Factors influencing the failure of interferon-free therapy for chronic hepatitis C: Data from the Polish EpiTer-2 cohort study

被引:11
作者
Janczewska, Ewa [1 ]
Kolek, Mateusz Franciszek [2 ]
Lorenc, Beata [3 ]
Klapaczynski, Jakub [4 ]
Tudrujek-Zdunek, Magdalena [5 ]
Sitko, Marek [6 ]
Mazur, Wlodzimierz [7 ]
Zarebska-Michaluk, Dorota [8 ]
Buczynska, Iwona [9 ]
Dybowska, Dorota [10 ]
Czau-Anderzejuk, Agnieszka [11 ]
Berak, Hanna [12 ]
Krygier, Rafal [13 ]
Jaroszewicz, Jerzy [14 ]
Citko, Jolanta [15 ]
Piekarska, Anna [16 ]
Dobracka, Beata [17 ]
Socha, Lukasz [18 ]
Deron, Zbigniew [19 ]
Laurans, Lukasz [18 ,20 ]
Bialkowska-Warzecha, Jolanta [21 ]
Tronina, Olga [22 ]
Adamek, Brygida [1 ]
Tomasiewicz, Krzysztof [5 ]
Simon, Krzysztof [9 ]
Pawlowska, Malgorzata [23 ]
Halota, Waldemar [10 ]
Flisiak, Robert [11 ]
机构
[1] Med Univ Silesia, Sch Hlth Sci Bytom, Dept Basic Med Sci, Piekarska 18, PL-41902 Bytom, Poland
[2] Univ Warsaw, Fac Biol, Dept Anim Physiol, PL-02096 Warsaw, Poland
[3] Med Univ Gdansk, Pomeranian Ctr Infect Dis, PL-80214 Gdansk, Poland
[4] Minist Internal Affairs & Adm, Dept Internal Med & Hepatol, Cent Clin Hosp, PL-02507 Warsaw, Poland
[5] Med Univ Lublin, Dept Infect Dis, PL-20081 Lublin, Poland
[6] Jagiellonian Univ, Dept Infect & Trop Dis, PL-30688 Krakow, Poland
[7] Med Univ Silesia, Clin Dept Infect Dis, PL-41500 Chorzow, Poland
[8] Jan Kochanowski Univ Kielce, Dept Infect Dis, PL-25369 Kielce, Poland
[9] Med Univ Wroclaw, Dept Infect Dis & Hepatol, PL-51149 Wroclaw, Poland
[10] Nicolaus Copernicus Univ Torun, Dept Infect Dis & Hepatol, Fac Med, Ludwik Rydygier Coll Med Bydgoszcz, PL-85030 Bydgoszcz, Poland
[11] Med Univ Bialystok, Dept Infect Dis & Hepatol, PL-15540 Bialystok, Poland
[12] Hosp Infect Dis Warsaw, Day Dept 1, PL-01201 Warsaw, Poland
[13] State Univ Appl Sci Konin, Outpatient Clin, PL-62510 Konin, Poland
[14] Med Univ Silesia, Dept Infect Dis & Hepatol, PL-41902 Bytom, Poland
[15] Reg Hosp, Dept Med Practice Infect, PL-10561 Olsztyn, Poland
[16] Med Univ Lodz, Dept Infect Dis & Hepatol, PL-90419 Lodz, Poland
[17] MedicalSpec Ctr, PL-53428 Wroclaw, Poland
[18] Pomeranian Med Univ, Dept Infect Dis Hepatol & Liver Transplantat, PL-71455 Szczecin, Poland
[19] Bieganski Reg Specialist Hosp, Ward Infect Dis & Hepatol, PL-91347 Lodz, Poland
[20] Multidisciplinary Reg Hosp, Infect & Liver Dis Clin, PL-66400 Gorzow Wielkopolski, Poland
[21] Med Univ Lodz, Dept Infect & Liver Dis, PL-91347 Lodz, Poland
[22] Med Univ Warsaw, Dept Transplantat Med Nephrol & Internal Dis, PL-02091 Warsaw, Poland
[23] Nicolaus Copernicus Univ Torun, Coll Med Bydgoszcz, Fac Med, Dept Paediat Infect Dis & Hepatol, PL-85030 Bydgoszcz, Poland
关键词
Advanced liver disease; Chronic hepatitis C; Direct-acting antiviral drugs; Sustained virologic response; Interferon-free therapy; Antiviral therapy; DIRECT-ACTING ANTIVIRALS; NUCLEOTIDE POLYMERASE INHIBITOR; REAL CLINICAL-PRACTICE; GENOTYPE; SOFOSBUVIR; INFECTION; DACLATASVIR; ASUNAPREVIR; RIBAVIRIN; SAFETY;
D O I
10.3748/wjg.v27.i18.2177
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND The introduction of direct-acting antiviral drugs into clinical practice has revolutionized the treatment of chronic hepatitis C, making it highly effective and safe for patients. However, few researchers have analyzed the factors causing therapy failure in some patients. AIM To analyze factors influencing the failure of direct antiviral drugs in the large, multicenter EpiTer-2 cohort in a real-world setting. METHODS The study cohort consisted of patients with chronic hepatitis C treated at 22 Polish centers from 2016-2020. Data collected from the online EpiTer-2 database included the following: hepatitis C virus (HCV) genotype, stage of fibrosis, hematology and liver function parameters, Child-Turcotte-Pugh and Model for End-stage Liver Disease scores, prior antiviral therapy, concomitant diseases, and drugs used in relation to hepatitis B virus (HBV) and/or human immunodeficiency virus (HIV) coinfections. Adverse events observed during the treatment and follow-up period were reported. Both standard and machine learning methods were used for statistical analysis. RESULTS During analysis, 12614 patients with chronic hepatitis C were registered, of which 11938 (mean age: 52 years) had available sustained virologic response (SVR) data [11629 (97%) achieved SVR and 309 (3%) did not]. Most patients (78.1%) were infected with HCV genotype 1b. Liver cirrhosis was diagnosed in 2974 patients, while advanced fibrosis (F3) was diagnosed in 1717 patients. We included patients with features of hepatic failure at baseline [ascites in 142 (1.2%) and encephalopathy in 68 (0.6%) patients]. The most important host factors negatively influencing treatment efficacy were liver cirrhosis, clinical and laboratory features of liver failure, history of hepatocellular carcinoma, and higher body mass index. Among viral factors, genotype 3 and viral load also exerted an influence on treatment efficacy. Classical statistical analysis revealed that treatment ineffectiveness seemed to be influenced by the male sex, which was not confirmed by the multivariate analysis using the machine learning algorithm (random forest). Coinfection with HBV (including patients with on-treatment reactivation of HBV infection) or HIV, extrahepatic manifestations, and renal failure did not significantly affect the treatment efficacy. CONCLUSION In patients with advanced liver disease, individualized therapy (testing for resistance-associated variants and response-guided treatment) should be considered to maximize the chance of achieving SVR.
引用
收藏
页码:2177 / 2192
页数:16
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