Screening for Hepatocellular Carcinoma in Chronic Liver Disease A Systematic Review

被引:173
作者
Kansagara, Devan [1 ]
Papak, Joel [2 ]
Pasha, Amirala S. [3 ]
O'Neil, Maya [1 ]
Freeman, Michele [1 ]
Relevo, Rose [1 ]
Quinones, Ana [4 ]
Motu'apuaka, Makalapua [5 ]
Jou, Janice H. [2 ]
机构
[1] Portland VA Med Ctr, Portland, OR 97239 USA
[2] Portland VA Med Ctr, Dept Med, Portland, OR 97239 USA
[3] Oregon Hlth & Sci Univ, Dept Med, Portland, OR 97239 USA
[4] Oregon Hlth & Sci Univ, Portland, OR 97239 USA
[5] Oregon Evidence Based Practice Ctr, Portland, OR 97233 USA
关键词
CIRRHOTIC-PATIENTS; NATURAL-HISTORY; SURVEILLANCE PROGRAM; COST-EFFECTIVENESS; EARLY-DIAGNOSIS; HEPATITIS-C; GROWTH-RATE; CANCER; SURVIVAL; IMPROVES;
D O I
10.7326/M14-0558
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Guidelines recommend routine screening for hepatocellular carcinoma (HCC) in high-risk patients, but the strength of evidence supporting these recommendations is unclear. Purpose: To review the benefits and harms of HCC screening in patients with chronic liver disease. Data Sources: MEDLINE, PsycINFO, and ClinicalTrials.gov from inception to April 2014; Cochrane databases to June 2013; reference lists; and technical advisors. Study Selection: English-language trials and observational studies comparing screening versus no screening, studies of harms, and trials comparing different screening intervals. Data Extraction: Mortality and adverse events were the outcomes of interest. Individual-study quality and the overall strength of evidence were dual-reviewed using published criteria. Data Synthesis: Of 13 801 citations, 22 studies met inclusion criteria. The overall strength of evidence on the effects of screening was very low. One large trial of patients with hepatitis B found decreased HCC mortality with periodic ultrasonographic screening (rate ratio, 0.63 [95% CI, 0.41 to 0.98]), but the study was limited by methodological flaws. Another trial in patients with hepatitis B found no survival benefit with periodic alpha-fetoprotein screening. In 18 observational studies, screened patients had earlier-stage HCC than clinically diagnosed patients, but lead- and length-time biases confounded the effects on mortality. Two trials found no survival differences between shorter (3- to 4-month) and longer (6- to 12-month) screening intervals. Harms of screening were not well-studied. Limitations: Only English-language studies were included. The evidence base is limited by methodological issues and a paucity of trials. Conclusion: There is very-low-strength evidence about the effects of HCC screening on mortality in patients with chronic liver disease. Screening tests can identify early-stage HCC, but whether systematic screening leads to a survival advantage over clinical diagnosis is uncertain.
引用
收藏
页码:261 / +
页数:10
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