首页> 外文期刊>JAMA: the Journal of the American Medical Association >Effect of adjuvant chemotherapy with fluorouracil plus folinic acid or gemcitabine vs observation on survival in patients with resected periampullary adenocarcinoma: The ESPAC-3 periampullary cancer randomized trial
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Effect of adjuvant chemotherapy with fluorouracil plus folinic acid or gemcitabine vs observation on survival in patients with resected periampullary adenocarcinoma: The ESPAC-3 periampullary cancer randomized trial

机译:佐剂化疗与氟尿嘧啶加叶酸或吉西他滨的影响对切除血浆腺癌患者存活的观察:ESPAC-3孕产病随机试验

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Context: Patients with periampullary adenocarcinomas undergo the same resectional surgery as that of patients with pancreatic ductal adenocarcinoma. Although adjuvant chemotherapy has been shown to have a survival benefit for pancreatic cancer, there have been no randomized trials for periampullary adenocarcinomas. Objective: To determine whether adjuvant chemotherapy (fluorouracil or gemcitabine) provides improved overall survival following resection. Design, Setting, and Patients: The European Study Group for Pancreatic Cancer (ESPAC)-3 periampullary trial, an open-label, phase 3, randomized controlled trial ( July 2000-May 2008) in 100 centers in Europe, Australia, Japan, and Canada. Of the 428 patients included in the primary analysis, 297 had ampullary, 96 had bile duct, and 35 had other cancers. Interventions: One hundred forty-four patients were assigned to the observation group, 143 patients to receive 20 mg/m 2 of folinic acid via intravenous bolus injection followed by 425 mg/m2 of fluorouracil via intravenous bolus injection administered 1 to 5 days every 28 days, and 141 patients to receive 1000 mg/m2 of intravenous infusion of gemcitabine once a week for 3 of every 4 weeks for 6 months. Main Outcome Measures: The primary outcome measure was overall survival with chemotherapy vs no chemotherapy; secondary measures were chemotherapy type, toxic effects, progression-free survival, and quality of life. Results: Eighty-eight patients (61%) in the observation group, 83 (58%) in the fluorouracil plus folinic acid group, and 73 (52%) in the gemcitabine group died. In the observation group, the median survival was 35.2 months (95%% CI, 27.2-43.0 months) and was 43.1 (95%, CI, 34.0-56.0) in the 2 chemotherapy groups (hazard ratio, 0.86; (95% CI, 0.66-1.11; χ 2=1.33; P=.25). After adjusting for independent prognostic variables of age, bile duct cancer, poor tumor differentiation, and positive lymph nodes and after conducting multiple regression analysis, the hazard ratio for chemotherapy compared with observation was 0.75 (95% CI, 0.57-0.98; Wald χ 2=4.53, P=.03). Conclusions: Among patients with resected periampullary adenocarcinoma, adjuvant chemotherapy, compared with observation, was not associated with a significant survival benefit in the primary analysis; however, multivariable analysis adjusting for prognostic variables demonstrated a statistically significant survival benefit associated with adjuvant chemotherapy. Trial Registration: clinicaltrials.gov Identifier: NCT00058201.
机译:背景信息:患者患者患者经历与胰腺导管腺癌患者相同的切除术手术。虽然已显示佐剂化疗对胰腺癌的生存效益,但对胰腺癌腺癌没有随机试验。目的:判断辅助化疗(氟尿嘧啶或吉西他滨)是否在切除后提供了改善的整体存活。设计,设定和患者:欧洲胰腺癌(ESPAC)的研究组-3欧洲植物审判,开放标签,第3阶段,随机对照试验(2008年7月 - 2008年5月)在欧洲,澳大利亚,日本,和加拿大。在初级分析中包含的428名患者中,297例患有安瓿,96例胆管,35例含有其他癌症。干预措施:将一百四十四名患者分配到观察组,143名患者通过静脉注射液注射接受20mg / m 2叶酸叶酸,然后通过静脉注射喷射液体注射425mg / m 2氟尿嘧啶给药1至5天天和141名患者每4周每隔4周接受每周3000mg / m2的静脉内输注吉西他滨一次。主要结果措施:主要结果措施与化疗的总体生存率与化疗;次要措施是化疗类型,毒性效应,无进展的生存和生活质量。结果:88名患者(61%)在观察组,83(58%)在氟尿嘧啶加枯草基团中,吉西他滨集团的73(52%)死亡。在观察组中,中位存活率为35.2个月(95 %% CI,27.2-43.0个月),23.1(95%,CI,34.0-56.0)中,在2组(危险比0.86;(95%CI) ,0.66-1.11;χ2= 1.33; p = .25)。调整年龄的独立预后变量,胆管癌,肿瘤癌,差异淋巴结差和进行多元回归分析后,危险比化疗的危害比相比观察为0.75(95%CI,0.57-0.98; WALDχ2= 4.53,P = .03)。结论:与观察结果相比,辅助化疗的患者均未与显着的生存效益相关主要分析;然而,对预后变量调整的多变量分析表明,与佐剂化疗相关的统计上显着的存活益处。试验注册:ClinicalTrials.gov标识符:NCT00058201。

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  • 作者单位

    Liverpool Cancer Trials Unit Cancer Research United Kingdom Centre University of Liverpool;

    Division of Medical Oncology and Hematology Department of Medicine Princess Margaret Hospital;

    Liverpool Cancer Trials Unit Cancer Research United Kingdom Centre University of Liverpool;

    Manchester Academic Health Sciences Centre Christie NHS Foundation Trust University of Manchester;

    Cancer Research UK Institute for Cancer Studies Queen Elizabeth Hospital University Hospital;

    Beatson West of Scotland Cancer Centre Glasgow United Kingdom;

    Department of Surgery Glasgow Royal Infirmary Glasgow United Kingdom;

    Ludwig Oncology Unit Austin Health Melbourne VIC Australia;

    Department of Surgery Agia Olga Hospital Athens Greece;

    Medical Oncology Clatterbridge Centre for Oncology Clatterbridge Road Bebington Merseyside;

    Department of Oncology Akademiska Sjukhuset Uppsala University Uppsala Sweden;

    Department of Surgery Freeman Hospital Newcastle upon Tyne United Kingdom;

    Service de Chirurgie Digestive et Viscérale H?pital Tenon Paris France;

    Cross Cancer Institute Edmonton AB Canada;

    Department of Oncology Churchill Hospital Oxford University Hospitals NHS Trust Oxford United;

    Department of Oncology St. James's University Hospital Leeds United Kingdom;

    Liverpool Cancer Trials Unit Cancer Research United Kingdom Centre University of Liverpool;

    Liverpool Cancer Trials Unit Cancer Research United Kingdom Centre University of Liverpool;

    Department of Medicine Ernst-Moritz-Arndt-Universit?t Greifswald Greifswald Germany;

    Department of Surgery Petz Aladar Hospital Gyor Hungary;

    Liverpool Cancer Trials Unit Cancer Research United Kingdom Centre University of Liverpool;

    Department of Pathology Karolinska University Hospital Stockholm Sweden;

    Liverpool Cancer Trials Unit Cancer Research United Kingdom Centre University of Liverpool;

    Department of Surgery University of Heidelberg Heidelberg Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医药、卫生;
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