Publish in this journal
Journal Information
Download PDF
More article options
Original article
DOI: 10.1016/j.bjid.2018.04.003
Effectiveness and tolerability of direct-acting antivirals for chronic hepatitis C patients in a Southern state of Brazil
Vinicius Lins Ferreiraa, Helena Hiemisch Lobo Borbaa, Astrid Wiensa, Maria Lucia Alves Pedrosob, Vanessa Ferreira de Camargo Radunzb, Cláudia Alexandra Pontes Ivantesc, Aline Satie Oba Kuniyoshid, Roberto Pontaroloa,
Corresponding author

Corresponding author.
a Universidade Federal do Paraná, Programa de Pós-Graduação em Ciências Farmacêuticas, Curitiba, PR, Brazil
b Universidade Federal do Paraná, Hospital de Clínicas, Serviço de Gastroenterologia, Curitiba, PR, Brazil
c Gastroenterology Service, Centro de Orientação e Aconselhamento da Secretaria Municipal de Saúde, Curitiba, PR, Brazil
d Prefeitura de Maringá, Atendimento Especializado, Maringá, PR, Brazil
This item has received
Received 23 January 2018, Accepted 04 April 2018
Article information
Full Text
Download PDF
Tables (3)
Table 1. Baseline demographic and clinical characteristics.
Table 2. Analysis of sustained virological response (SVR) and comparison of patients treated with sofosbuvir and daclatasvir versus sofosbuvir and simeprevir.
Table 3. Response rates for patients treated with other DAA options.
Show moreShow less

This study aimed to evaluate the clinical effectiveness in terms of sustained virological response and tolerability of available second generation direct-acting antivirals in Brazilian patients.


This was a retrospective observational study conducted in six centers in Southern Brazil. The sample comprised adult patients who were chronically infected with hepatitis C virus, regardless of virus genotype, fibrosis stage, or prior treatment. Statistical analysis was performed to compare the effectiveness among the treatments, and also to uncover the factors influencing the achievement of sustained virological response.


A total of 296 patients were included in the study, with the majority receiving sofosbuvir with daclatasvir (59%) or sofosbuvir with simeprevir (26%). Overall sustained virological response rates were approximately 91.6%. For genotype 1, sofosbuvir with daclatasvir had an sustained virological response rate of approximately 95%, while the sustained virological response rate of sofosbuvir with simeprevir was 92%; this difference was statistically significant only for subtype 1b. The only treatment used for genotype 3 patients was sofosbuvir with daclatasvir, and lower rates of sustained virological response were observed for this group, compared to genotype 1 (84% versus 95%, p<0.05). Apart from this difference between genotypes, and a difference between patients who achieved rapid virologic response compared with those who did not, there were no other statistically significant factors associated with sustained virological response.


The results point to the effectiveness of second-generation direct-acting antivirals in hepatitis C virus Brazilian patients, especially those with genotype 1. Furthermore, that patients with genotype 3 need more attention and adjustments in available treatment options.

Direct-acting antivirals
Hepatitis C
Observational study
Full Text

Chronic hepatitis C is a serious health-related problem that affects more than 71 million people, causing almost 400,000 deaths worldwide every year.1 In Brazil, it is estimated that 1.5–1.7 million patients are infected with the hepatitis C virus (HCV), which represents about 2% of the population. However, a higher proportion of cases is from the South of Brazil (about 24.2% of the total number of cases in the country), where Curitiba city, the capital of Paraná state, is one of cities with the highest number of cases per 100,000 inhabitants (36.3).2–4 For many years, interferon-based therapies were the primary treatment choice for chronic hepatitis C, followed by the first generation of direct-acting antivirals (DAAs), boceprevir and telapravir, which were used in combination with pegylated interferon and ribavirin (RBV). However, these treatments were problematic due to limited efficacy, severe side effects, and contraindications.5,6

In the last few years, second generation DAAs have been developed to provide more effective, tolerable, and safe treatments for hepatitis C. These can be used in combination with other second generation DAAs, and without interferon.7–11 Since 2015 three DAA options have been available in the Brazilian public health system: sofosbuvir, daclatasvir, and simeprevir. The Brazilian government makes these drugs available at no cost, according to national guidelines for treating chronic hepatitis C, which prioritize patients with advanced stage of the disease. Recently, another combination of drugs was approved for use in Brazil, i.e., ombitasvir with paritaprevir/ritonavir and dasabuvir.4

These combinations of drugs have shown high rates of sustained virological response (SVR; a primary efficacy outcome measured at least 12 weeks after the end of treatment) and a favorable tolerability profile in randomized clinical trials (RCTs) and previous systematic reviews.12–14 It is expected that these outcomes would also be reproduced in clinical practice.

Observational and regional studies are needed for evidence to support decisions in clinical practice. It is well established that this type of study is an important step in investigating clinical outcomes for chronic diseases, especially because, in some situations, results from RCTs are not fully representative of the general population.15,16 Hepatitis C is a disease which is associated with many factors that can complicate medical treatment. This includes HCV genotype, co-infections with other viruses (such as the human immunodeficiency virus, HIV), and patient conditions (e.g., cirrhosis, liver transplantation, renal failure). Geographical differences in the populations studied can also affect treatment response due to varied viral characteristics of patients; this may occur in Brazil, which is a country with considerable extension and regional diversities.

In this context, the study aimed to evaluate the clinical effectiveness, in terms of SVR, and tolerability of second generation DAAs in chronic hepatitis C patients through an observational cohort study conducted in a Southern state of Brazil. We also aimed to compare the results obtained from patients receiving sofosbuvir with daclatasvir versus sofosbuvir with simeprevir.

Materials and methodsStudy design, eligibility criteria, and treatment outcomes

In this retrospective observational study, we analyzed data from chronic hepatitis C patients who were treated in six centers in the South of Brazil, located in five different cities of the State of Paraná: Curitiba, Londrina, Cascavel, Ponta Grossa, and Maringá. The study was carried out in accordance with the ethical principles of the Declaration of Helsinki and was approved by the local Ethics Committee on Human Research.

Data were collected from databases from each center, which contain all the individual patient records. The sample comprised adult patients (≥18 years) diagnosed with chronic HCV infection who concluded or discontinued any second generation DAA treatment before April 2017. Patients were included regardless of genotype, prior treatment, or liver fibrosis stage. The choice, administration, and management of each patient's treatment was the responsibility of the centers, according to the national guidelines.4

The primary effectiveness outcome was SVR 12 weeks or more after the end of treatment (SVR12), which is defined as undetectable HCV by polymerase chain reaction (PCR). Secondary effectiveness outcomes included rapid virological response (RVR; defined as undetectable HCV RNA after four weeks of therapy) and end of treatment response (EOTr; defined as undetectable HCV RNA at treatment completion), both measured using PCR tests. Patients that completed therapy but did not have any SVR results (i.e., missing data or lost to follow up) were excluded from the analysis.

Clinical information collected at baseline included age, sex, weight, presence/absence of cirrhosis, prior treatment information, HCV genotype, viral load, liver biopsy information, intended treatment, comorbidities (hepatitis B, HIV), other clinical information (prior transplantation or hepatocarcinoma), and treatment discontinuation due to adverse events (tolerability outcome).

Statistical analysis

Baseline categorical variables are described as absolute and relative frequencies, while continuous variables are reported as medians and standard deviations. Analysis was carried out using the chi-square test and logistic regression to identify variables significantly associated with SVR (e.g., baseline parameters: treatment option, duration, sex, age, cirrhosis, prior treatment, and others). Bivariate logistic regression results are presented as odds ratios (OR) and their 95% confidence intervals (CI). A p-value less than 0.05 was considered statistically significant in all cases. Analysis was performed using SPSS Statistics version 24 (IBM SPSS, Chicago, IL, USA) and StatSoft Statistica version 10.

ResultsBaseline characteristics

In the six centers, 363 patients were retrieved for this observational study, although 61 were excluded due to lost follow-up and another six due to missing data (e.g., no treatment information). Data from 296 patients were used for per protocol analysis. The mean age of the participants was 57.8±10.8 years and 56% of the sample were males. In terms of treatment, 59% of patients were treated with sofosbuvir plus daclatasvir, 26% received sofosbuvir plus simeprevir, and 15% received other DAA therapy options. In total, 34% of patients received ribavirin together with the DAA treatment. Genotypes 1 (GT1; 66%) and 3 (GT3; 27%) were the most frequent genotypes observed, and 48% of the patients were treatment experienced. Baseline characteristics of patients that received the two most prevalent treatments (n=255), sofosbuvir with daclatasvir, and sofosbuvir with simeprevir, are shown in Table 1.

Table 1.

Baseline demographic and clinical characteristics.

Characteristic  SOF+DCV±RBV (n=176)  SOF+SMV±RBV (n=79)  Total (n=255) 
Male, n (%)  103 (58.5%)  38 (48.1%)a  141 (55.2%)a 
Mean (SD) age, years  58.1 (±10.3)  57.1 (±12.4)  57.8 (±10.8) 
HCV genotype
1 total  102 (57.9%)  79 (100.0%)  198 (66.8%) 
1 unspecified  26 (14.7%)  8 (10.1%)  34 (13.3%) 
1a  36 (20.4%)  39 (49.3%)  75 (29.4%) 
1b  40 (22.7%)  31 (39.2%)  71 (27.8%) 
72 (41.0%)  –  72 (28.2%) 
Missing data  2 (1.1%)  1 (1.2%)  3 (1.1%) 
Viral load800,000IUmL−1, n (%)  89 (50.5%)  37 (46.8%)  126 (49.4%) 
Missing data  9 (5.1%)  2 (2.5%)  11 (4.3%) 
Treatment experience, n (%)  92 (52.2%)  35 (44.3%)  127 (49.8%) 
Missing data  1 (0.5%)  3 (3.7%)  4 (1.5%) 
Fibrosis stage, n (%)
F0–F3  38 (21.5%)  32 (40.5%)  70 (27.4%)b 
F4 (cirrhotic)  77 (43.7%)  22 (27.8%)  99 (38.8%)b 
Missing data  61 (34.6%)  25 (31.6%)  86 (33.7%) 
Liver transplantation  5 (2.8%)  3 (3.7%)  8 (3.1%) 
Treatment duration, n (%)
12 weeks  129 (73.0%)a  77 (97.4%)  206 (80.7%)a,b 
24 weeks  44 (25.0%)  2 (2.5%)  46 (18.0%)b 
Addition of RBV, n (%)  56 (31.8%)  8 (10.1%)  64 (25.0%) 
Hepatitis B virus (HBV)  4 (2.2%)  1 (1.2%)  5 (1.9%) 
Human immunodeficiency virus (HIV)  10 (5.6%)  –  10 (13.9%) 

1 patient missing data.


p<0.05 (comparison between number of patients in each group that received sofosbuvir with daclatasvir versus sofosbuvir with simeprevir). Abbreviations: DAA, direct acting antivirals; DCV, daclatasvir; IFN, interferon; HCV, hepatitis C virus; LED, ledipasvir; RBV, ribavirin; SD, standard deviation; SMV, simeprevir; SOF, sofosbuvir.

Sub-cohort analysis of patients receiving sofosbuvir with daclatasvir

SVR was achieved by 160 patients (90%) of the 176 patients who were treated with sofosbuvir and daclatasvir (Fig. 1A and Table 2). This treatment was recommended for patients with GT 1 and 3; GT3 had lower SVR rates compared to patients infected with GT1 (95% versus 84%, p<0.05). All GT3 patients treated for 24 weeks achieved treatment response, compared to only 85% of GT3 patients treated for 12 weeks achieved SVR (although in this case p>0.05, more details in Supplementary Material 1). However, there was no statistically significant difference (p>0.05) in SVR rates in any of the other sub-analysis, including the use of sofosbuvir and daclatasvir with or without ribavirin (94% versus 88%), presence or absence of cirrhosis (92% versus 89%), prior treatment (95% versus 86%, respectively for treatment naïve and experienced patients), and treatment duration (95% versus 89%, respectively for 24 and 12 weeks of treatment).

Fig. 1.

Sustained virological response rates (SVR) for treatment with (A) sofosbuvir and daclatasvir; and (B) sofosbuvir and simeprevir: overall results, and rates according to clinical characteristics. Abbreviations: GT, genotype; RBV, ribavirin.

Table 2.

Analysis of sustained virological response (SVR) and comparison of patients treated with sofosbuvir and daclatasvir versus sofosbuvir and simeprevir.

  SOF+DCV±RBV, % (n=176)  SOF+SMV±RBV, % (n=79)  p-Value a 
Overall SVR %  90.9 (160/176)  92.4 (73/79)  0.69 
1 unspecified  92.3 (24/26)  87.5 (7/8)  0.67 
1a  91.6 (33/36)  94.8 (37/39)  0.57 
1b  100 (40/40)  90.3 (28/31)  0.04 
GT1 total  95.0 (97/102)  92.4 (73/79)  0.45 
84.7 (61/72)  –  NA 
Cirrhosis yes  92.2 (71/77)  90.9 (20/22)  0.84 
Cirrhosis no  89.4 (34/38)  93.7 (30/32)  0.52 
Cirrhosis NI  90.1 (55/61)  92.0 (23/25)  0.79 
Treatment naïve  95.1 (79/83)  97.5 (40/41)  0.52 
Treatment experienced  86.9 (80/92)  85.7 (30/35)  0.85 
Treatment 12 weeks  89.1(115/129)  93.5 (72/77)  0.29 
Treatment 24 weeks  95.4 (42/44)  50.0 (1/2)  0.01 
With RBV  94.6 (53/56)  87.5 (7/8)  0.50 
Without RBV  88.4 (100/113)  94.0 (63/67)  0.21 
Viral load
≥ 800.000IUmL−1  89.8 (80/89)  91.8 (34/37)  0.72 
<800.000IUmL−1  93.5 (73/78)  92.5 (37/40)  0.82 

Note: Some groups have different number of patients compared to total number of patients as it occurred missing data in some baseline parameters presented in Table 1.


Comparison between SOF+DCV±RBV versus SOF+SMV±RBV patients for each group Abbreviations: DAC, daclatasvir; GT, genotype; NA, not applicable; NI, not informed; RBV, ribavirin SOF, sofosbuvir; SMV, simeprevir.

RVR was obtained by 74 of 78 patients (94%), while EOTr was achieved by 90% (64 of 71). More detail regarding secondary outcomes is available in Supplementary Material 3.

Sub-cohort analysis of patients receiving sofosbuvir with simeprevir

Of the 79 patients that received sofosbuvir with simeprevir, 73 (92%) achieved SVR (Fig. 1B and Table 2). This DAA combination was only administered to HCV GT 1 patients; SVR rate was 94% for subtype 1a, 90% for subtype 1b, and 87% for unspecified GT 1 subtype. Other sub-analysis included prior treatment (97% versus 85% for treatment naïve and experienced patients). Use or non-use of ribavirin (87% versus 94%), and presence or absence of cirrhosis (90% versus 93%). There were no statistically significant differences (p>0.05), except for treatment duration (93% versus 50%, respectively for 12 and 24 weeks of treatment); however, this finding should be interpreted with caution as only two patients received treatment for 24 weeks.

RVR was achieved by 42 of 47 patients (89%), while EOTr was obtained by 100% of the patients where data was available (19 of 19). More detail regarding secondary outcomes is available in Supplementary Material 3.

Comparative effectiveness of sofosbuvir with daclatasvir versus sofosbuvir with simeprevir

Overall SVR rates were similar for both treatments (Table 2). For GT 1, sofosbuvir with daclatasvir had an SVR rate of 95%, compared to 92% for sofosbuvir with simeprevir (p>0.05), however, for GT 1b, sofosbuvir with daclatasvir was more effective (p<0.05). No statistically significant differences between therapies were observed in terms of prior treatment, cirrhosis (Supplementary Material 2 presents more details about SVR regarding genotype and presence/absence of cirrhosis), or additional use of ribavirin. Further, the sub-analyses did not produce statistically significant results (p>0.05 in all analysis). Treatment in patients receiving therapy for 24 weeks was more effective in those who received sofosbuvir with daclatasvir; however, as only two patients received sofosbuvir with simeprevir for 24 weeks, this result should again be interpreted with caution.

Patients treated with other DAA options

In total, 41 patients were treated with different DAAs from those previously described; 18 received daclatasvir with simeprevir, 12 received sofosbuvir with ribavirin, two were treated with pegylated interferon with sofosbuvir and ribavirin, eight were treated with ledipasvir with sofosbuvir, and one received pegylated interferon with daclatasvir and ribavirin. Three of these patients did not achieve SVR (one treated with daclatasvir and simeprevir, and two with sofosbuvir with ribavirin). Baseline data and results for these patients are detailed in Table 3.

Table 3.

Response rates for patients treated with other DAA options.

Treatment  n  Treatment duration (weeks)  GT  Cirrhosis (%)  Prior treatment (%)  SVR (%) 
Interferon+sofosbuvir+RBV  12 (100%)  3 (100%)  50%  0%  100% 
Ledipasvir+sofosbuvir±RBV  12 (87%) or 24 (13%)  1 (62%) and 3 (38%)  13%  75%  100% 
Sofosbuvir+RBV  12  12 (91%) or 24 (9%)  2 (100%)  66%a  17%  83% 
Daclatasvir+simeprevir±RBV  18  12 (61%) or 24 (39%)  1 (72%), and 3 (28%)  88%b  44%  94% 
Interferon+daclatasvir+RBV  24 (100%)  4 (100%)  0%  0%  100% 

Three patients missing data.


Nine patients missing data. Abbreviations: GT, genotype; RBV, ribavirin; SVR, sustained virological response.

Factors associated with SVR and tolerability events

Bivariate logistic regression was used to assess the influence of several baseline parameters on treatment response (Fig. 2). Sex, age, cirrhosis, prior treatment, treatment duration, use of ribavirin, baseline viral load, and therapy choice were not associated with treatment success (p>0.05). The only two statistically significant predictors of treatment response (both p<0.05) were genotype 1 compared with genotype 3 (OR 0.41 [CI 0.17–0.98]) and RVR response (OR 0.16 [CI 0.03–0.72]).

Fig. 2.

Predictors of sustained virological response (SVR). Abbreviations: DAC, daclatasvir; GT, genotype; RBV, ribavirin; RVR, rapid virological response. SOF, sofosbuvir; SMV, simeprevir; w, weeks.

Regarding tolerability, only three patients (1%) discontinued treatment due to adverse events, but all achieved SVR. The first was treated with pegylated interferon with sofosbuvir and ribavirin, and discontinued treatment due to epigastralgia. The second received sofosbuvir with daclatasvir, and suspended treatment due to gastric hemorrhage. The third also received sofosbuvir with daclatasvir but the reason for treatment discontinuation was not described.


The second generation DAAs evaluated in this observational study produced significant SVR rates. The results are in agreement with previous clinical trials and systematic reviews.12–14 As such, it appears that the findings obtained in controlled studies are being experienced in clinical practice in Brazil. Previous observational studies17–19 conducted in other Brazilian states have shown overall SVR rates of 93–100%, which is not very different from the findings of the present study (91.6%).

Besides the high response rates, some points must be noted. GT 3 appears to be the most difficult to treat and is the second most common genotype in Brazil (after genotype 1). However, only two treatment options are available in the country to date: sofosbuvir with daclatasvir and sofosbuvir with peginterferon alfa plus ribavirin. Previous observational studies have also shown a lower SVR rate for GT 3 patients.17,20–22 Other international guidelines, such as those of the European Association for the Study of the Liver (EASL) and the American Association for the Study of Liver Diseases (AASLD) recommend other treatment options for GT 3,7,8 such as sofosbuvir with velpatasvir, or elbasvir with grazoprevir. It is also important to mention that many of these patients received treatment of sofosbuvir with daclatasvir for a short duration (12 weeks), which may have influenced the SVR rate in these cases. Recently, the Brazilian government has approved the extension of the sofosbuvir with daclatasvir treatment to 24 weeks for cirrhotic patients.4 This, together with the addition of other drugs could increase the likelihood of cure for patients with GT 3.

GT 1, which is the most prevalent in Brazil, used to be the most difficult to treat genotype for many years.23,24 Second generation DAAs is effective for treating GT 1 infection, with SVR rates around 90%. In this study, patients with GT 1 presented higher SVR rates than those with GT 3 when treated with sofosbuvir and daclatasvir.

Few statistically significant differences were found between the factors predicting SVR. However, patients who achieved RVR had a greater likelihood of also achieving SVR. Other studies that performed similar analysis found that liver function and platelet count were factors associated with SVR.25–27

The stage of disease, i.e., fibrosis stage and presence/absence of cirrhosis, is recognized as an influence on SVR. Our analysis did not show this correlation, probably due to a considerable amount of missing data for this variable, and the difference in the number of patients in each treatment group. Nevertheless, patients with severe fibrosis should always be carefully monitored. A previous study has also suggested that liver fibrosis and HIV coinfection influences treatment outcome.28

Patients with GT 1 treated with sofosbuvir and daclatasvir had similar SVR rates than those treated with sofosbuvir and simeprevir. A pharmacoeconomic study analyzing these two treatment options, as well as other treatment options, could help health professionals to make clinical decisions regarding therapeutic choice.

Some limitations of our study should be noted. Caution should be taken when generalizing the results to other Brazilian regions and other countries, due to regional variations. Further, the absence of some information, especially fibrosis stage, may have compromised some of the analysis.


The results of this observational study confirm that second generation DAAs are effective for the treatment of chronic hepatitis C patients in Southern Brazil, particularly for genotype 1. Genotype 3 appears to be the most difficult to treat, but even so, current SVR rates with second generation DAAs were higher than with previous therapies.


This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Conflicts of interest

The authors declare no conflicts of interest.


We would like to express our thanks to the Brazilian Hepatology Society (Sociedade Brasileira de Hepatologia; SBH) for sharing the data collection table and for all research support.

Appendix A
Supplementary data

The following are the supplementary data to this article:

World Health Organization (WHO). Hepatitis C Fact Sheet No 164 (Updated July 2017). Available from: [accessed 10.08.17].
D. Lavanchy
The global burden of hepatitis C
D. Lavanchy
Evolving epidemiology of hepatitis C virus
Clin Microbiol Infect, 17 (2011), pp. 107-115
Brasil,Ministério da Saúde,Secretaria de Vigilância em Saúde,Departamento de DST, Aids e Hepatites Virais
Protocolo Diretrizes Clínico e Terapêuticas para Hepatite C e Coinfecções
Ministério da Saúde, (2017)
European Association for the Study of the Liver (EASL)
EASL Clinical Practice Guidelines: management of hepatitis C virus infection
J Hepatol, 55 (2011), pp. 245-264
M.S. Sulkowski,C. Cooper,B. Hunyady
Management of adverse effects of Peg-IFN and ribavirin therapy for hepatitis C
Nat Rev Gastroenterol Hepatol, 8 (2011), pp. 212-223
European Association for the Study of the Liver (EASL)
EASL recommendations on treatment of hepatitis C 2015
J Hepatol, 63 (2015), pp. 199-236
American Association for the Study of Liver Diseases/Infectious Diseases Society of America (AASLD-IDSA)
Recommendations for testing, managing, and treating hepatitis C
World Health Organization (WHO)
Guidelines for the screening, care and treatment of persons with hepatitis C infection
World Health Organization, (2014)
F. McPhee,D. Hernandez,N. Zhou
Pooled analysis of HCV genotype 1 resistance-associated substitutions in NS5A, NS3 and NS5B pre- and post-treatment with 12 weeks of daclatasvir, asunaprevir and beclabuvir
Antivir Ther, 23 (2018), pp. 53-66
V. Soriano,P. Labarga,J.V. Fernandez-Montero
Hepatitis C cure with antiviral therapy-benefits beyond the liver
Antivir Ther, 21 (2016), pp. 1-8
V.L. Ferreira,F.S. Tonin,N.A. Assis Jarek,Y. Ramires,R. Pontarolo
Efficacy of interferon-free therapies for chronic hepatitis C: a systematic review of all randomized clinical trials
Clin Drug Investig, 37 (2017), pp. 635-646
V.L. Ferreira,N.A. Assis Jarek,F.S. Tonin
Ledipasvir/sofosbuvir with or without ribavirin for the treatment of chronic hepatitis C genotype 1: a pairwise meta-analysis
J Gastroenterol Hepatol, 32 (2017), pp. 749-755
V.L. Ferreira,N.A. Assis Jarek,F.S. Tonin,H.H. Borba,A. Wiens,R. Pontarolo
Safety of interferon-free therapies for chronic hepatitis C: a network meta-analysis
J Clin Pharm Ther, 41 (2016), pp. 478-485
A.W. Mariani,P.M. Pego-Fernandes
Observational studies: why are they so important?
Sao Paulo Med J, 132 (2014), pp. 1-2
R.J. Ligthelm,V. Borzì,J. Gumprecht,R. Kawamori,Y. Wenying,P. Valensi
Importance of observational studies in clinical practice
Clin Ther, 29 (2007), pp. 1284-1292
H. Cheinquer,H. Sette Jr.,F.H. Wolff
Treatment of chronic HCV infection with the new direct acting antivirals (DAA): First report of a real world experience in Southern Brazil
Ann Hepatol, 16 (2017), pp. 727-733
T. Medeiros,C.M. Salviato,N.F. do Rosario
Adverse effects of direct acting antiviral-based regimens in chronic hepatitis C patients: a Brazilian experience
Int J Clin Pharm, 39 (2017), pp. 1304-1311
N. Miotto,L.C. Mendes,L.P. Zanaga
Predictors of early discontinuation of interferon-free direct antiviral agents in patients with hepatitis C virus and advanced liver fibrosis: results of a real-life cohort
Eur J Gastroenterol Hepatol, 29 (2017), pp. 1149-1154
G.R. Foster,W.L. Irving,M.C. Cheung
Impact of direct acting antiviral therapy in patients with chronic hepatitis C and decompensated cirrhosis
J Hepatol, 64 (2016), pp. 1224-1231
J. Young,N. Weis,H. Hofer
The effectiveness of daclatasvir based therapy in European patients with chronic hepatitis C and advanced liver disease
BMC Infect Dis, 17 (2017), pp. 45
V.L. Ferreira,L.P. Leonart,F.S. Tonin,H.H.L. Borba,R. Pontarolo
Sustained virological response in special populations with chronic hepatitis C using interferon-free treatments: a systematic review and meta-analysis of observational cohort studies
Clin Drug Investig, (2018),
[Epub ahead of print]
C. Camma,S. Petta,M. Enea
Cost-effectiveness of boceprevir or telaprevir for untreated patients with genotype 1 chronic hepatitis C
Hepatology, 56 (2012), pp. 850-860
I. Shahid,W.H. Almalki,M.H. Hafeez,S. Hassan
Hepatitis C virus infection treatment: an era of game changer direct acting antivirals and novel treatment strategies
Crit Rev Microbiol, 42 (2016), pp. 535-547
H.R. El-Khayat,Y.M. Fouad,M. Maher,H. El-Amin,H. Muhammed
Efficacy and safety of sofosbuvir plus simeprevir therapy in Egyptian patients with chronic hepatitis C: a real-world experience
M. Kobayashi,F. Suzuki,S. Fujiyama
Sustained virologic response by direct antiviral agents reduces the incidence of hepatocellular carcinoma in patients with HCV infection
J Med Virol, 89 (2017), pp. 476-483
J.L. Calleja,J. Crespo,D. Rincon
Effectiveness, safety and clinical outcomes of direct-acting antiviral therapy in HCV genotype 1 infection: results from a Spanish real-world cohort
J Hepatol, 66 (2017), pp. 1138-1148
A. Arias,A. Aguilera,V. Soriano
Rate and predictors of treatment failure to all-oral HCV regimens outside clinical trials
Antivir Ther, 22 (2017), pp. 307-312
Copyright © 2018. Sociedade Brasileira de Infectologia
The Brazilian Journal of Infectious Diseases

Subscribe to our Newsletter

Article options
Supplemental materials
Cookies policy
To improve our services and products, we use cookies (own or third parties authorized) to show advertising related to client preferences through the analyses of navigation customer behavior. Continuing navigation will be considered as acceptance of this use. You can change the settings or obtain more information by clicking here.

Are you a health professional able to prescribe or dispense drugs?