Evidence reviews for the US Preventive Services Task Force (USPSTF) use an analytic framework to visually display the key questions that the review will address to allow the USPSTF to evaluate the effectiveness and safety of a preventive service. The questions are depicted by linkages that relate interventions and outcomes. A dashed line indicates a health outcome that immediately follows an intermediate outcome. See USPSTF Procedure Manual.7 HCV indicates hepatitis C virus; SVR, sustained virologic response.
aIncludes persons without abnormal laboratory values. Adolescents are defined as those aged 12 to 17 years. Excludes persons living with HIV, transplant recipients, and patients with renal failure.
bDefined as HCV antibody testing with confirmatory HCV RNA testing as indicated.
cIncludes interventions that may affect vertical transmission of HCV, such as cesarean delivery, amniocentesis, fetal monitoring, management of ruptured membranes, breastfeeding, and antiviral treatment.
dAddressed in the full evidence report.
aSome studies were included for multiple key questions (KQs).
bAddressed in the full evidence report.
The area of each square represents each pooled estimate (subgroup or overall analysis), and the width of each diamond represents the confidence interval for the pooled estimate. The dashed line indicates the overall measure of effect. SVR indicates sustained virologic response.
The area of each square represents each pooled estimate (subgroup or overall analysis), and the width of each diamond represents the confidence interval for the pooled estimate. Dashed lines indicate the overall measures of effect; overall estimates were from mixed-effects models. DAA indicates direct-acting antiviral; IFN, interferon; NR, not reported; SVR, sustained virologic response.
eMethods 1. Literature Search Strategies
eMethods 2. Quality Assessment Criteria
eTable 1. Quality of Life and Functional Outcomes After Direct Acting Antiviral Therapy
eTable 2. Observational Studies of Direct Acting Antiviral Therapy on Health Outcomes in Adults
eTable 3. Trials of Direct Acting Antiviral Regimens and Quality of Life in Adolescents
eTable 4. Trials of Sustained Virologic Response With Direct Acting Antiviral Regimens in Adults
eTable 5. Quality Assessment of Studies of Direct Acting Antiviral Therapy in Adults
eTable 6. Sustained Virologic Response in Comparative Trials of Direct Acting Antiviral Regimens in Adults
eTable 7. Sustained Virologic Response Rates With Direct Acting Antiviral Regimens in Adults by Genotype
eTable 8. Sustained Virologic Response Rates With Direct Acting Antiviral Regimens in Adolescents With HCV Infection
eTable 9. Adverse Events of Direct Acting Antivirals Versus Placebo
eTable 10. Adverse Events of Direct Acting Antivirals Versus Other Drugs
eTable 11. Pooled Rates With Direct Acting Antiviral Regimens in Adults for Any Adverse Event, Serious Adverse Events, and Withdrawals due to Adverse Events
eTable 12. Pooled Rates With Direct Acting Antiviral Regimens in Adults for Anemia, Fatigue, Headache, and Insomnia
eTable 13. Pooled Rates With Direct Acting Antiviral Regimens in Adults for Nausea, Diarrhea, Vomiting, and Rash
eTable 14. Adverse Events With Direct Acting Antiviral Regimens in Adolescents
eTable 15. Studies on the Association Between Sustained Virologic Response After Antiviral Therapy Versus No Sustained Virologic Response and Clinical Outcomes
eTable 16. Pooled Estimates on the Association Between Sustained Virologic Response After Antiviral Therapy Versus No Sustained Virologic Response and Clinical Outcomes
eFigure 1. Direct Acting Antiviral Regimens and Pooled Sustained Virologic Response Rates, Genotype 2
eFigure 2. Direct Acting Antiviral Regimens and Pooled Sustained Virologic Response Rates, Genotype 3
eFigure 3. Direct Acting Antiviral Regimens and Sustained Virologic Response Rates, Genotype 4
eFigure 4. Direct Acting Antiviral Regimens and Pooled Rates for Any Adverse Event
eFigure 5. Direct Acting Antiviral Regimens and Pooled Rates for Serious Adverse Events
eFigure 6. Direct Acting Antiviral Regimens and Pooled Rates for Withdrawal Due to Adverse Events
eFigure 7. Association of Sustained Virologic Response With Liver Mortality
eFigure 8. Association of Sustained Virologic Response With Cirrhosis
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Chou R, Dana T, Fu R, et al. Screening for Hepatitis C Virus Infection in Adolescents and Adults: Updated Evidence Report and Systematic Review for the US Preventive Services Task Force. JAMA. 2020;323(10):976–991. doi:10.1001/jama.2019.20788
A 2013 review for the US Preventive Services Task Force (USPSTF) of hepatitis C virus (HCV) screening found interferon-based antiviral therapy associated with increased likelihood of sustained virologic response (SVR) and an association between achieving an SVR and improved clinical outcomes. New direct-acting antiviral (DAA) regimens are available.
To update the 2013 review on HCV screening to inform the USPSTF.
Ovid MEDLINE, the Cochrane Central Register of Controlled Trials, and the Cochrane Database of Systematic Reviews through February 2019, with surveillance through September 2019.
Randomized clinical trials (RCTs) and nonrandomized treatment studies of HCV screening and DAA therapy; cohort studies on screening, antiviral therapy, and the association between an SVR after antiviral therapy and clinical outcomes.
Data Extraction and Synthesis
One investigator abstracted data; a second checked accuracy. Two investigators independently rated study quality.
Main Outcomes and Measures
Mortality, morbidity, quality of life, screening and treatment harms, and screening diagnostic yield.
Eight RCTs of DAA therapy vs placebo or an outdated antiviral regimen, 48 other treatment studies, and 33 cohort studies, with a total of 179 230 participants, were included. No study evaluated effects of HCV screening vs no screening. One new study since the 2013 review (n = 5917) found similar diagnostic yield of risk-based screening (sensitivity, 82%; number needed to screen to identify 1 HCV case, 15) and birth cohort screening (sensitivity, 76%; number needed to screen, 29), assuming perfect implementation. Ten open-label studies (n = 3292) reported small improvements in some quality-of-life and functional outcomes (eg, less than 3 points on the 0 to 100 36-Item Short Form Health Survey physical and mental component summary scales) after DAA treatment compared with before treatment. Two cohort studies (n = 24 686) found inconsistent associations of antiviral therapy vs no therapy with risk of hepatocellular carcinoma. Forty-nine treatment studies (n = 10 181) found DAA regimens associated with pooled SVR rates greater than 95% across genotypes, and low short-term rates of serious adverse events (1.9%) and withdrawal due to adverse events (0.4%). An SVR after antiviral therapy was associated with decreased adjusted risk of all-cause mortality (13 studies, n = 36 986; pooled hazard ratio [HR], 0.40 [95% CI, 0.28-0.56) and hepatocellular carcinoma (20 studies, n = 84 491; pooled HR, 0.29 [95% CI, 0.23 to 0.38]) vs no SVR.
Conclusions and Relevance
Direct evidence on the effects of HCV screening on clinical outcomes remains unavailable, but DAA regimens were associated with SVR rates greater than 95% and few short-term harms relative to older antiviral therapies. An SVR after antiviral therapy was associated with improved clinical outcomes compared with no SVR.
It has been estimated that from 2013 to 2016 approximately 4.1 million people in the US were hepatitis C virus (HCV) antibody–positive, indicating past exposure, and that of these, approximately 2.4 million had active infection.1 Persons born between 1945 and 1965 were estimated to account for approximately three-fourths of HCV infections. However, recent increases in acute HCV incidence have mostly affected young persons who inject drugs.2,3
In 2013, the US Preventive Services Task Force (USPSTF) recommended HCV screening for adults born between 1945 and 1965 (“birth cohort” screening) and those at high risk of infection (B recommendation).4 The recommendation was based on the effectiveness of then-current antiviral therapies with interferon. HCV treatment has subsequently evolved to direct-acting antiviral (DAA) regimens without interferon.
This evidence report was conducted to update the 2013 USPSTF review on HCV screening in adults5,6 and a comparative effectiveness review on antiviral treatments,7,8 to inform the USPSTF for an updated recommendation statement. This report focused on currently recommended DAA regimens and was expanded to include adolescents.
Detailed methods and evidence tables with additional study details are available in the full evidence report at https://www.uspreventiveservicestaskforce.org/Page/Document/UpdateSummaryFinal/hepatitis-c-screening1. Figure 1 shows the analytic framework and key questions (KQs) that guided the review. KQs on prenatal HCV screening (KQ 1b) and interventions to prevent vertical HCV transmission during labor and delivery (KQ5) are addressed in the full report.
Ovid MEDLINE, the Cochrane Central Register of Controlled Trials, and the Cochrane Database of Systematic Reviews were searched from 2013 through February 2019 (eMethods 1 in the Supplement). Searches were supplemented by reference list review of relevant systematic reviews; studies from the prior USPSTF review6,9 meeting inclusion criteria were carried forward. Ongoing surveillance was conducted to identify major studies published since February 2019 that may affect the conclusions or understanding of the evidence and the related USPSTF recommendation. The last surveillance was conducted on September 20, 2019, and identified no studies affecting review conclusions.
Two investigators independently reviewed titles, abstracts, and full-text articles using predefined eligibility criteria. The population for screening was asymptomatic adults and adolescents without prior HCV infection. For treatment, to evaluate patients more likely to be asymptomatic and identified by screening, inclusion was restricted to studies in which 20% or less of patients had cirrhosis at baseline (≤30% for cohort studies that controlled for fibrosis stage). Randomized clinical trials (RCTs) of screening and currently recommended DAA regimens vs placebo or an outdated antiviral regimen10 were included. Because of few randomized trials of DAA therapy vs placebo or an outdated antiviral regimen, nonrandomized clinical research treatment studies of DAA therapy (including those with a single group) and randomized trials that compared different DAA regimens were also included. The latter were classified as nonrandomized treatment studies rather than randomized trials in this review because data from relevant DAA regimens were analyzed separately (ie, the randomized comparison was not used). Cohort studies that controlled for potential confounders were included for screening; for associations of antiviral therapy (including older regimens) with mortality, hepatocellular carcinoma, and cirrhosis; and for the association between SVR after antiviral therapy and clinical outcomes. Outcomes were mortality, morbidity (eg, cirrhosis, hepatic decompensation, liver transplant, extrahepatic manifestations of HCV infection), quality of life, HCV transmission, sustained virologic response (SVR), harms, and screening yield (sensitivity and number of new diagnoses per test performed). Studies that focused on persons co-infected with HIV or hepatitis B virus, patients receiving transplants, and persons with advanced kidney disease were excluded.
One investigator abstracted details about the study design, patient population, setting, interventions, analysis, follow-up, and results from each study. A second investigator reviewed abstracted data for accuracy. Two independent investigators assessed the quality of each study as good, fair, or poor using predefined criteria developed by the USPSTF (eMethods 2 in the Supplement).7 Discrepancies were resolved through a consensus process. In accordance with the USPSTF Procedure Manual,7 studies rated poor quality because of critical methodological limitations were excluded.
Random effects meta-analysis was performed to summarize the proportion of patients experiencing SVR and adverse events using a generalized linear mixed-effects model with a logit link. Analyses were stratified according to DAA regimen. For SVR, separate analyses were performed for each HCV genotype. A random-effects (linear mixed-effects) meta-analysis was also performed on adjusted hazard ratios (HRs) for SVR after antiviral therapy vs no SVR and for clinical outcomes (mortality, liver-related mortality, cirrhosis, and hepatocellular carcinoma). If necessary, the adjusted HR for SVR vs no SVR was calculated from the adjusted HRs for SVR and no SVR vs no treatment. Statistical heterogeneity was assessed using the I2 statistic.11
Subgroup analyses were conducted on geographic setting (US or Europe; multinational; other), fibrosis stage (cirrhosis excluded or some patients [up to 20%] with cirrhosis), prior treatment status (naive or experienced to interferon-based therapies, boceprevir, or telaprevir), quality, and for cohort studies, full adjustment for key confounding variables (age, sex, fibrosis stage, and genotype). Stratified analyses were assessed for interactions using a test for heterogeneity across subgroups. For the association between DAA therapy and SVR rates, sensitivity analysis was performed by excluding studies in which ribavirin or dasabuvir was not used as recommended. For the association between SVR vs no SVR after antiviral therapy and clinical outcomes, sensitivity analysis was performed by excluding cohort studies with potentially overlapping populations to ensure that results were not sensitive to double counting of patients. For analyses of harms, trials of ribavirin-containing regimens were excluded except for ombitasvir/paritaprevir/ritonavir/dasabuvir, which is recommended for genotype 1b infection.
Meta-analyses were conducted using SAS version 9.4 (SAS Institute Inc) and RevMan version 5.3.5 (Nordic Cochrane Centre), and forest plots were created using Stata/SE version 14.0 (StataCorp). All significance testing was 2-tailed; P < .05 was considered statistically significant.
Across all KQs addressed in this article, 8 (n = 3397) RCTs (in 6 publications),12-17 48 (n = 7132) nonrandomized treatment studies (in 45 publications),18-62 33 (n = 168 701) cohort studies,63-95 2 additional pooled analyses,96,97 and 1 retrospective study (n = 5917)98 on the yield of alternative screening strategies in a cohort of patients in a national survey were included (Figure 2). Eighty-three studies12-62,64,66-74,77,79,81-83,85-92,95-98 were new for this update, and 963,65,75,76,78,80,84,93,94 were carried forward from the previous USPSTF review.
Key Question 1a. Does screening for HCV infection in pregnant and nonpregnant adolescents and adults without known abnormal liver enzyme levels reduce HCV-related mortality and morbidity or affect quality of life?
No study met inclusion criteria for this KQ.
Key Question 2. What is the effectiveness of different risk- or prevalence-based methods for screening for HCV infection on clinical outcomes?
Key Question 3. What is the yield (number of new diagnoses per tests performed) of 1-time vs repeat screening or alternative screening strategies for HCV infection, and how does the screening yield vary in different risk groups?
A retrospective study (n = 5917) compared the yield of risk-based HCV screening vs birth cohort screening in a cohort of patients sampled from the National Health and Nutrition Examination Survey.98 It found that applying risk-based guidelines perfectly would screen 24.7% of the US general population and identify 82% of HCV cases, with a number needed to screen to identify 1 HCV case of 14.6. Applying the birth cohort strategy would screen 45% of the general population and identify 76% of cases, with a number needed to screen of 28.7. No study evaluated the yield of 1-time vs repeat screening, the yield of alternative screening strategies in different risk groups, or the yield of currently recommended screening vs expanded screening strategies.
Key Question 4. What are the harms of screening for HCV infection (eg, anxiety and labeling)?
No study compared harms of HCV screening vs no screening. Poor-quality evidence from the prior USPSTF review suggested potential negative psychological and social effects of screening but was uncontrolled and did not meet inclusion criteria for this update.
Key Question 6. What is the effectiveness of currently recommended antiviral treatments in improving health outcomes in patients with HCV infection?
Ten open-label treatment studies (n = 2404) reported quality-of-life and functional outcomes before and after receipt of current DAA regimens (eTable 1 in the Supplement). Seven studies were included in 2 pooled analyses,95,96 and there were 3 additional studies (reported in 2 publications).12,99
At 12 weeks after treatment, 2 pooled analyses found sofosbuvir/velpatasvir (4 trials) or sofosbuvir/ledispavir (3 trials) associated with improvements in some measures of quality of life or function compared with before treatment, though differences were small (eg, less than 3 points on the 36-Item Short Form Health Survey physical and mental component summary scales [range, 0-100 points] or 0.04 to 0.05 points on the 6-Dimensional Health State Form health utility scale), and not all differences were statistically significant.95,96 Results were similar in 2 studies of ombitasvir/paritaprevir/ritonavir/dasabuvir12 or elbasvir/grazoprevir.99
Thirty-one treatment studies (in 28 publications; n = 3848) reported mortality at 12 to 36 weeks after completion of DAA therapy but were not designed to assess this outcome.14-19,24,25,27,28,30-32,36,37,39,41-44,46,48,49,51-55 Twenty-one studies reported no deaths, and the remaining 10 studies reported 17 deaths (0.4% overall. Ten deaths occurred in 3 studies of persons reporting recent injection drug use or use of opioid substitution therapy.31,32,55
Three cohort studies (n = 58 892) evaluated other clinical outcomes (eTable 2 in the Supplement).67,68,83 Follow-up ranged from 1.1 to 7.4 years. One study found DAA therapy, vs interferon-based therapy or antiviral therapy, was associated with decreased risk of cardiovascular events, including acute myocardial infarction, congestive heart failure, and stroke (incidence rate per 1000 person-years of follow-up, 16.3 [95% CI, 14.7 to 18.0] for DAA therapy; 23.5 [95% CI, 21.8 to 25.3] for interferon-based therapy; and 30.4 [95% CI, 29.2 to 31.7] for no therapy; P < .001 for antiviral therapy vs no therapy).67 One study found DAA and interferon-based therapy associated with similar incidence of hepatocellular carcinoma that was lower than with no antiviral therapy (incidence rate per 1000 person-years, 7.5 [95% CI, 6.5 to 8.6] and 7.9 [95% CI, 6.0 to 10.4] for antiviral therapy and 10.9 [95% CI, 9.92 to 11.97] for no therapy; P value not reported).83 The third study found no difference between DAA therapy vs no antiviral therapy in risk of hepatocellular carcinoma (adjusted HR, 1.02 [95% CI, 0.40 to 2.61]); point estimates for associations with all-cause mortality favored DAA therapy, but the difference was not statistically significant (adjusted HR, 0.74 [95% CI, 0.43 to 1.28]).68
Three treatment studies of adolescents (n = 200) reported changes of 2 to 13 points on Pediatric Quality of Life Inventory (scale, 0-100) scores after treatment with DAA therapy compared with baseline; effects were not always statistically significant (eTable 3 in the Supplement).59,61,100 Treatment studies of DAA therapy in adolescents were not designed to evaluate mortality (no deaths in 3 studies)57,61,62 or long-term clinical outcomes.
Key Question 7. What is the effectiveness of currently recommended antiviral treatments in achieving an SVR in patients with HCV infection?
Forty-nine studies (in 44 publications; n = 10 181) reported effects of current DAA treatment regimens on SVR in patients with HCV infection.12-55 SVR was measured 12 weeks after the completion of therapy in all studies except for 1, which measured SVR at 14 weeks. Sample sizes ranged from 20 to 706, mean age ranged from 45 to 68 years, and the proportion of women ranged from 18% to 64%; the studies evaluated 7 different antiviral regimens (eTable 4 in the Supplement). One study was a randomized trial that compared a current DAA regimen vs placebo,14 2 randomized trials (reported in 1 publication) compared a current DAA regimen vs a regimen with telaprevir,12 and 2 randomized trials (reported in 1 publication) compared a current vs older DAA regimen.15 The other treatment studies did not compare a current DAA regimen vs placebo or an older regimen.
Thirteen studies were rated as good quality12-14,17,19,28,29,33,35,36,46,51,54 and the remainder as fair quality (eTable 5 in the Supplement). Methodological limitations included unclear randomization or enrollment methods. Loss to follow-up was low (range, 0%-3%). All of the trials were industry-funded.
Few studies compared DAA interventions with placebo or older interventions (eTable 5 in the Supplement). One randomized trial found sofosbuvir/velpatasvir associated with very high likelihood of SVR vs placebo in persons with mixed-genotype (1, 2, 4, 5, or 6) infection (99% vs 0%; relative risk [RR], 231.6 [95% CI, 14.6 to 3680]).14 Two randomized trials found ombitasvir/paritaprevir/ritonavir/dasabuvir (with or without ribavirin) associated with increased likelihood of SVR vs telaprevir/pegylated interferon/ribavirin in treatment-naive persons with genotype 1 infection (98% vs 80%; RR, 1.22 [95% CI, 1.08 to 1.37]) or persons previously treated with interferon therapy (99% vs 66%; RR, 1.50 [95% CI, 1.22 to 1.85]).12 Two randomized trials found sofosbuvir/velpatasvir for 12 weeks associated with increased likelihood of SVR vs sofosbuvir/ribavirin for 24 weeks for genotype 2 (99% vs 94%; RR, 1.06 [95% CI, 1.01 to 1.11]) and for genotype 3 infection (noncirrhosis subgroup, 97% vs 87%; RR, 1.11 [95% CI, 1.05 to 1.18]).15
For genotype 1 HCV infection, the most common genotype in the US, DAA therapy was associated with a pooled SVR rate of 97.7% (95% CI, 96.6% to 98.4%; I2 = 82%) based on 32 studies (n = 6055) (Figure 3). Evidence for genotypes 2 through 6 was more limited, ranging from 75 to 742 participants per genotype (eTable 7 in the Supplement). The pooled SVR rates ranged from 95.5% to 98.9%; for other common US genotypes, the pooled SVR was 98.9% (95% CI, 97.5% to 99.5%; I2 = 4%) for genotype 2 (5 studies, n = 526) (eFigure 1 in the Supplement), 95.5% (95% CI, 91.6% to 97.7%; I2 = 66%) for genotype 3 (6 studies, n = 742) (eFigure 2 in the Supplement), and 98.2% (95% CI, 94.7% to 99.4%; I2 = 50%) for genotype 4 (10 studies, n = 485) (eFigure 3 in the Supplement). Across genotypes, SVR estimates were consistent when studies were stratified according to study quality, geographic setting, prior HCV treatment, inclusion of some patients with cirrhosis at baseline, and use of ribavirin as recommended (eTable 7 in the Supplement).
Seven studies (n = 348) evaluated the effects of DAA regimens on SVR in adolescents (eTable 8 in the Supplement).56-62 Mean age ranged from 12 to 15 years, and the proportion of female participants ranged from 35% to 66%. Three of the 7 studies were conducted in Egypt and focused on genotype 4 infection, 1 study enrolled patients with genotype 1, and 3 studies enrolled mixed genotypes. Four studies evaluated DAA regimens approved by the US Food and Drug Administration (FDA) for use in adolescents,57-59,61 and the others evaluated DAA regimens recommended for adults but not FDA-approved for adolescents.56,60,62 Across all intervention studies of DAA in adolescents, the SVR rate ranged from 97% to 100%.
Key Question 8. What are the harms of currently recommended antiviral treatments?
Forty-nine treatment studies (in 44 publications; n = 10 181) of DAA regimens without interferon reported the proportion of patients who experienced adverse events at short-term follow-up (ie, while taking antiviral therapy through up to 12 weeks after completion of therapy).12-55
Four randomized trials (total n = 2113) reported adverse events associated with current DAA regimens vs placebo (eTable 9 in the Supplement).13,14,16,17 DAA regimens were associated with slightly increased risk of any adverse event (4 trials; RR, 1.12 [95% CI, 1.02 to 1.24]; I2 = 46%; absolute risk difference [ARD], 8% [95% CI, 8% to 15%]) (eTable 9 in the Supplement). DAA therapy was also associated with increased risk of nausea (3 trials; RR, 1.42 [95% CI, 1.00 to 2.03]; I2 = 10%; ARD, 4% [95% CI, −3% to 10%]); the association with increased risk of diarrhea was not statistically significant (2 trials; RR, 1.53 [95% CI, 0.88 to 2.68]; I2 = 29%). There were no differences between DAA regimens vs placebo in risk of serious adverse events, withdrawal due to adverse events, headache, or fatigue.
Two randomized trials (reported in 1 publication; n = 457) compared a DAA regimen (ombitasvir/paritaprevir/ritonavir/dasabuvir with or without ribavirin) vs telaprevir/pegylated interferon/ribavirin for genotype 1 infection (eTable 10 in the Supplement).12 DAA therapy was associated with decreased risk of serious adverse events (RR, 0.08 [95% CI, 0.02 to 0.34]; I2 = 0%; ARD, −8% [95% CI, −15% to −1%]) and withdrawal due to adverse events (RR, 0.06 [95% CI, 0.01 to 0.29]; I2 = 0%; ARD, −9% [95% CI, −14% to −3%]) vs the telaprevir regimen. DAA therapy was also associated with decreased risk of fatigue, headache, nausea, anemia, and rash (eTable 10 in the Supplement).
DAA therapy was frequently associated with experiencing any adverse event (44 trials, n = 8045; 73.3% [95% CI, 68.0% to 78.1%]; I2 = 95%) (eFigure 4 in the Supplement), though serious adverse events (44 studies, n = 8070; 1.9% [95% CI, 1.5% to 2.4%]; I2 = 33%) (eFigure 5 in the Supplement) and withdrawal due to adverse events (44 studies, n = 8060; 0.4% [95% CI, 0.3% to 0.6%]; I2 = 0%) (eFigure 6 in the Supplement) were infrequent (eTable 11 in the Supplement). Pooled rates for specific adverse events ranged from 2.4% (anemia) to 18.7% (headache) (eTables 12 and 13 in the Supplement). There was some variability by DAA regimen in estimates of adverse events; estimates were generally higher for ombitasvir/paritaprevir/ritonavir/dasabuvir with ribavirin than without ribavirin (eTables 11-13 in the Supplement). Adverse event estimates were generally similar when studies were stratified according to baseline cirrhosis status and prior antiviral therapy experience.
Seven treatment studies (n = 348) of DAA regimens in adolescents reported harms, but methods for reporting and assessing harms were generally not well described (eTable 14 in the Supplement).56-62 Rates of any adverse event were 27% in 1 study62 and ranged from 71% to 87% in 4 studies.57,59-61 There were no withdrawals due to adverse events reported in 5 studies,57,59-62 and 1 study61 reported 1 serious adverse event (a grade 3 joint injury). Rates of other adverse events were highly variable. For example, 3% to 48% of study participants reported headache. Stratification according to DAA regimen did not explain the observed variability.
Key Question 9. What is the association between experiencing SVR following antiviral treatment and reduction in risk of HCV-related adverse health outcomes?
Thirty cohort studies reported associations between achieving SVR after antiviral treatment vs no SVR and clinical outcomes (eTable 15 in the Supplement).63-66,68-82,84-94 Sample sizes ranged from 131 to 50 886 (total n = 116 659), mean age ranged from 42 to 69 years, and the proportion of women ranged from 1% to 56%. Seventeen studies were conducted in Japan (including some with overlapping populations),63,64,71,73-75,78-81,84-86,89,90,92,93 4 in other Asian countries,82,88,91,94 7 in the US (all except for 187 conducted in Veterans Affairs populations),65,66,69,70,72,77,87 and 2 in Europe.68,76 When genotype was reported, genotype 1 was generally the most common (36%-89%) and genotype 2 the second most common (6%-52%). Mean follow-up ranged from 1.5 to 10 years in all studies except for 1 study that described follow-up of at least 1 year.88 Twenty-six studies evaluated interferon-based therapies. Three studies focused on DAAs,66,68,77 1 study evaluated interferon-based treatments and DAAs,77 and 1 study did not report what type of treatment was administered (likely primarily interferon-based therapies).72 All studies were rated fair quality (eTable 16 in the Supplement).
SVR was associated with significantly decreased risk of all-cause mortality (13 studies, n = 36 986; HR, 0.40 [95% CI, 0.28 to 0.56]; I2 = 52%) (Figure 4).63,65,66,68-70,75,76,80,84,87,93,94 Studies with longer duration of follow-up (>5 years) reported a stronger association between SVR after antiviral therapy and reduced risk of all-cause mortality (pooled HR, 0.33 [95% CI, 0.24 to 0.46]) than those with shorter follow-up (pooled HR, 0.64 [95% CI, 0.56 to 0.74]) (P = .003 for interaction). SVR was also associated with decreased risk of hepatocellular carcinoma (20 studies, n = 84 491; pooled HR, 0.29 [95% CI, 0.23 to 0.38]; I2 = 19%) (Figure 4),63,64,68,70-74,77-79,81,82,84-86,89,90,92,94 liver-related mortality (4 studies, n = 5953; pooled HR, 0.11 [95% CI, 0.04 to 0.27]; I2 = 0%) (eFigure 7 in the Supplement),63,75,80,93 and cirrhosis (4 cohorts reported in 3 studies, n = 16 735; pooled HR, 0.36 [95% CI, 0.33 to 0.40]; I2 = 0%) (eFigure 8 in the Supplement).69,72,91 There were no statistically significant interactions when studies were stratified according to how well they adjusted for key confounders, duration of follow-up, country/setting, or the proportion of participants with cirrhosis at baseline (eTable 15 in the Supplement). Results were also similar when studies with potentially overlapping populations were excluded.
The findings in this evidence report are summarized in the Table. Since the prior USPSTF recommendation, there has been a major shift in antiviral therapy to all-oral DAA regimens without interferon. New pooled evidence indicates that SVR rates with currently recommended all-oral DAA regimens are substantially higher (>95%) than with interferon-based therapies evaluated in the prior review (68%-78%).9 Although statistical heterogeneity was present in pooled estimates of SVR rates, findings were robust when studies were stratified according to the DAA regimen evaluated, study quality, prior treatment status, and cirrhosis status. Few randomized trials directly compared a current DAA regimen vs placebo or an older antiviral regimen, but those available also found DAA therapy associated with greater effectiveness. DAA regimens were associated with fewer harms than older interferon-containing therapies. Evidence on DAA therapies in adolescents was limited, but consistently reported high (97%-100%) SVR rates.
Direct evidence on the effects of antiviral therapy on clinical outcomes is limited. Although several randomized trials found interferon therapy associated with decreased risk of hepatocellular carcinoma compared with no antiviral therapy, they did not meet inclusion criteria for this report because they focused on patients with cirrhosis at baseline or used a nonstandard regimen.101-108 Studies of DAA therapies were not designed to assess effects on mortality or other long-term clinical outcomes. There were few cohort studies of antiviral therapy vs no therapy, results were somewhat inconsistent, and findings were susceptible to residual confounding. Given the limited direct evidence on the effects of antiviral therapy on clinical outcomes, cohort studies of the association between SVR after antiviral therapy vs no SVR and clinical outcomes may help to understand potential clinical effects of DAA therapy. As in the prior USPSTF review, there was a consistent association between SVR after antiviral therapy and improved clinical outcomes, including mortality and hepatocellular carcinoma.9
The findings in this evidence report regarding the benefits and harms of current DAA regimens were consistent with a recent systematic review that also reported high (>95%) SVR rates in genotype 1 infection without cirrhosis, high SVR rates but more limited evidence for other HCV genotypes, low rates of serious adverse events and treatment discontinuation, and higher adverse event rates with ribavirin.109 The results are also consistent with a systematic review that found insufficient evidence from clinical trials to determine effects of DAA regimens on HCV-related mortality and morbidity110; unlike that review, this one also evaluated the indirect chain of evidence linking DAA therapy with SVR, and SVR with clinical outcomes. This review is consistent with prior reviews that found a consistent association between an SVR after antiviral therapy and reduced risk of mortality and hepatocellular carcinoma.111-113
Research is needed to better understand the association between use of current DAA therapy and clinical outcomes. Long-term randomized trials of treatment vs no treatment would be ethically challenging and difficult to carry out. Alternatively, large cohort studies that measure important confounders could be highly informative. Trials and cohort studies that measure effects on quality of life, function, and extrahepatic effects of HCV infection would also be helpful for understanding effects of DAA regimens on these shorter-term clinical outcomes. Studies on the association between SVR after DAA therapy and clinical outcomes would help to verify the link between SVR and clinical outcomes with current DAA therapies. Additional studies would be helpful for confirming the effectiveness of DAA regimens in adolescents, including long-term outcomes.114 Well-designed prospective studies are needed to understand the effects of different HCV screening strategies, including repeat screening, on diagnostic yield.
This review has several limitations. First, because there were few randomized trials of current DAA regimens, nonrandomized treatment studies were included, among which were studies without a non-DAA therapy comparison group. Causality cannot be concluded from such studies. Nonetheless, such studies were considered highly informative for SVR, an objective measure with rates without treatment close to zero. However, more subjective outcomes such as quality of life, function, and adverse events are more difficult to interpret in the absence of randomization or a comparison group. Second, no study of DAA therapy was conducted in screen-detected patients, and few studies reported presence or severity of baseline symptoms. Therefore, to evaluate effectiveness of DAA therapies in populations likely to be identified by screening, this report selected studies based on proxy factors, specifically a low prevalence of cirrhosis and prior DAA experience. Research studies of DAA therapy could overestimate SVR rates compared with typical clinical practice. However, observational studies reported SVR rates of 90%, only modestly lower than observed in the trials.115,116
Third, some studies of DAA therapy in adolescents evaluated regimens approved for adults but not children. Fourth, evidence on potential long-term harms of DAA therapy exposure was limited. However, limited evidence indicates no increased risk of hepatocellular carcinoma with DAA therapy compared with interferon-based therapy through around 3 years of follow-up.68
Fifth, non–English-language articles were excluded. Sixth, formal assessment for small sample effects (a potential marker of publication bias) using graphical or statistical methods was not performed because of the small number of randomized trials.
Direct evidence on the effects of HCV screening on clinical outcomes remains unavailable, but all-oral DAA regimens were associated with SVR rates greater than 95% and few short-term harms relative to older antiviral therapies. An SVR after antiviral therapy was associated with improved clinical outcomes compared with no SVR.
Corresponding Author: Roger Chou, MD, Oregon Health & Science University, 3181 SW Sam Jackson Park Rd, Mail Code BICC, Portland, OR 97239 (email@example.com).
Accepted for Publication: December 3, 2019.
Published Online: March 2, 2020. doi:10.1001/jama.2019.20788
Correction: This article was corrected online on March 10, 2020, for incorrect data in the abstract Conclusions, incorrect presentation in Figure 1, and incorrect data in Figure 3.
Author Contributions: Dr Chou had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Concept and design: Chou, Wagner, Jou.
Acquisition, analysis, or interpretation of data: All authors.
Drafting of the manuscript: Chou, Dana, Fu, Wagner, Ramirez, Grusing.
Critical revision of the manuscript for important intellectual content: Chou, Zakher, Jou.
Statistical analysis: Chou, Dana, Fu.
Obtained funding: Chou.
Administrative, technical, or material support: Dana, Wagner, Grusing.
Supervision: Chou, Wagner, Jou.
Conflict of Interest Disclosures: Dr Chou reported receiving personal fees from the World Health Organization. Dr Fu reported receiving grants from Oregon Health & Science University. No other disclosures were reported.
Funding/Support: This research was funded under contract HHSA290201500009i, Task Order 7, from the Agency for Healthcare Research and Quality (AHRQ), US Department of Health and Human Services, under a contract to support the US Preventive Services Task Force (USPSTF).
Role of the Funder/Sponsor: Investigators worked with USPSTF members and AHRQ staff to develop the scope, analytic framework, and key questions for this review. AHRQ had no role in study selection, quality assessment, or synthesis. AHRQ staff provided project oversight, reviewed the report to ensure that the analysis met methodological standards, and distributed the draft for peer review. Otherwise, AHRQ had no role in the conduct of the study; collection, management, analysis, and interpretation of the data; and preparation, review, or approval of the manuscript findings. The opinions expressed in this document are those of the authors and do not reflect the official position of AHRQ or the US Department of Health and Human Services.
Additional Contributions: We thank the AHRQ Medical Officer (Iris Mabry-Hernandez, MD). We also acknowledge past and current USPSTF members who contributed to topic deliberations. The USPSTF members, external reviewers, and federal partner reviewers did not receive financial compensation for their contributions.
Additional Information: A draft version of this evidence report underwent external peer review from 6 content experts (Michael F. Chang, MD, Oregon Health & Science University; Oluwaseun Falade-Nwulia, MBBS, Johns Hopkins University; Yngve Falck-Ytter, MD, Louis Stokes VA Cleveland Medical Center; Brenna L. Hughes, MD, Duke University; Karla Thornton, MD, University of New Mexico; and John W. Ward, MD, Task Force for Global Health Inc) and 3 federal partners representing the Centers for Disease Control and Prevention and 1 federal partner representing the National Institutes of Health, National Institute of Allergy and Infectious Diseases. None of the reviewers received compensation for their role in reviewing the report. Comments from reviewers were presented to the USPSTF during its deliberation of the evidence and were considered in preparing the final evidence review.
Editorial Disclaimer: This evidence report is presented as a document in support of the accompanying USPSTF Recommendation Statement. It did not undergo additional peer review after submission to JAMA.
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