Sofosbuvir-based regimens for HCV in stage 4-stage 5 chronic kidney disease. A systematic review with meta-analysis

被引:1
|
作者
Fabrizi, Fabrizio [1 ,2 ]
Cerutti, Roberta [1 ,2 ]
Dixit, Viva [3 ]
Ridruejo, Ezequiel [4 ,5 ,6 ]
机构
[1] IRCCS Ca Granda Fdn, Div Nephrol Dialysis & Transplantat, Milan, Italy
[2] Maggiore Polyclyn Hosp, Milan, Italy
[3] UCLA, Div Digest Dis, Sch Med, Los Angeles, CA USA
[4] Ctr Educ Medial & Invest Clin Norberto Quirno CEM, Dept Med, Hepatol Sect, Ciudad Autonoma De Buoen, Argentina
[5] Hosp Univ Austral, Hepatol & Liver Transplant Unit, Pilar, Provincia De Bu, Argentina
[6] Latin Amer Liver Res Educ & Awareness Network LAL, Pilar, Provincia De Bu, Argentina
来源
NEFROLOGIA | 2021年 / 41卷 / 05期
关键词
Adverse events; Dialysis; Direct-acting antivirals; Hepatitis C; Sofosbuvir; Virological response; CHRONIC HEPATITIS-C; DOSE SOFOSBUVIR; VIRUS-INFECTION; RENAL-DISEASE; EFFICACY; SAFETY; THERAPY; EXPERIENCE;
D O I
10.1016/j.nefroe.2021.11.011
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Hepatitis C is an important agent of liver damage in patients with chronic kidney disease and the advent of DAAs has dramatically changed the management of HCV positive patients, including those with advanced CKD. Sofosbuvir is the backbone of many anti-HCV regimens based on DAAs but it remains unclear whether it is appropriate for HCV-infected patients with stage 4-5 CKD. Study aims and design: We performed a systematic review of the literature with a meta-analysis of clinical studies in order to evaluate the efficacy and safety of SOF-based DAA regimens in patients with stage 4-5 CKD. The primary outcome was sustained viral response (as a measure of efficacy); the secondary outcomes were the frequency of SAEs and dropouts due to AEs (as measures of tolerability). The random-effects model of DerSimonian and Laird was adopted, with heterogeneity and stratified analyses. Results: Thirty clinical studies (n = 1537 unique patients) were retrieved. The pooled SVR12 and SAEs rate was 0.99 (95% confidence intervals, 0.97; 1.0, I-2 = 99.8%) and 0.09 (95% CI, 0.05; 0.13, I-2 = 84.3%), respectively. The pooled SVR12 rate in studies with high HCV RNA levels at baseline was lower, 0.87 (95% CI, 0.75; 1.0, I-2 = 73.3%) (P < 0.001). The pooled drop-out rate due to AEs was 0.02 (95% CI, -0.01; 0.04, I-2 = 16.1%). Common serious adverse events were anemia (n = 26, 38%) and reduced eGFR (n = 14, 19%). SAEs were more common in studies adopting full-dose sofosbuvir (pooled rate of SAEs 0.15, 95% CI, 0.06; 0.25; I-2 = 80.1%) and in those based on ribavirin (0.15, 95% CI, 0.07; 0.23, I-2 = 95.8%). Six studies (n = 69 patients) reported eGFR levels at baseline/post- antiviral therapy; no consistent changes were found. Conclusions: SOF-based regimens appear safe and effective in patients with stage 4-5 CKD. Serum creatinine should be carefully monitored during therapy with SOF in patients with CKD. Randomized controlled studies in order to expand our knowledge on this point are under way. (C) 2021 Sociedad Espanola de Nefrologia. Published by Elsevier Espana, S.L.U.
引用
收藏
页码:578 / 589
页数:12
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