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首页> 外文期刊>The Lancet >Adjuvant chemoradiotherapy and chemotherapy in resectable pancreatic cancer: a randomised controlled trial.
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Adjuvant chemoradiotherapy and chemotherapy in resectable pancreatic cancer: a randomised controlled trial.

机译:可切除的胰腺癌的辅助放化疗和化疗:一项随机对照试验。

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BACKGROUND: The role of adjuvant treatment in pancreatic cancer remains uncertain. The European Study Group for Pancreatic Cancer (ESPAC) assessed the roles of chemoradiotherapy and chemotherapy in a randomised study. METHODS: After resection, patients were randomly assigned to adjuvant chemoradiotherapy (20 Gy in ten daily fractions over 2 weeks with 500 mg/m(2) fluorouracil intravenously on days 1-3, repeated after 2 weeks) or chemotherapy (intravenous fluorouracil 425 mg/m(2) and folinic acid 20 mg/m(2) daily for 5 days, monthly for 6 months). Clinicians could randomise patients into a two-by-two factorial design (observation, chemoradiotherapy alone, chemotherapy alone, or both) or into one of the main treatment comparisons (chemoradiotherapy versus no chemoradiotherapy or chemotherapy versus no chemotherapy). The primary endpoint was death, and all analyses were by intention to treat.Findings 541 eligible patients with pancreatic ductal adenocarcinoma were randomised: 285 in the two-by-two factorial design (70 chemoradiotherapy, 74 chemotherapy, 72 both, 69 observation); a further 68 patients were randomly assigned chemoradiotherapy or no chemoradiotherapy and 188 chemotherapy or no chemotherapy. Median follow-up of the 227 (42%) patients still alive was 10 months (range 0-62). Overall results showed no benefit for adjuvant chemoradiotherapy (median survival 15.5 months in 175 patients with chemoradiotherapy vs 16.1 months in 178 patients without; hazard ratio 1.18 [95% CI 0.90-1.55], p=0.24). There was evidence of a survival benefit for adjuvant chemotherapy (median survival 19.7 months in 238 patients with chemotherapy vs 14.0 months in 235 patients without; hazard ratio 0.66 [0.52-0.83], p=0.0005).Interpretation This study showed no survival benefit for adjuvant chemoradiotherapy but revealed a potential benefit for adjuvant chemotherapy, justifying further randomised controlled trials of adjuvant chemotherapy in pancreatic cancer.
机译:背景:辅助治疗在胰腺癌中的作用仍不确定。欧洲胰腺癌研究小组(ESPAC)在一项随机研究中评估了放化疗和化疗的作用。方法:切除后,患者被随机分配到辅助放化疗中(2-3周内,每天10次,每次20 Gy,在1-3天静脉滴注500 mg / m(2)氟尿嘧啶,两周后重复)或化疗(静脉内氟尿嘧啶425 mg / m(2)和亚叶酸20 mg / m(2)每天5天,每月6个月)。临床医生可以将患者随机分为两因素分析设计(观察,仅放化疗,单独使用化疗或两者兼有)或进行主要治疗比较之一(放化疗与无放化疗或放化疗与无化疗)。研究的主要终点是死亡,所有分析均按治疗意愿进行。研究结果对541例符合条件的胰腺导管腺癌患者进行了随机分组:二乘二因子设计285例(放化疗70例,化疗74例,两者72例,观察69例)。另有68例患者被随机分配放化疗或不放化疗和188化疗或不放化疗。仍然活着的227名(42%)患者的中位随访时间为10个月(范围0-62)。总体结果显示辅助化学放疗没有益处(175例接受化学放疗的患者中位生存期为15.5个月,而无178例接受化疗的患者的中位生存期为16.1个月;危险比为1.18 [95%CI 0.90-1.55],p = 0.24)。有证据显示辅助化疗可提高生存率(238例接受化疗的患者中位生存期为19.7个月,而无化疗的235例患者中位生存期为14.0个月;危险比为0.66 [0.52-0.83],p = 0.0005)。辅助放化疗,但显示了辅助化疗的潜在益处,证明了胰腺癌辅助化疗的进一步随机对照试验是合理的。

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