Surveillance improves survival of patients with hepatocellular carcinoma: a prospective population-based study

被引:43
|
作者
Hong, Thai P. [1 ]
Gow, Paul J. [2 ]
Fink, Michael [3 ,4 ]
Dev, Anouk [5 ]
Roberts, Stuart K. [2 ]
Nicoll, Amanda [6 ]
Lubel, John S. [6 ]
Kronborg, Ian [7 ]
Arachchi, Niranjan [7 ]
Ryan, Marno [1 ]
Kemp, William W. [8 ]
Knight, Virginia [5 ]
Sundararajan, Vijaya [3 ]
Desmond, Paul [1 ]
Thompson, Alexander J., V [1 ]
Bell, Sally J. [1 ]
机构
[1] St Vincents Hosp Melbourne, Melbourne, Vic, Australia
[2] Austin Hosp, Melbourne, Vic, Australia
[3] Univ Melbourne, Melbourne, Vic, Australia
[4] Austin Hlth, Melbourne, Vic, Australia
[5] Monash Hlth, Melbourne, Vic, Australia
[6] Eastern Hlth, Melbourne, Vic, Australia
[7] Western Hlth, Melbourne, Vic, Australia
[8] Alfred Hosp, Melbourne, Vic, Australia
关键词
RANDOMIZED CONTROLLED-TRIAL; LIVER-CANCER; HEPATITIS-B; UNITED-STATES; EPIDEMIOLOGY; TRENDS; IMPACT;
D O I
10.5694/mja18.00373
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: To determine the factors associated with survival of patients with hepatocellular carcinoma (HCC) and the effect of HCC surveillance on survival. Design, setting and participants: Prospective population-based cohort study of patients newly diagnosed with HCC in seven tertiary hospitals in Melbourne, 1 July 2012 - 30 June 2013. Main outcome measures: Overall survival (maximum follow-up, 24 months); factors associated with HCC surveillance participation and survival. Results: 272 people were diagnosed with incident HCC during the study period; the most common risk factors were hepatitis C virus infection (41%), alcohol-related liver disease (39%), and hepatitis B virus infection (22%). Only 40% of patients participated in HCC surveillance at the time of diagnosis; participation was significantly higher among patients with smaller median tumour size (participants, 2.8 cm; non-participants, 6.0 cm; P < 0.001) and earlier Barcelona Clinic Liver Cancer (BCLC) stage disease (A/B, 59%; C/D, 25%; P < 0.001). Participation was higher among patients with compensated cirrhosis or hepatitis C infections; it was lower among those with alcohol-related liver disease or decompensated liver disease. Median overall survival time was 20.8 months; mean survival time was 18.1 months (95% CI, 16.6-19.6 months). Participation in HCC surveillance was associated with significantly lower mortality (adjusted hazard ratio [aHR], 0.60; 95% CI, 0.38-0.93; P = 0.021), as were curative therapies (aHR, 0.33; 95% CI, 0.19-0.58). Conversely, higher Child-Pugh class, alpha-fetoprotein levels over 400 kU/L, and later BCLC disease stages were each associated with higher mortality. Conclusions: Survival for patients with HCC is poor, but may be improved by surveillance, associated with the identification of earlier stage tumours, enabling curative therapies to be initiated.
引用
收藏
页码:348 / 354
页数:7
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