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首页> 外文期刊>British Journal of Cancer >Phase II study of weekly oxaliplatin plus infusional fluorouracil and folinic acid (FUFOX regimen) as first-line treatment in metastatic gastric cancer
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Phase II study of weekly oxaliplatin plus infusional fluorouracil and folinic acid (FUFOX regimen) as first-line treatment in metastatic gastric cancer

机译:每周一次奥沙利铂联合输注氟尿嘧啶和亚叶酸(FUFOX方案)II期研究用于转移性胃癌的一线治疗

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Oxaliplatin plus fluorouracil/folinic acid (5-FU/FA) every 2 weeks has shown promising activity in advanced gastric cancer. This study assessed the efficacy and safety of weekly oxaliplatin plus 5-FU/FA (FUFOX regimen) in the metastatic setting. Patients with previously untreated metastatic gastric cancer received oxaliplatin (50?mg?m?2) plus FA (500?mg?m?2, 2-h infusion) followed by 5-FU (2000?mg?m?2, 24-h infusion) given on days 1, 8, 15 and 22 of a 5-week cycle. The primary end point of this multicentre phase II study was the response rate according to RECIST criteria. A total of 48 patients were enrolled. Median age was 62 years and all patients had metastatic disease, with a median number of three involved organs. The most common treatment-related grade 3/4 adverse events were diarrhoea (17%), deep vein thrombosis (15%), neutropenia (8%), nausea (6%), febrile neutropenia (4%), fatigue (4%), anaemia (4%), tumour bleeding (4%), emesis (2%), cardiac ischaemia (2%) and pneumonia (2%). Grade 1/2 sensory neuropathy occurred in 67% of patients but there were no episodes of grade 3 neuropathy. Intent-to-treat analysis showed a response rate of 54% (95% CI, 39–69%), including two complete responses. At a median follow-up of 18.1 months (range 11.2–26.2 months), median survival is 11.4 months (95% CI, 8.0–14.9 months) and the median time to progression is 6.5 months (95% CI, 3.9–9.2 months). The weekly FUFOX regimen is well tolerated and shows notable activity as first-line treatment in metastatic gastric cancer.
机译:奥沙利铂加氟尿嘧啶/亚叶酸(5-FU / FA)每2周显示在晚期胃癌中有希望的活性。这项研究评估了每周一次奥沙利铂联合5-FU / FA(FUFOX方案)在转移性环境中的疗效和安全性。先前未经治疗的转移性胃癌患者先接受奥沙利铂(50?mg?m?2),FA(500?mg?m?2、2小时输注),然后接受5-FU(2000?mg?m?2、24小时)。 h输注)在5周周期的第1、8、15和22天进行。这项多中心II期研究的主要终点是根据RECIST标准的反应率。共有48位患者入选。中位年龄为62岁,所有患者均患有转移性疾病,中位三个受累器官。与治疗相关的最常见的3/4级不良事件为腹泻(17%),深静脉血栓形成(15%),中性粒细胞减少症(8%),恶心(6%),发热性中性粒细胞减少症(4%) ,疲劳(4%),贫血(4%),肿瘤出血(4%),呕吐(2%),心脏缺血(2%)和肺炎(2%)。 67%的患者发生1/2级感觉神经病变,但没有3级神经病变发作。意向治疗分析显示反应率为54%(CI为95%,39-69%),包括两个完整的反应。中位随访期为18.1个月(范围为11.2-26.2个月),中位生存期为11.4个月(95%CI,8.0-14.9个月),中位进展时间为6.5个月(95%CI,3.9-5%)。 9.2个月)。每周的FUFOX方案耐受性良好,在转移性胃癌中作为一线治疗表现出显着活性。

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