Improved survival of patients with hepatocellular carcinoma and compensated hepatitis C virus-related cirrhosis who attained sustained virological response

被引:26
作者
Bruno, Savino [1 ,2 ]
Di Marco, Vito [3 ]
Iavarone, Massimo [4 ]
Roffi, Luigi [5 ]
Boccaccio, Vincenzo [1 ,2 ]
Crosignani, Andrea [6 ]
Cabibbo, Giuseppe [3 ]
Rossi, Sonia [1 ,2 ]
Calvaruso, Vincenza [3 ]
Aghemo, Alessio [4 ]
Giacomelli, Luca [7 ]
Craxi, Antonio [3 ]
Colombo, Massimo [4 ]
Maisonneuve, Patrick [8 ]
机构
[1] Humanitas Univ, Rozzano, Italy
[2] IRCCS Ist Clin Humanitas, Rozzano, Italy
[3] Univ Palermo, Gastroenterol & Hepatol Unit, DiBiMIS, Palermo, Italy
[4] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Gastroenterol & Hepatol Unit, Milan, Italy
[5] ASST Nord Milano, Dept Med, Milan, Italy
[6] AO Santi Paolo & Carlo, Dept Internal Med, Milan, Italy
[7] Univ Genoa, Dept Surg & Integrated Diagnost, Genoa, Italy
[8] European Inst Oncol, Div Epidemiol & Biostat, Milan, Italy
关键词
hepatitis C virus; hepatocellular carcinoma; interferon; survival; sustained virological response; HCV CIRRHOSIS; INTERFERON; MANAGEMENT; RECURRENCE; RIBAVIRIN; RESECTION; OUTCOMES; THERAPY; RISK; NEED;
D O I
10.1111/liv.13452
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BackgroundFew studies examined the outcome of patients with hepatitis C virus (HCV)-related cirrhosis who developed hepatocellular carcinoma (HCC). The relative weight as determinant of death for cancer vs end-stage liver disease (ESLD) and the benefit of HCV eradication remain undefined. This multicentre, retrospective analysis evaluates overall survival (OS), rate of decompensation and tumour recurrence in compensated HCC patients treated with interferon (IFN) according to HCV status since HCC diagnosis. MethodsTwo groups of patients with HCV-related cirrhosis and HCC were followed since HCC diagnosis: (i) compensated cirrhotics with prior sustained virological response (SVR) on IFN-based regimens (N=19); (ii) compensated cirrhotics without SVR (viraemic) (N=156). RESULTSOver a median follow-up of 3.0years since the onset of HCC, OS was longer for HCC patients with SVR than for viraemic patients (log-rank P=.004). The 5-year OS rate was 65.9% in patients with SVR vs 31.9% in viraemic patients. Similar trends were reported for hepatic decompensation (log-rank P=.01) and tumour recurrence (log-rank P=.01). These findings were confirmed at multivariable and propensity score analysis. At propensity analysis, 0/19 compensated patients with SVR died for ESLD vs 7/19 (37%) viraemic patients (P=.004). HCC mortality was similar in the two groups. ConclusionsHepatocellular carcinoma patients with prior SVR and compensated cirrhosis at the time of tumour diagnosis have prolonged OS than viraemic patients. Given the lack of cirrhosis progression, no SVR patient ultimately died for ESLD while this condition appears the main cause of death among viraemic patients.
引用
收藏
页码:1526 / 1534
页数:9
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