Waziry Reem, Grebely Jason, Amin Janaki, Alavi Maryam, Hajarizadeh Behzad, George Jacob, Matthews Gail V, Law Matthew, Dore Gregory J
The Kirby Institute UNSW Sydney Sydney Australia.
Faculty of Medicine and Health Sciences Macquarie University Sydney Australia.
Hepatol Commun. 2017 Aug 16;1(8):736-747. doi: 10.1002/hep4.1073. eCollection 2017 Oct.
We assessed trends in HCC survival in patients with hepatitis B virus (HBV) or hepatitis C virus (HCV) infection in New South Wales, Australia. Data on HBV (n = 54,399) and HCV (n = 96,908) notifications (1993-2012) were linked to a hospitalization database (July 2000-June 2014), the New South Wales Cancer Registry, and the New South Wales Death Registry. A total of 725 (1.3%) first HBV-hepatocellular carcinoma (HCC) and 1,309 (1.4%) first HCV-HCC hospitalizations were included. Death occurred in 60.4% of HBV-HCC and 69.6% of HCV-HCC patients. Median survival following first HBV-HCC hospitalization improved from 0.6 years (95% confidence interval [CI] 0.39-1.28) in 2000-2004 to 2.8 years (1.54-5.54) in 2010-2014. Median survival following first HCV-HCC hospitalization was 0.8 years (0.45-1.33) in 2000-2004 and 0.9 (0.67-1.18) in 2010-2014. One-year HBV-HCC survival in 2010-2014 compared to 2000-2004 improved for those with (94% versus 81%) and without (42% versus 33%) potentially curative procedures (liver resection, liver transplantation, and radiofrequency ablation). Factors associated with improved survival following HBV-HCC were later study period (hazard ratio [HR] = 0.74; 95% CI, 0.57-0.97) and potentially curative procedures (liver resection, liver transplantation, and radiofrequency ablation) (HR = 0.23; 95% CI, 0.17-0.29), while male gender (HR = 1.37; 95% CI, 1.03-1.82), human immunodeficiency virus coinfection (HR = 3.06; 95% CI, 1.36-6.88), and Charlson Comorbidity Index ≥3 (HR = 1.81; 95% CI, 1.35-2.40) were associated with reduced survival. Factors associated with improved survival following HCC-HCV were Asia-Pacific country of birth (HR = 0.68; 95% CI, 0.55-0.84) and potentially curative procedures (HR = 0.21; 95% CI, 0.17-0.25), while age (HR = 1.01; 95% CI, 1.01-1.02), rural place of residence (HR = 1.46; 95% CI, 1.22-1.74), and human immunodeficiency virus coinfection (HR = 2.71; 95% CI, 1.19-6.15) were associated with reduced survival. : All-cause survival following HBV-HCC has improved considerably, suggesting an impact of more effective antiviral therapy and earlier HCC diagnosis; in contrast, all-cause survival for HCV-HCC is unchanged. ( 2017;1:736-747).
我们评估了澳大利亚新南威尔士州乙型肝炎病毒(HBV)或丙型肝炎病毒(HCV)感染患者的肝癌生存趋势。将1993 - 2012年HBV(n = 54,399)和HCV(n = 96,908)报告的数据与一个住院数据库(2000年7月 - 2014年6月)、新南威尔士州癌症登记处以及新南威尔士州死亡登记处进行了关联。总共纳入了725例(1.3%)首次HBV相关肝细胞癌(HCC)住院病例和1309例(1.4%)首次HCV相关HCC住院病例。60.4%的HBV相关HCC患者和69.6%的HCV相关HCC患者死亡。首次HBV相关HCC住院后的中位生存期从2000 - 2004年的0.6年(95%置信区间[CI] 0.39 - 1.28)提高到2010 - 2014年的2.8年(1.54 - 5.54)。首次HCV相关HCC住院后的中位生存期在2000 - 2004年为0.8年(0.45 - 1.33),在2010 - 2014年为0.9年(0.67 - 1.18)。与2000 - 2004年相比,2010 - 2014年接受(94%对81%)和未接受(42%对33%)潜在治愈性手术(肝切除、肝移植和射频消融)患者的HBV相关HCC的1年生存率有所提高。与HBV相关HCC生存改善相关的因素包括研究时期较晚(风险比[HR] = 0.74;95% CI,0.57 - 0.97)和潜在治愈性手术(HR = 0.23;95% CI,0.17 - 0.29),而男性(HR = 1.37;95% CI,1.03 - 1.82)、人类免疫缺陷病毒合并感染(HR = 3.06;95% CI,1.36 - 6.88)以及Charlson合并症指数≥3(HR = 1.81;95% CI,1.35 - 2.40)与生存率降低相关。与HCV相关HCC生存改善相关的因素包括出生于亚太国家(HR = 0.68;95% CI,0.55 - 0.84)和潜在治愈性手术(HR = 0.21;95% CI,0.17 - 0.25),而年龄(HR = 1.01;95% CI,1.01 - 1.02)、农村居住地(HR = 1.46;95% CI,1.22 - 1.74)以及人类免疫缺陷病毒合并感染(HR = 2.71;95% CI,1.19 - 6.15)与生存率降低相关:HBV相关HCC的全因生存率有显著提高,提示更有效的抗病毒治疗和更早的肝癌诊断产生了影响;相比之下,HCV相关HCC的全因生存率未变。(2017;1:736 - 747)