Natural History of Untreated Nonsurgical Hepatocellular Carcinoma: Rationale for the Design and Evaluation of Therapeutic Trials

肝细胞癌 医学 阶段(地层学) 内科学 不利影响 自然史 胃肠病学 随机对照试验 肝病 前瞻性队列研究 多元分析 外科 预后变量 肝硬化 临床试验 疾病 肿瘤科 家族史 性能状态 生存分析 酒精性肝病 总体生存率 自然史研究 癌症 存活率 比例危险模型
作者
Josep M. Llovet,Javier Bustamante,Antoni Castells,R. Vilana,Maria Del Carmen Ayuso,María Sala,Concepció Brú,Joan Rodés,Jordi Bruix
出处
期刊:Hepatology [Lippincott Williams & Wilkins]
卷期号:29 (1): 62-67 被引量:1182
标识
DOI:10.1002/hep.510290145
摘要

This study analyzed the natural history and prognostic factors of patients with nonsurgical hepatocellular carcinoma (HCC). Twenty variables from 102 cirrhotic patients with HCC who were not treated within prospective randomized controlled trials (RCT) were investigated through uni– and multivariate analyses. None of them was suitable for radical therapies (surgical resection, liver transplantation, or ethanol injection) or presented end–stage disease as reflected by an Okuda stage 3 or a Performance Status ≥3. Sixty–five patients were Child–Pugh A, 34 were B, and 3 were C. Most of them exhibited a preserved Performance Status Test (PST) (0 = 56; 1 = 38; 2 = 8). Tumor was solitary in 26 (≤5 cm in 16) and multinodular/massive in 76. After a median follow–up of 17 months, 79 patients died, the 1–, 2–, and 3–year survival being 54%, 40%, and 28%. The multivariate study identified PST ( P = .01), constitutional syndrome ( P = .04), vascular invasion ( P = .001), and extrahepatic spread ( P = .04) as independent predictors for mortality. The 1–, 2–, and 3–year survival for the 48 patients without adverse factors (Stage 0) was 80%, 65%, and 50%, respectively, and 29%, 16%, and 8% in the 54 patients with at least one adverse parameter (Stage I). Therefore, Stage 0 would correspond to an intermediate stage, while Stage I would represent an advanced status, before reaching an end–stage phase. In conclusion, the outcome of nonsurgical HCC is not homogeneously grim and may be predicted by assessing the presence of symptoms and of an invasive tumoral pattern. Therapeutic trials should be designed and evaluated considering these characteristics.
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