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首页> 外文期刊>European journal of cancer: official journal for European Organization for Research and Treatment of Cancer (EORTC) [and] European Association for Cancer Research (EACR) >Multicentre randomised phase III trial comparing Tamoxifen alone or with Transarterial Lipiodol Chemoembolisation for unresectable hepatocellular carcinoma in cirrhotic patients (Federation Francophone de Cancerologie Digestive 9402).
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Multicentre randomised phase III trial comparing Tamoxifen alone or with Transarterial Lipiodol Chemoembolisation for unresectable hepatocellular carcinoma in cirrhotic patients (Federation Francophone de Cancerologie Digestive 9402).

机译:一项多中心随机III期试验,比较了他莫昔芬单独或与经动脉血脂碘化化学栓塞治疗肝硬化患者不可切除的肝细胞癌(联邦法语国家癌症研究消化系统9402)。

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The FFCD 9402 multicentre phase III trial was designed to compare the effects of the combination of Transarterial Lipiodol Chemoembolisation (TACE) and tamoxifen with tamoxifen alone on overall survival and quality of life in the palliative treatment of hepatocellular carcinoma with cirrhosis. From 1995 to 2002, 138 patients were randomised between the two groups. One hundred and twenty three patients were eligible including 61 in the Tamoxifen group and 62 in the TACE group. Baseline characteristics were similar: Child-Pugh class A: 70%, alcoholic cirrhosis: 76%, Okuda stage I: 71%, multinodular tumour: 70% and segmental portal vein thrombosis: 10%. At 2years, the overall survival was 22% and 25% in the Tamoxifen and TACE groups (P=.68), respectively. Multivariate analysis identified four independent prognostic factors for survival: alpha-fetoprotein (AFP)>400ng/mL (P=.008), abdominal pain (P=.011), hepatomegaly (P=.023) and Child-Pugh score (P=.032). The Spitzer Index level assessing the quality of life during follow-up did not differ between the two groups (P=.70). Amongst patients with stage Okuda I, the 2-year overall survival was 28% in the Tamoxifen group and 32% in the TACE group (P=.58). In this subgroup, two prognostic factors were statistically significant for survival: AFP>400ng/mL (P=.004) and Spitzer Index (P=.013) as shown by multivariable analysis. In conclusion, this study suggests that TACE improves neither the survival nor the quality of life in patients with HCC and cirrhosis.
机译:FFCD 9402多中心III期临床试验旨在比较肝动脉硬化性肝癌姑息治疗中经动脉血脂碘化化学栓塞(TACE)和他莫昔芬与单独他莫昔芬的组合对总体生存和生活质量的影响。从1995年到2002年,在两组之间随机分配了138例患者。 123例患者符合条件,其中他莫昔芬组为61例,TACE组为62例。基线特征相似:Child-Pugh A级:70%,酒精性肝硬化:76%,奥田I期:71%,多结节性肿瘤:70%,门静脉段血栓形成:10%。在2年时,他莫昔芬和TACE组的总生存率分别为22%和25%(P = .68)。多因素分析确定了四个独立的生存预后因素:甲胎蛋白(AFP)> 400ng / mL(P = .008),腹痛(P = .011),肝肿大(P = .023)和Child-Pugh评分(P = .032)。两组之间评估生活质量的Spitzer指数水平在两组之间没有差异(P = .70)。在Okuda I期患者中,他莫昔芬组的2年总生存率为28%,TACE组为32%(P = .58)。在该亚组中,两个预后因素对生存率具有统计学意义:如多变量分析所示,AFP> 400ng / mL(P = .004)和Spitzer Index(P = .013)。总之,这项研究表明,TACE不能改善HCC和肝硬化患者的生存率或生活质量。

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