplatin, epirubicin, fluorouracil, and gemcitabine in advanced pancreatic cancer: a randomised controlled multicentre phase III trial.
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Gemcitabine versus cisplatin, epirubicin, fluorouracil, and gemcitabine in advanced pancreatic cancer: a randomised controlled multicentre phase III trial.

机译:吉西他滨与顺铂,表柔比星,氟尿嘧啶和吉西他滨治疗晚期胰腺癌:一项随机对照的多中心III期临床试验。

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BACKGROUND: Patients with advanced pancreatic adenocarcinoma have a poor response, progression-free survival, and overall survival with standard treatment. We aimed to assess whether a four-drug regimen could improve 4 month progression-free survival compared with gemcitabine alone. METHODS: In a randomised multicentre phase III trial, 52 patients were randomly assigned to 40 mg/m2 cisplatin and 40 mg/m2 epirubicin both given on day 1, 600 mg/m2 gemcitabine given intravenously over 1 h on days 1 and 8, and 200 mg/m2 fluorouracil a day given by continuous infusion on days 1-28 of a 4-week cycle (PEFG regimen), and 47 were assigned to 1000 mg/m2 gemcitabine given intravenously over 30 min once a week for 7 of 8 consecutive weeks in cycle 1 and for 3 of 4 weeks thereafter. The primary endpoint was 4-month progression-free survival. Secondary endpoints were overall survival, objective response, safety, and quality of life. Analyses were by intention to treat. FINDINGS: 51 patients assigned PEFG and 46 assigned gemcitabine alone had disease progression. 49 patients in the PEFG group and 46 in the gemcitabine group died from progressive disease. More patients allocated PEFG than gemcitabine alone were alive without progressive disease at 4 months (60% [95% CI 46-72] vs 28% [17-42]; hazard ratio [HR] 0.46 [0.26-0.79]). 1-year overall survival in the PEFG group was 38.5% (25.3-51.7) and in the gemcitabine group was 21.3% (9.6-33.0; HR 0.68 [0.42-1.09]). More patients assigned PEFG showed disease response than did those assigned gemcitabine (38.5% [25.3-51.7] vs 8.5% [0.5-16.5]; odds ratio 6.60 [2.11-20.60], p=0.0008). More patients in the PEFG group had grade 3-4 neutropenia and thrombocytopenia than in the gemcitabine group (p<0.0001). INTERPRETATION: The PEFG regimen could be considered for treatment of advanced pancreatic adenocarcinoma.
机译:背景:晚期胰腺腺癌患者反应较差,无进展生存期以及标准治疗的总体生存期。我们旨在评估与单独使用吉西他滨相比,四药疗法能否改善4个月无进展生存期。方法:在一项随机的多中心III期临床试验中,将52例患者随机分配至第1天第1天给予40 mg / m2顺铂和40 mg / m2表柔比星,分别在第1天和第8天的1小时内静脉内给予600 mg / m2吉西他滨,以及在4周周期的第1-28天(PEFG方案)连续输注,每天给予200 mg / m2氟尿嘧啶,每周7次连续30次(共8次)中的47次分配给1000 mg / m2吉西他滨,每周30分钟静脉注射周期1中的3周,此后4周中的3周。主要终点为4个月无进展生存期。次要终点是总体生存率,客观反应,安全性和生活质量。分析是按意向进行的。结果:仅接受PEFG治疗的患者有51名,仅接受吉西他滨治疗的患者有46名发生了疾病。 PEFG组的49名患者和吉西他滨组的46名患者死于进行性疾病。在4个月时,分配PEFG的患者比没有单独吉西他滨的患者还活着而没有进行性疾病(60%[95%CI 46-72]比28%[17-42];危险比[HR] 0.46 [0.26-0.79])。 PEFG组的1年总生存率为38.5%(25.3-51.7),吉西他滨组为21.3%(9.6-33.0; HR 0.68 [0.42-1.09])。与接受吉西他滨治疗的患者相比,接受PEFG治疗的患者显示出更多的疾病反应(38.5%[25.3-51.7]对8.5%[0.5-16.5];优势比6.60 [2.11-20.60],p = 0.0008)。与吉西他滨组相比,PEFG组的3-4级中性粒细胞减少和血小板减少症患者更多(p <0.0001)。解释:PEFG方案可考虑用于治疗晚期胰腺癌。

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