Skip to main content

Impact of new DAA therapy on real clinical practice: a multicenter region-wide cohort study



Management of chronic hepatitis C (CHC) has significantly accelerated in the last few years. Currently, second generation direct acting antivirals (DAAs) promise clearance of infection in most of patients. Here we present the results of the first analysis carried out on data of Lazio clinical network for DAAs.


The study was designed as a multicenter cohort: a) to assess the evolution of treatment during the first 24 months of the activity of the Clinical Network; b) to report overall efficacy of treatments; c) to analyze potential factors associated with lack of virological response at 12 weeks after therapy (SVR12); d) to evaluate the variation of ALT at baseline and 12 weeks after therapy in those who achieved SVR12 in comparison to those who did not. Analyses of efficacy were carried out with multilevel mixed effect logistic regression model. ALT temporal variation was assessed by mixed effect model mixed models with random intercept at patient’s level and random slope at the level of the time; i.e. either before or after therapy.


Between 30 December 2014 and 31 December 2016 5279 patients started a DAA treatment; of those, 5127 (in 14 clinical centers) had completed the 12-week follow-up. Overall proportion of SVR12 was 93.41% (N = 4780) with no heterogeneity between the 14 clinical centers. Interruption as the consequence of severe side effect was very low (only 23 patients). Unadjusted analysis indicates that proportion of SVR12 significantly changes according to patient’s baseline characteristics, however after adjusting for potential confounders only adherence to current guidelines, stage of liver diseases, gender, transplant and HIV status were independently associated with the response to therapy. Analysis of ALT temporal variation showed that ALT level normalized in most, but not, all patients who achieved SVR12.


Our study confirmed the extraordinary efficacy of DAAs outside clinical trials. The advantage of DAAs was particularly significant for those patients who were previously considered as difficult-to-treat and did not have treatment options before DAAs era. Intervention based on network of select centers and prioritization of patients according to diseases severity was successful. Further studies are needed to establish whether clearance of HCV after DAAs therapy can arrest or even revert liver fibrosis in non-cirrhotic patients and/or improve life quality and expectancy in those who achieve SVR12 with cirrhosis.

Peer Review reports


The hepatitis C virus (HCV) has been firstly identified in 1989 as a blood-borne human pathogen [1, 2]. Acute infection with HCV is often asymptomatic, however about 80% of infected people cannot clear the virus and develop chronic infection [3, 4]. It is estimated that chronic hepatitis C (CHC) kills about 700,000 people each year at global level [5].

Clinical approach for CHC has gradually improved over the last 30 years [6]. However, since 2014 management of CHC has been re-invented by the introduction of the direct acting antivirals (DAAs) [7]. Registered clinical trials showed that the combinations of second generation DAAs can achieve HCV clearance in most of HCV infected subjects including difficult-to-treat patients (e.g. those with cirrhosis, transplant recipients, therapy experienced patients and HIV co-infected subjects) [8]. These astonishing results have been confirmed by clinical observational studies [9,10,11,12] suggesting that currently anti-HCV therapy may be see also as a public health intervention aimed to control, and potentially, eliminate HCV [1, 7, 13, 14].

For maximizing the impact of new therapy at population level, many National Health Systems promoting universal access to care [15], have implemented DAAs into clinical practices using different strategies tailored on the local epidemiology of CHC and on the availability of economic resources. Two main strategies [16] have been proposed: a) treatment as prevention, targeted to reduce incidence of new HCV infections; b) prioritization for the stage of the disease, targeted to minimize CHC associated morbidity and mortality.

According to the Italian National Policies, since January 2015 the health authority of Lazio (an administrative Region in central Italy) has implemented a strategy for the access to DAAs based the on prioritization of patients with advanced liver diseases, extrahepatic manifestation and others severe clinical manifestations.

Here we present the results of the first analysis carried out on data of Lazio clinical network for DAA.


Study design and aims

This is a multicenter prospective cohort study enrolling patients with CHC who receive therapy with second generation DAAs in Lazio. Here we report the analyses carried out: A) to describe access to DAAs in the Region and to assess the resilience of the network to changing policies and guidelines; B) to assess association between treatment outcome and patient’s epidemiological and clinical characteristics; C) to evaluate temporal variation of ALT level before therapy and 12 weeks after the end of treatment.


Lazio is an Italian Region with about 5.6 million inhabitants. About 47% of Lazio inhabitants live in Rome, the only large city. All other people live in the 347 municipalities, mainly towns (median habitants 2674 IQR 1120–7997). The Italian National Health System endorsed scheme for reimbursement of DAAs therapies based on stage of liver disease. These schemes guaranteed free access to DAAs to all subjects with CHC according to 7 criteria (five additional criteria to expand access to DAAs have been recently established) [17].

Until the end of 2016 these criteria prioritized for treatment with DAAs patients with cirrhosis (CHILD A and B) and/or resected HCC, patients with advanced liver fibrosis (Metavir F3), transplant recipients, candidates to liver transplant, patients with severe extrahepatic manifestations and patients with METAVIR F2 liver fibrosis with co-morbidities (HIV/HBV co-infections, non-viral hepatitis, diabetes, BMI ≥30, hemoglobinopathies and coagulation disorders). To implement the national reimbursement scheme and to guarantee equal access to care, Lazio Regional Health Authority has centralized DAAs supplies and created a clinical network consisting of 14 selected clinical centers for evaluation and treatment of patients with CHC. In Lazio, no patient outside this clinical network could receive DAA therapy under the national reimbursement scheme.

Participants and follow-up

Patients were eligible for analysis if they received therapy for CHC in the Lazio and:

  1. A.

    received for the first time one or more of the subsequent drugs: sofosbuvir (SOF), simeprevir (SIM), daclatasvir (DAC), ledipasvir (LED), ombitasvir+paritaprevir+ritonavir± dasabuvir (2D/3D);

  2. B.

    started therapy between 30 December 2014 and 31 December 2016

For each patient, we analyzed the following information at:

  1. A.

    Start of therapy: code of the clinical center; date of start of therapy; criterion for access to DAA, DAA regimen; age; gender; HCV RNA; HCV genotype; body max index (BMI); stage of liver diseases, HBsAg; anti-HIV Ab; status for previous therapy; ALT; history of OLT and of HCC;

  2. B.

    end of therapy: date of end of therapy; life status; whether therapy was interrupted as consequence of severe adverse reaction;

  3. C.

    12 weeks after the end of therapy: date of data collection; HCV RNA; life status; ALT.

Treatment outcome

Treatment was successful if patient was alive and with undetectable HCV RNA level at 12 weeks after the end of therapy (sustained virological response at 12 weeks after therapy; SVR12).

Treatment failed if at 12 weeks after the end of therapy patient either: A) had detectable HCV RNA level; B) started a new anti-HCV treatment; C) has died.

Data sources and measurement

All data analyzed come from the Lazio Regional Network for DAAs. The network has been operational since 30 December 2014 and it was formally enforced by a Regional Act on 12 February 2015. Patient’s clinical characteristics at enrollment were analyzed as reported by doctors who evaluated patients for eligibility to national reimbursements scheme. Detection of HCV RNA in blood was performed by sensitive quantitative molecular assays with lower limit of detection as declared by manufacturer (in all cases ≤15 international units/ml); HCV genotype was determined by method able to distinguish between genotype 1a and genotype 1b. ALT level was quantified with standard laboratory methods implemented in local clinical centers.

For the purpose of this study we used the 2016 EASL guidelines [8] for defining 3 groups of quality of treatments: group A, treatments considered as optimal in 2016 EASL guidelines; group B, treatments that were shorter than recommended and/or did not include all the recommended drugs/combinations and thus were considered suboptimal in 2016 EASL guidelines; group C, treatments that contained all drugs as group A, but also included additional drug (e.g. ribavirin; RBV) and/or it were longer than recommended. This rating was meant for assessing the resilience of the network in the rapidly changing scenario and not for evaluating the performance of the individual clinical centers.


Association between patients’ clinical characteristics and treatment outcome (SVR12) was analyzed in bivariable and multivariable mixed effect multilevel logistic (MEML) regression models with random intercept to correct for the effect of correlation of data at level of the clinical centers. Bivariable models were used to estimate proportions of SVR12, to assess potential heterogeneity across clinical centers and to estimates unadjusted association between proportion of SVR12 and patient’s clinical features. Multivariable MEML was implemented to adjust for the effect of potential confounders using all covariates with p < 0.100 in the bivariable analysis. Odds-ratio (OR) for failing (i.e. the complement of SVR12) was used to describe the association between the risk of treatment failure and patient’s characteristics.

Changes of ALT at baseline and 12 after the end of therapy was assessed for the four groups of patients (i.e. non-cirrhotic patients with SVR12; non-cirrhotic patients without SVR12; cirrhotic patients with SVR12 and non-cirrhotic patients without SVR12). The estimates were calculated by a balanced (i.e. all patients had value of ALT at before and 12 weeks after therapy) linear mixed effect model with random intercept at the level of patients and random slope at the level of time. We have previously validated these model in the analysis of complex clinical datasets [18, 19]. Overall the model included ALT level as the unique continuous dependent variable and 3 independent binary variables i.e.: time (either at before therapy or 12 weeks after therapy); clinical outcome (either SVR12 or failure) and presence of cirrhosis before therapy (either yes or no) allowing for full interaction between them.

All analyses and plots were implemented by STATA 13.1 statistical package.


Figure 1 shows the subsets of population included in the different analyses.

Fig. 1
figure 1

Flow charts to describe selection of population sample included in the different analyses. Blue boxes report the number of patients in each stage of selection; green boxes report excluded subjects with reason; orange boxes report the type of analysis carried out

Access to therapy with new DAA

Between 30 December 2014 and 31 December 2016 5279 patients initiated 5350 DAA treatments in Lazio. Seventy-one treatments were given as given as second line-treatment and were excluded from the analysis. Overall the analysis included all the 5279 patients at the time of their first treatment with DAAs.

Figure 2 shows the number of patients by the time when therapy was started and DAA combination used. Among the 5279 patients who received first line treatment with DAAs, SOF was the most used drug (87.07%; N = 4438) followed by LED (36.92%; N = 1949) DAC (20.06%; N = 1059), 2D/3D combinations (14.76%; N = 779) and SIM (13.71%; N = 724). RBV was used in about half of all DAA scheme (49.69%; N = 2623) while the use of pegylated interferon in combination either with SOF (1.48%; N = 78) or SIM (1.18%; N = 62) plus RBV was marginal and limited to the earliest period only Treatment intended duration ranged between 8 and 48 weeks, but almost all the treatments were planned for a duration of either 12 (57.81%; N = 3052) or 24 weeks (41.37%; N = 2184). Only few DAA treatments were planned for a duration of either 8 (0.45% N = 24), 16 (0.08% N = 4) or 48 weeks (0.28% N = 15) (Table 1).

Fig. 2
figure 2

Distribution of the 5279 DAA naïve patients according to DAAs combination and month of start of therapy. SOF: sofosbuvir±ribavirin±Peg-Interferon; SIM: simeprevir+ribavirin+Peg-interferon. 2D/3D: ombitasvir+paritaprevir+ritonavir±dasabuvir±ribavirin; LED+SOF: ledipasvir+sofobuvir; DAC + SOF: daclatasvir+sofosbuvir. The frequency of each specific combination is reported in Table 1

Table 1 DAA treatments schemes

The proportion of patients who received DAA combinations consistent with EASL 2016 guidelines was very low until May 2015 and eventually steadily increased between June 2015 and December 2016 when the 73.68% of all treatment were consistent with EASL 2016 guidelines (Fig. 3a). however, the analysis of DAA combination according to previous guidelines suggested that: A) for treatments started under EASL 2014 GL (i.e. by 21st April 2015) none could be classified as sub-optimal; B) for treatments started under EASL 2015 GL (i.e. after 22nd April 2016) 269 can be classified as sub optimal, the main reason was under use of ribavirin in cirrhotic patients in genotype 1 and 3 (N = 221; 82%); C) for treatments started under EASL 2016 GL (i.e. after 22nd September 2016) 89 can be classified as sub optimal, the main reason was under use of ribavirin in cirrhotic patients with genotype 3 (N = 30; 44%) and use of SOF + RBV in gen 2 (N = 28; 32%).

Fig. 3
figure 3

Proportion of the patients according quality of treatment and urgency of treatment. a Monthly proportion of the 5279 patients who received either sub-optimal, optimal or not recommend of treatment according to EASL 2016 guidelines. Group A, treatments currently considered as optimal in 2016 EASL guidelines; group B, treatments that is shorter than currently recommended and/or does not included all the recommended drugs/combinations and thus considered suboptimal in 2016 EASL guidelines; group C, treatments that contains all drugs as group A, but also included additional drug (e.g. ribavirin RBV) and/or it is longer than currently recommended. NA: not assessable (patients’ information to assess quality are missing). b Monthly proportion of the 5279 patients who had access to therapy by base line clinical features. Urgent:: patients with cirrhosis, candidate to liver transplant; recipients of organ transplant, patients with severe HCV associated extra-hepatic manifestation; Non cirrhotic: all other patients

The proportion of patients who received DAA without cirrhosis steadily increased over time being none during the first 2 months of the study period and 51.05% by December 2016 (Fig. 3b).

Treatment efficacy at 12 weeks after the end of therapy

The overall proportion of lost to follow-up was 2.88% (152 out of 5279 patients who started therapy). The bivariable analysis of efficacy was carried out on the 5127 patients who had completed the follow-up at 12 weeks post treatment. Overall SVR12 proportion was 93.41% (95% CI 92.48–94.34%) with no evidence of heterogeneity across clinical centers (p for heterogeneity in null model = 0.219).

In total 347 (6.59%) patients did not achieve SVR12; among them, 72 patients died by week 12 post-treatment (31 of whom during treatment) and only 23 patients interrupted the treatment for drug toxicity.

Table 2 shows descriptive analysis and the results of bivariable MEML models to assess potential association between SVR12 and individual patient’s characteristics. Proportions of SVR12 significantly change according to all analyzed patients’ baselines characteristics apart from age and previous history of treatment (range: 76.60–96.48%; see Table 2). Table 3 shows the results of multivariable MEML model to adjust for potential confounding bias. This model showed that after adjusting for other co-variates the treatment group (p < 0.001), stage of liver diseases (p < 0.001), gender (p < 0.001), OLT (p = 0.005) and HIV serostatus (p = 0.019) where significantly associated with SVR12. In addition, no heterogeneity for efficacy across clinical centers was observed (p for heterogeneity in multivariable MEML = 1.000).

Table 2 Descriptive analysis and the results of bivariable MEML models for efficacy
Table 3 Multivariable MEML model for efficacy

Temporal variation of ALT level before therapy and at 12 weeks after the end of treatment

Figure 4 shows the temporal variation of ALT level before therapy and 12 weeks after the end of treatment in the four different classes of patients; i.e.: patients with cirrhosis who did not achieve SVR12; patients with cirrhosis who achieved SVR12; patients without cirrhosis who did not achieve SVR12; patients without cirrhosis who achieved SVR12. This analysis was carried out on a convenient sample of 3179 subjects who had ALT determination both before start of therapy and at the end of the follow-up.

Fig. 4
figure 4

Kinetics of ALT level in 4 different groups of patients according to the stage of liver disease (i.e. with/without cirrhosis) and therapy outcome (i.e. fail or SVR12). a Box-plot describe the distribution of the 3179 patients according values of ALT level patients either before the start of therapy (blue boxes; T0) and eventually 12 weeks after therapy (red boxes; FUP12). Almost all patients had ALT value above upper normal limit (black dotted line; 40 U/L) before therapy. More than 75% of patients who achieve SVR12 normalized ALT at 12 weeks after the end of therapy. A normalization of ALT values was also reported in about 50% of those who did not achieve SVR at 12 weeks after the end of therapy. b Temporal variation of ALT levels before treatment and 12 weeks after the endo of therapy. Estimates, 95%CI and p-values were carried out according to a mixed effect model which take in account correlation of data at the level of each individual patients. A significant reduction of ALT is reported for all patients. However average reduction of ALT levels is about 2 time higher in those who achieved SVR12 than in those who did not

Figure 4a shows the distribution of ALT levels for the 3179 patients included in the analysis (overall 6358 ALT determinations). ALT levels were above the upper normal limit (40 U/L) in more than 75% of patients before treatment (blue boxes in Fig. 4a). In contrast, at 12 weeks after therapy, ALT levels normalized in more than 75% of patients with SVR12 and in about 50% of those who failed, regardless the stage of liver diseases, (red boxes in Fig. 4a).

Average reduction of ALT levels before therapy and 12 weeks after therapy, 95% CI and p-value according to stage of liver diseases (i.e. either with or without cirrhosis) and outcome of therapy (i.e.: either SVR12 or fail) are reported in Fig. 4b. This analysis provides strong evidence that ALT significantly decreased in all patients. However, the degree of reduction was more than 2 times higher in those who achieved SVR12 than in those who did not.


To our knowledge, this is one of the largest prospective observational study carried out using real clinical data of patients treated with second generation DAAs. Real world studies like this are pivotal to assess the actual impact of new therapies on real clinical practice and to confirm efficacy and safety of new drugs outside clinical trials.

We showed that Lazio clinical network was capable of timely dealing with the changing guidelines and the ongoing process of approval drug. Newly DAAs were included in treatment with no delay, besides, the adherence to current standard of care steadily increased over time following to the publication of new guidelines. In addition, the number of patients who started therapy with cirrhosis steadily decreased over time, suggesting that the patients with advanced liver disease and replicating HCV infection have been steadily decreasing. For these reasons, since April 2017 the Italian policies for reimbursement of DAAs have been extended to include several sub-groups of patients in addition to those with urgent need of therapy [17].

We found that overall efficacy of DAAs therapies was well above 90% (i.e.: 93.41% with a 95% CI between 92.48 and 94.34%) which is within the efficacy range reported in clinical trials [20]. A large real world clinical study carried out in USA enrolling 4365 patients with HCV genotype 1 infection reported slightly lower efficacy rate with SVR12 between 91.3 and 92.0% [21]. This marginal difference could be due to differences in baseline characteristics; the USA study includes only genotype 1 and about 36.5% of African-American patients, in whom SVR12 rates were significantly lower than in European ones (89.8% vs. 92.8%). In addition, better proportion of SVR12 in our study compared to the USA cohort may be due to different patient management, as acknowledged by Calleja et al. [22] Indeed, multicenter prospective cohort studies carried out in other European settings, such as Spain [23] and Germany [24, 25], reported proportions of SVR similar to those observed in our study. In our clinical network, patients were managed by experienced clinicians in selected clinical centers rather than in community-based practice, which may have resulted in better adherence to treatment and consequently higher SVR12 rate [26]. The circumstance that our patients received homogeneously high quality of care throughout the Region was confirmed by no heterogeneity of efficacy across clinical centers and the very low level of lost to follow-up.(2.88%) Indeed, lost to follow-up proportion was more than 2 times lower than that reported in USA (6.80%) and comparable to those observed in similar clinical setting in Spain (2.71%) [23] and Germany (4.89%) [24].

After adjusting for other confounders, we found that quality of treatment, stage of liver diseases, gender, OLT and HIV serostatus were independent predictors of SVR12.

Our study includes a considerable number of patients who received a quality of treatment currently considered as either sub-optimal (group B) or not recommended (group C) [8]. This mirrors the dynamic real-world scenario analyzed, where standard of care changed according to the availability of additional DAAs and new clinical recommendations. In Italy SOF became reimbursable from December 2014, SIM from February 2015, DAC from April 2015 and SOF + LDV, 2D and 3D from May 2015. When the clinical network was established, effective EASL guidelines were those available since May 2014 [27] which were updated on April 2015 [28] and eventually on September 2016 [8]. As in other prospective studies carried out in Italy [10], our study provided strong evidence that adherence to the most current standards of care was associated with higher proportions of SVR12 than receiving DAAs combinations which were eventually considered sub-optimal. In addition, we did not find significant association between failure and not recommended, though not suboptimal, treatments, as those included in group C.

Cirrhosis remains a significant challenge in the DAAs era. Although, the observed efficacy of DAA therapies was much higher than that expected for interferon plus ribavirin therapies [6], unadjusted analysis showed that SVR12 dropped from 95.99% in patients without cirrhosis to 76.70% in those with decompensated cirrhosis. Multivariable analysis confirmed this observation and provided evidence that, in comparison with patients without cirrhosis, the risk of failing SVR12 was 1.56 and 5.39 times higher in patients with either compensate or decompensate cirrhosis, respectively. Unadjusted proportions of SVR12 in patients with cirrhosis were slightly lower in our population than those estimated in other studies where patients with cirrhosis received SOF in combination with either DAC [29,30,31] or LED [30,31,32]. The difference may be due to the unavailability of such regimens in the earliest period of the study, when SOF in combination with RBV was the only available combination.

We found that females exhibited higher proportion of SVR12 than males. The role of gender as predictor of response to anti-HCV therapies has been debated since long before DAAs introduction. Population studies provided evidence that females were more likely than males to naturally clear HCV after infection [33]. Clinical studies suggested that young females had better response to interferon therapy than males [34,35,36] but menopause may abolish this advantage [37]. Recent clinical experiences with DAAs seem to confirm this observation [24, 38], however whether a causal (biological) link stands behind the association between gender and response to anti HCV therapies is unclear, yet. The explanation of the potential biological pathways of the association between SVR12 and gender is beyond the scope of this study. Nevertheless, it is worth of notice that our estimate (OR 1.84 95% CI 1.40–2.43) is widely consistent with those reported in similar large prospective studies carried out in Europe [23, 24, 39, 40].

We found that HIV serostatus was an independent predictor of SVR12. The potential effect of HIV serostatus on efficacy of new DAAs therapies is currently debated. Bischoff et al. [39] found that HIV positive and HIV negative subjects had similar proportion of SVR12 (90.3 and 91.2%, respectively). However, these results may be the consequence of confounding as prevalence of cirrhosis was significantly higher among HIV negative than among HIV positive subjects (29.5% vs 17.2%, respectively; p < 0.001) and authors did not adjust statistics for the level of liver diseases in the multivariable analysis. In contrast, Neukam et al. [41], reported that, after adjustment for potential confounders, including cirrhosis, HIV positivity was associated with lower proportion of SVR12. Moreover, recent studies specifically focused on HIV positive population reported proportions of SVR consistent to those observed in our study and emphasize that level of CD4 is directly associated with SVR12 [40]. Consistently with these latter experiences our study suggests that, even if DAAs are very effective in HIV positive subjects (with SVR12 portion higher than 90%), patient with HIV may still have marginally lower proportion of SVR12 than those without HIV infection.

We found a proportion of SVR among OLT recipients of 87.75% (95 82.11–93.39%) which is significantly lower than SVR in subjects without OLT. This is one of the first large prospective study which attempted to assess association between OLT and SVR. Our observation is consistent with punctual estimates of SVR proportion reported in prospective studies enrolling OLT patients only [42, 43].

Finally, our study provided strong evidence that DAAs therapy was associated with a significant reduction of liver cytolysis. The role of DAAs in the reduction of liver damage has been already suggested by a previous study [44]. However, we found that ALT levels normalized in most, but not all, patients who achieved SVR12, implying that hepatic inflammation may continue in a sub set of patients despite HCV clearance [45]. This finding also suggest that patients who achieved SVR12 would need long-term clinical follow-up to monitor the improvement of liver diseases and further underlines that HCV infection may be associated with comorbidities that on one hand contribute to the progression of the disease and, on the other hand, need to be managed once HCV has been eradicated.

Limitation of our study are related to: A) observational design, thus confounding due to unmeasured exposures cannot be ruled out; B) even though the information were collected through a compulsory system enforced by Regional laws, we still had a moderate proportion of missing data; C) analysis to assess the effect of SVR on hepatic cytolysis was carried out on convenient sub set of patient for whom ALT determinations were available; D) we do not systematically collect data on resistance before therapy, this limitation may be marginal for the purposes of our analyses as current guidelines does not recommend resistance testing prior to treatment with DAAs and acknowledge that treatment regimens can be optimized without this information [8].


In conclusion, our study confirmed the extraordinary efficacy of DAA therapies outside clinical trials and provided evidence that adherence to most current guidelines can further improve the response rate in all patients. The advantage of using DAAs was particularly significant for those patients who were previously considered as difficult-to-treat and had no-treatment option before DAAs era. As in other European experiences, our model of intervention based on the creation of a network of select clinical centers and prioritization of patients according to diseases severity was successful and guaranteed timely implementation of new drug combinations, high level of SVR12 and the significant reduction of patients with advance stage CHC in urgent need of therapy. Our study analyzed as the only outcome clearance of HCV infection (i.e. SVR12) thus it provides no information about the actual impact of DAAs therapy on patient’s life quality and expectancy after SVR. Further studies are needed to establish whether clearance of HCV after DAAs therapy can arrest, or even revert, liver fibrosis in non-cirrhotic patients and/or improve life expectancy in those who achieved SVR12 with advanced stage live disease [46]. In our opinion, long term clinical follow-up is needed also in patients who achieved SVR12.







Alanine aminostransferase


Body max index


Chronic hepatitis C


Direct acting antivirals




European Association for the study of the liver


Hepatocellular carcinoma


Hepatitis C virus


Human immunodeficiency virus




Mixed effect multilevel logistic


Orthotopic liver transplant




Ribonucleic acid






Sustained virological response at 12 weeks after therapy


  1. Choo QL, Kuo G, Weiner AJ, Overby LR, Bradley DW, Houghton M. Isolation of a cDNA clone derived from a blood-borne non-a, non-B viral hepatitis genome. Science. 1989;244(4902):359–62. PubMed PMID: 2523562.

    Article  PubMed  CAS  Google Scholar 

  2. Lanini S, Easterbrook PJ, Zumla A, Ippolito G. Hepatitis C: global epidemiology and strategies for control. Clin Microbiol Infect. 2016;22(10):833–8. Epub 2016 Aug 11. Review. PubMed PMID: 27521803.

    Article  PubMed  CAS  Google Scholar 

  3. Koretz RL, Lin KW, Ioannidis JP, Lenzer J. Is widespread screening for hepatitis C justified? BMJ. 2015;350:g7809. PubMed PMID: 25587052.

    Article  PubMed  Google Scholar 

  4. Ahmad J, Hepatitis C. BMJ. 2017;358:j2861. PubMed PMID: 28684552.

    Article  PubMed  Google Scholar 

  5. WHO. Hepatitis C Fact sheet N°164. Accessed 05 May 2018.

  6. Heim MH. 25 years of interferon-based treatment of chronic hepatitis C: an epoch coming to an end. Nat Rev Immunol. 2013;13(7):535–42. Epub 2013 Jun 7. Review. PubMed PMID: 23743475.

    Article  PubMed  CAS  Google Scholar 

  7. Ippolito G, Capobianchi MR, Lanini S, Antonelli G. Is hepatitis C virus eradication around the corner only 25 years after its discovery? Int J Antimicrob Agents. 2015;45(2):111–2. Epub 2014 Sep 6. PubMed PMID: 25249016.

    Article  PubMed  CAS  Google Scholar 

  8. European Association for the Study of the Liver. Electronic address: easloffice@easloffice.Eu. EASL recommendations on treatment of hepatitis C 2016. J Hepatol. 2017;66(1):153–94. Epub 2016 Sep 22. PubMed PMID: 27667367.

    Article  Google Scholar 

  9. Fernández Carrillo C, Lens S, Llop E, Pascasio JM, Crespo J, Arenas J, Fernández I, Baliellas C, Carrión JA, de la Mata M, Buti M, Castells L, Albillos A, Romero M, Turnes J, Pons C, Moreno-Planas JM, Moreno-Palomares JJ, Fernández-Rodriguez C, García-Samaniego J, Prieto M, Fernández Bermejo M, Salmerón J, Badia E, Salcedo M, Herrero JI, Granados R, Blé M, Mariño Z, Calleja JL. Treatment of hepatitis C virus infection in patients with cirrhosis and predictive value of model for end-stage liver disease: analysis of data from the Hepa-C registry. Hepatology. 2017;65(6):1810–22. Epub 2017 Apr 28. PubMed PMID: 28170112.

    Article  PubMed  CAS  Google Scholar 

  10. d'Arminio Monforte A, Cozzi-Lepri A, Ceccherini-Silberstein F, De Luca A, Lo Caputo S, Castagna A, Mussini C, Cingolani A, Tavelli A, Shanyinde M, Gori A, Girardi E, Andreoni M, Antinori A, Puoti M, Icona Foundation and HepaIcona Study Group. Access and response to direct antiviral agents (DAA) in HIV-HCV co-infected patients in Italy: data from the Icona cohort. PLoS One. 2017;12(5):e0177402. eCollection 2017. PubMed PMID: 28520749; PubMed Central PMCID: PMC5435319.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  11. Saxena V, Khungar V, Verna EC, Levitsky J, Brown RS, Hassan MA, Sulkowski MS, O'Leary JG, Koraishy F, Galati JS, Kuo AA, Vainorius M, Akushevich L, Nelson DR, Fried MW, Terrault N, Reddy KR. Safety and efficacy of current DAA regimens in kidney and liver transplant recipients with hepatitis C: results from the HCV-TARGET study. Hepatology. 2017; [Epub ahead of print] PubMed PMID: 28504842.

  12. Beste LA, Green PK, Berry K, Kogut MJ, Allison SK, Ioannou GN. Effectiveness of hepatitis C antiviral treatment in a USA cohort of veteran patients with hepatocellular carcinoma. J Hepatol. 2017;67(1):32–9. Epub 2017 Mar 4. PubMed PMID: 28267622.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Martin NK, Vickerman P, Grebely J, Hellard M, Hutchinson SJ, Lima VD, Foster GR, Dillon JF, Goldberg DJ, Dore GJ, Hickman M. Hepatitis C virus treatment for prevention among people who inject drugs: modeling treatment scale-up in the age of direct-acting antivirals. Hepatology. 2013;58(5):1598–609. Epub 2013 Aug 26. PubMed PMID: 23553643.

    Article  PubMed  CAS  Google Scholar 

  14. WHO Global Health Sector Strategy On Viral Hepatitis 2016–2021 Towards Ending Viral Hepatitis available at Accessed 05 May 2018.

  15. GBD 2015 Healthcare Access and Quality Collaborators. Healthcare access and quality index based on mortality from causes amenable to personal health care in 195 countries and territories, 1990-2015: a novel analysis from the global burden of disease study 2015. Lancet. 2017; [Epub ahead of print] PubMed PMID: 28528753.

  16. Innes H, Goldberg D, Dillon J, Hutchinson SJ. Strategies for the treatment of hepatitis C in an era of interferon-free therapies: what public health outcomes do we value most? Gut. 2015;64(11):1800–9. 2014 Nov 6. PubMed PMID: 25378522

    Article  PubMed  CAS  Google Scholar 

  17. AIFA Guidelines. Available from: Accessed 05 May 2018.

  18. Lanini S, Portella G, Vairo F, Kobinger GP, Pesenti A, Langer M, Kabia S, Brogiato G, Amone J, Castilletti C, Miccio R, Zumla A, Capobianchi MR, Di Caro A, Strada G, Ippolito G, INMI-EMERGENCY EBOV Sierra Leone Study Group. Blood kinetics of Ebola virus in survivors and nonsurvivors. J Clin Invest. 2015;125(12):4692–8. Epub 2015 Nov 9. PubMed PMID: 26551684; PubMed Central PMCID: PMC4665798.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Lanini S, Portella G, Vairo F, Kobinger GP, Pesenti A, Langer M, Kabia S, Brogiato G, Amone J, Castilletti C, Miccio R, Capobianchi MR, Strada G, Zumla A, Di Caro A, Ippolito G, INMI-EMERGENCY EBOV Sierra Leone Study Group. Relationship between viremia and specific organ damage in Ebola patients: a cohort study. Clin Infect Dis. 2018;66(1):36–44. PubMed PMID: 29020340.

    Article  PubMed  Google Scholar 

  20. Falade-Nwulia O, Suarez-Cuervo C, Nelson DR, Fried MW, Segal JB, Sulkowski MS. Oral direct-acting agent therapy for hepatitis C virus infection: a systematic review. Ann Intern Med. 2017;166(9):637–48. Epub 2017 Mar 21. Review. PubMed PMID: 28319996; PubMed Central PMCID: PMC5486987.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Backus LI, Belperio PS, Shahoumian TA, Loomis TP, Mole LA. Real-world effectiveness of ledipasvir/sofosbuvir in 4,365 treatment-naive, genotype 1 hepatitis C-infected patients. Hepatology. 2016;64(2):405–14. Epub 2016 Jun 7. PubMed PMID: 27115523.

    Article  PubMed  CAS  Google Scholar 

  22. Calleja JL, Crespo J, Rincón D, Ruiz-Antorán B, Fernandez I, Perelló C, Gea F, Lens S, García-Samaniego J, Sacristán B, García-Eliz M, Llerena S, Pascasio JM, Turnes J, Torras X, Morillas RM, Llaneras J, Serra MA, Diago M, Rodriguez CF, Ampuero J, Jorquera F, Simon MA, Arenas J, Navascues CA, Bañares R, Muñoz R, Albillos A, Mariño Z, Spanish Group for the Study of the Use of Direct-acting Drugs Hepatitis C Collaborating Group. Effectiveness, safety and clinical outcomes of direct-acting antiviral therapy in HCV genotype 1 infection: results from a Spanish real-world cohort. J Hepatol. 2017;66(6):1138–48. Epub 2017 Feb 9. PubMed PMID: 28189751.

    Article  PubMed  CAS  Google Scholar 

  23. Mariño Z, Pascasio-Acevedo JM, Gallego A, Diago M, Baliellas C, Morillas R, Prieto M, Moreno JM, Sánchez-Antolín G, Vergara M, Forné M, Fernández I, Castro MA, Pascual S, Gómez A, Castells L, Montero JL, Crespo J, Calleja JL, García-Samaniego J, Carrión JA, Arencibia AC, Blasco A, López-Núñez C, Sánchez-Ruano JJ, Gea-Rodríguez F, Giráldez Á, Cabezas J, Hontangas V, Torras X, Castellote J, Romero-Gómez M, Turnes J, de Artaza T, Narváez I, Cuervas-Mons V, Forns X. High efficacy of Sofosbuvir plus Simeprevir in a large cohort of Spanish cirrhotic patients infected with genotypes 1 and 4. Liver Int. 2017; [Epub ahead of print] PubMed PMID: 28481460.

  24. Siederdissen CH, Buggisch P, Boker K, Schott E, Klinker H, Pathil A, Pfeiffer-Vornkahl H, Berg T, Sarrazin C, Huppe D, Manns MP, Mauss S. Treatment of hepatitis C genotype 1 infection in Germany: effectiveness and safety of antiviral treatment in a real-world setting. United European Gastroenterol J. 2017;0(0):1–12.

    Article  Google Scholar 

  25. Ingiliz P, Christensen S, Kimhofer T, Hueppe D, Lutz T, Schewe K, Busch H, Schmutz G, Wehmeyer MH, Boesecke C, Simon KG, Berger F, Rockstroh JK, Zur Wiesch JS, Baumgarten A, Mauss S. Sofosbuvir and Ledipasvir for 8 weeks for the treatment of chronic hepatitis C virus (HCV) infection in HCV-Monoinfected and HIV-HCV-Coinfected individuals: results from the German hepatitis C cohort (GECCO-01). Clin Infect Dis. 2016;63(10):1320–4. Epub 2016 Aug 17. PubMed PMID: 27535952.

    Article  PubMed  CAS  Google Scholar 

  26. Kramer JR, Kanwal F, Richardson P, Mei M, El-Serag HB. Gaps in the achievement of effectiveness of HCV treatment in national VA practice. J Hepatol. 2012;56(2):320–5. Epub 2011 Jul 12. PubMed PMID: 21756855.

    Article  PubMed  Google Scholar 

  27. European Association for the Study of the Liver. EASL recommendations on treatment of hepatitis C 2014. J Hepatol. 2014;61(2):373–95. Epub 2014 May 10. PubMed PMID: 24818984.

    Article  Google Scholar 

  28. European Association for Study of Liver. EASL recommendations on treatment of hepatitis C 2015. J Hepatol. 2015;63(1):199–236. Epub 2015 Apr 21. PubMed PMID: 25911336.

    Article  Google Scholar 

  29. Poordad F, Schiff ER, Vierling JM, Landis C, Fontana RJ, Yang R, McPhee F, Hughes EA, Noviello S, Swenson ES. Daclatasvir with sofosbuvir and ribavirin for hepatitis C virus infection with advanced cirrhosis or post-liver transplantation recurrence. Hepatology. 2016;63(5):1493–505. Epub 2016 Mar 7. PubMed PMID: 26754432; PubMed Central PMCID: PMC5069651.

    Article  PubMed  CAS  Google Scholar 

  30. Alonso S, Riveiro-Barciela M, Fernandez I, Rincón D, Real Y, Llerena S, Gea F, Olveira A, Fernandez-Carrillo C, Polo B, Carrión JA, Gómez A, Devesa MJ, Baliellas C, Castro Á, Ampuero J, Granados R, Pascasio JM, Rubín A, Salmeron J, Badia E, Planas JM, Lens S, Turnes J, Montero JL, Buti M, Esteban R, Fernández-Rodríguez CM. Effectiveness and safety of sofosbuvir-based regimens plus an NS5A inhibitor for patients with HCV genotype 3 infection and cirrhosis. Results of a multicenter real-life cohort. J Viral Hepat. 2017;24(4):304–11. Epub 2016 Dec 9. PubMed PMID: 27935168.

    Article  PubMed  CAS  Google Scholar 

  31. Mücke MM, Mücke VT, Lange CM, Zeuzem S. Special populations: treating hepatitis C in patients with decompensated cirrhosis and/or advanced renal impairment. Liver Int. 2017;37(Suppl 1):19–25. Review. PubMed PMID: 28052635.

    Article  PubMed  Google Scholar 

  32. Reddy KR, Bourlière M, Sulkowski M, Omata M, Zeuzem S, Feld JJ, Lawitz E, Marcellin P, Welzel TM, Hyland R, Ding X, Yang J, Knox S, Pang P, Dvory-Sobol H, Subramanian GM, Symonds W, McHutchison JG, Mangia A, Gane E, Mizokami M, Pol S, Afdhal N. Ledipasvir and sofosbuvir in patients with genotype 1 hepatitis C virus infection and compensated cirrhosis: an integrated safety and efficacy analysis. Hepatology. 2015;62(1):79–86.

    Article  PubMed  CAS  Google Scholar 

  33. Bakr I, Rekacewicz C, El Hosseiny M, Ismail S, El Daly M, El-Kafrawy S, Esmat G, Hamid MA, Mohamed MK, Fontanet A. Higher clearance of hepatitis C virus infection in females compared with males. Gut. 2006;55(8):1183–7. Epub 2006 Jan 24. PubMed PMID: 16434426; PubMed Central PMCID: PMC1856273.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  34. Cavalcante LN, Lyra AC. Predictive factors associated with hepatitis C antiviral therapy response. World J Hepatol. 2015;7(12):1617–31. Review. PubMed PMID: 26140082; PubMed Central PMCID: PMC4483544.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Yu JW, Sun LJ, Zhao YH, Kang P, Yan BZ. Impact of gender on virologic response rates in genotype 1 chronic hepatitis C patients with peginterferon alpha-2a and ribavirin treatment. Int J Infect Dis. 2011;15(11):e740–6. Epub 2011 Jul 30. PubMed PMID: 21803628.

    Article  PubMed  CAS  Google Scholar 

  36. Floreani A, Cazzagon N, Boemo DG, Baldovin T, Baldo V, Egoue J, Antoniazzi S, Minola E. Female patients in fertile age with chronic hepatitis C, easy genotype, and persistently normal transaminases have a 100% chance to reach a sustained virological response. Eur J Gastroenterol Hepatol. 2011;23(11):997–1003. PubMed PMID: 21915057.

    Article  PubMed  Google Scholar 

  37. Villa E, Karampatou A, Cammà C, Di Leo A, Luongo M, Ferrari A, Petta S, Losi L, Taliani G, Trande P, Lei B, Graziosi A, Bernabucci V, Critelli R, Pazienza P, Rendina M, Antonelli A, Francavilla A. Early menopause is associated with lack of response to antiviral therapy in women with chronic hepatitis C. Gastroenterology. 2011;140(3):818–29. Epub 2010 Dec 16. PubMed PMID: 21167831.

    Article  PubMed  Google Scholar 

  38. Wehmeyer MH, Ingiliz P, Christensen S, Hueppe D, Lutz T, Simon KG, Schewe K, Boesecke C, Baumgarten A, Busch H, Rockstroh J, Schmutz G, Kimhofer T, Berger F, Mauss S, Wiesch JSZ. Real-world effectiveness of sofosbuvir-based treatment regimens for chronic hepatitis C genotype 3 infection: results from the multicenter German hepatitis C cohort (GECCO-03). J Med Virol. 2017; [Epub ahead of print] PubMed PMID: 28710853.

  39. Bischoff J, Mauss S, Cordes C, Lutz T, Scholten S, Moll A, Jäger H, Cornberg M, Manns MP, Baumgarten A, Rockstroh JK. Rates of sustained virological response 12 weeks after the scheduled end of direct-acting antiviral (DAA)-based hepatitis C virus (HCV) therapy from the National German HCV registry: does HIV coinfection impair the response to DAA combination therapy? HIV Med. 2018; [Epub ahead of print] PubMed PMID: 29368456.

  40. Berenguer J, Gil-Martin Á, Jarrin I, Moreno A, Dominguez L, Montes M, Aldámiz-Echevarría T, Téllez MJ, Santos I, Benitez L, Sanz J, Ryan P, Gaspar G, Alvarez B, Losa JE, Torres-Perea R, Barros C, San Martin JV, Arponen S, de Guzmán MT, Monsalvo R, Vegas A, Garcia-Benayas MT, Serrano R, Gotuzzo L, Menendez MA, Belda LM, Malmierca E, Calvo MJ, Cruz-Martos E, González-García JJ. All-oral DAA therapy against HCV in HIV/HCV-coinfected subjects in real-world practice: Madrid-CoRe findings. Hepatology. 2018; [Epub ahead of print] PubMed PMID: 29377274.

  41. Neukam K, Morano-Amado LE, Rivero-Juárez A, Mancebo M, Granados R, Téllez F, Collado A, Ríos MJ, de Los S-GI, Reus-Bañuls S, Vera-Méndez F, Geijo-Martínez P, Montero-Alonso M, Suárez-Santamaría M, Pineda JA. HIV-coinfected patients respond worse to direct-acting antiviral-based therapy against chronic hepatitis C in real life than HCV-monoinfected individuals: a prospective cohort study. HIV Clin Trials. 2017;18(3):126–34. PubMed PMID: 28599618.

    Article  PubMed  Google Scholar 

  42. Lionetti R, Calvaruso V, Piccolo P, Mancusi RL, Mazzarelli C, Fagiuoli S, Montalbano M, Lenci I, Carrai P, Guaraldi G, Visco-Comandini U, Milana M, Biolato M, Loiacono L, Valente G, Craxì A, Angelico M, D'offizi G. Sofosbuvir plus daclatasvir with or without ribavirin is safe and effective for post-transplant hepatitis C recurrence and severe fibrosis and cirrhosis: a prospective study. Clin Transpl. 2018;32(2) Epub 2017 Dec 18. PubMed PMID: 29193356.

  43. Welzel TM, Petersen J, Herzer K, Ferenci P, Gschwantler M, Wedemeyer H, Berg T, Spengler U, Weiland O, van der Valk M, Rockstroh J, Peck-Radosavljevic M, Zhao Y, Jimenez-Exposito MJ, Zeuzem S. Daclatasvir plus sofosbuvir, with or without ribavirin, achieved high sustained virological response rates in patients with HCV infection and advanced liver disease in a real-world cohort. Gut. 2016;65(11):1861–70. Epub 2016 Sep 7. Erratum in: Gut. 2016 Dec;65(12 ):2060. PubMed PMID: 27605539; PubMed Central PMCID: PMC5099229.

    Article  PubMed  CAS  Google Scholar 

  44. Cento V, Nguyen THT, Di Carlo D, Biliotti E, Gianserra L, Lenci I, Di Paolo D, Calvaruso V, Teti E, Cerrone M, Romagnoli D, Melis M, Danieli E, Menzaghi B, Polilli E, Siciliano M, Nicolini LA, Di Biagio A, Magni CF, Bolis M, Antonucci FP, Di Maio VC, Alfieri R, Sarmati L, Casalino P, Bernardini S, Micheli V, Rizzardini G, Parruti G, Quirino T, Puoti M, Babudieri S, D'Arminio Monforte A, Andreoni M, Craxì A, Angelico M, Pasquazzi C, Taliani G, Guedj J, Perno CF, Ceccherini-Silberstein F. Improvement of ALT decay kinetics by all-oral HCV treatment: Role of NS5A inhibitors and differences with IFN-based regimens. PLoS One. 2017;12(5):e0177352. eCollection 2017. PubMed PMID: 28545127; PubMed Central PMCID: PMC5436665.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  45. Welsch C, Efinger M, von Wagner M, Herrmann E, Zeuzem S, Welzel TM, Lange CM. Ongoing liver inflammation in patients with chronic hepatitis C and sustained virological response. PLoS One. 2017;12(2):e0171755. eCollection 2017. PubMed PMID: 28196130; PubMed Central PMCID: PMC5308806.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  46. Ippolito G, Zumla A, Lanini S. Is there sufficient evidence to repeal three decades of clinical research on chronic hepatitis C? Clin Microbiol Infect. 2018;24(4):328–31. Epub 2018 Jan 8. PubMed PMID: 29326009.

    Article  PubMed  CAS  Google Scholar 

Download references


Members of Lazio clinical network for DAA: C. Sarrecchia (Policlinico Tor Vergata, Roma); M. Pompili (Policlinico A. Gemelli, Roma); G.D’Ettorre (Policlinico Umberto I, Roma); C. Pasquazzi (Ospedale Sant’Andrea, Roma); R. Guarisco (Ospedale di Marino, Marino); M. Montalbano (INMI Spallanzani, Roma); E. Boumis (INMI Spallanzani, Roma); U. Visco-Comandini (INMI Spallanzani, Roma); M. Zaccarelli (INMI Spallanzani, Roma); A. Ammassari (INMI Spallanzani, Roma); R. Lionetti (INMI Spallanzani, Roma) S. Murachelli (INMI Spallanzani, Roma);I. MezzaRoma (Policlinico Umberto I, Roma);M D. Di Paolo (Policlinico Tor Vergata, Roma); C. Mastroianni (Ospedale Santa Maria Goretti, Latina); S. Francioso (Policlinico Tor Vergata, Roma); C. Puoti Ospedale di Marino, Marino); A. Grieco (Policlinico A. Gemelli, Roma); C. Furlan (Policlinico Umberto I, Roma); L. Loiacono (INMI Spallanzani, Roma); L. Fondacaro(San Camillo Forlanini, Roma) G. Cerasari (San Camillo Forlanini, Roma); D. Accapezzato (Policlinico Umberto I, Roma); G. Starnini (Ospedale Belcolle, Viterbo); M. Merili (Policlinico Umberto I, Roma) S. Corradini (Policlinico Umberto I, Roma); M. Lichtner (Ospedale Santa Maria Goretti, Latina); L. Ridola (Ospedale Santa Maria Goretti, Latina); A. Caterini (Ospedale Belcolle, Viterbo); E. Tamburrini (Policlinico A. Gemelli, Roma); R. Villani (San Camillo Forlanini Roma); L. Sarracino (Ospedale Fabrizio Spaziani, Frosinone); S. Sereno (Policlinico Umberto I, Roma); A: Brega (Policlinico Tor Vergata, Roma); A. Antinori (INMI Spallanzani, Roma); M. Marignani (Ospedale Sant’Andrea, Roma); I. Lenci (Policlinico Tor Vergata, Roma); C. Fimiani (Policlinico Umberto I, Roma); L. Sarmati (Policlinico Tor Vergata, Roma); R. Apaccini (Policlinico A. Gemelli, Roma); L. Spilabotti (Ospedale di Marino, Marino); T. Coluzzi (Ospedale Santa Maria Goretti, Latina); K. Casinelli (Ospedale Fabrizio Spaziani, Frosinone); F. Paoletti (Policlinico Umberto I, Roma); V. Mercurio (Ospedale Santa Maria Goretti, Latina); C. Mastropietro (Policlinico Umberto I, Roma); L. Miele (Policlinico A. Gemelli, Roma); P. Noto (INMI Spallanzani, Roma) A. Moretti (San Filippo Neri, Roma); P. Guarascio (San Camillo Forlanini, Roma); C.D’Ambrosio (San Camillo Forlanini, Roma); G.Labbadia (Policlinico Umberto I, Roma); C. Del Borgo (Ospedale Santa Maria Goretti, Latina); U. Vespasiani (Campus Biomedico, Roma); F. Palmieri (INMI Spallanzani, Roma); S. Cicalini (INMI Spallanzani; Roma) S. Cerilli (INMI Spallanzani, Roma); A. Sampaolesi (INMI Spallanzani, Roma); L. Vincenzi (INMI Spallanzani, Roma); R. Bellagamba (INMI Spallanzani, Roma); R. Cecere (Ospeale di Colleferro, Colleferro); V. Galati (INMI Spallanzani, Roma); A. Abdeddaim (INMI Spallanzani, Roma); G. Galati (Campus Biomedico, Roma); F. Iacomi (INMI Spallanzani, Roma); G. Iannicelli (INMI Spallanzani, Roma); G. Gentile Policlinico Umberto I, Roma); M. Bonaventura (Ospedale San Camillo de Lellis, Rieti); M. Scudieri (Ospedale San Camillo de Lellis, Rieti).


Lazio Region Health Authority and Ricerca Corrente del Ministero della Salute INMI-Spallanzani.

Availability of data and materials

Data are property of the Lazio Region Health Authority. The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Author information

Authors and Affiliations




Conceptualization: SL, PS, EG, LL, VP, AM, VPa, GI. Formal analysis: SL. Data extraction and administration of system: AM, FC. Patients care, investigation and data collection: VV, GT, ADS, AFA, CFP, AG, FC, GDO, AP, OA, FSM, AG, EG, MA, AA, MS. Methodology: SL, GI, PS, EG. Administration: AM, LL, FC, VPa. Supervision: GI, PS, AM. Writing original draft: SL, GI, PS. Writing, review and editing: all authors. All authors have read and approved the manuscript.

Corresponding author

Correspondence to Giuseppe Ippolito.

Ethics declarations

Ethics approval and consent to participate

This study was carried out within the institutional mandate of the Lazio Region Health Authority to the Lazio Regional Service for Epidemiology and Surveillance of Infectious Diseases (SeRESMI). The terms of SeRESMI mandate and utilization of data collected are established by a Regional law and includes monitoring access to therapy with DAA, monitoring therapy outcome and implementation of periodical analyses for administrative and scientific purposes. Patients signed informed consent for use of anonymous information accordingly with the Regional act which has enforced the clinical network. Patients’ data were collected through an on-line system and only physicians who have patients in care had access to patients’ personal information. Patients received treatment according to clinical judgment, current availability of drugs and current guidelines at the time they started therapy. We have received the consent for publishing the information contained in the study by the ethics committee of INMI Lazzaro Spallanzani.

Competing interests

CFP has received research grants, lecturing fees, advisory boards, scientific consultancies for Abbvie, Gilead Sciences, BMS, Janssen Cilag, VIIV, Roche, Abbott Diagnostics. EG has received personal fees from Gilead Sciences, Janssen, Otsuka Novel Products and Angelini for consultancy or lectures, outside the submitted work. GDO has received personal fees for Speaking, teaching and participation to advisory board for: Gilead, BMS, MSD. MA: has received grants for fellowship, research and participation to international meetings form Abbvie, Gilead, Janssen, MSD, he participated to advisory board for Gilead and Abbvie. GT: has received Traveling and speaking fees from Abbvie, BMS, Gilead, MSD. AP: has received grants for participation to meeting form: MSD, Gilead, Bristol Meyer Squibb. ADS: has received traveling and speaking fees from Abbvie and Gilead. AG: has received grants for fellowship, research and participation to international meetings form Abbvie, Gilead, Janssen, Alfa Wassermann, CD INV, Sigma Tau, Takeda, MSD; he participated to advisory board for Gilead, CD INV, Sigma Tau, Alfa Wassermann and Abbvie. FSM has received grants for fellowship, research and participation to international meetings form Abbvie, Gilead, Janssen, MSD; he participated to advisory board for Abbvie, Gilead, Janssen and MSD. GI, SL, VP, PS VV, MS, AM, LL, FC, OA, AFA, declare no competing interest.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Lanini, S., Scognamiglio, P., Mecozzi, A. et al. Impact of new DAA therapy on real clinical practice: a multicenter region-wide cohort study. BMC Infect Dis 18, 223 (2018).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: