Muzica CM, Stanciu C, Huiban L, Singeap AM, Sfarti C, Zenovia S, Cojocariu C, Trifan A. Hepatocellular carcinoma after direct-acting antiviral hepatitis C virus therapy: A debate near the end. World J Gastroenterol 2020; 26(43): 6770-6781 [PMID: 33268960 DOI: 10.3748/wjg.v26.i43.6770]
Corresponding Author of This Article
Anca Trifan, FRCP (C), MD, PhD, Doctor, Professor, Department of Gastroenterology, Grigore T. Popa University of Medicine and Pharmacy, St. Spiridon Emergency Hospital, University Street 16, Iasi 700115, Romania. email@example.com
Checklist of Responsibilities for the Scientific Editor of This Article
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Hepatocellular carcinoma after direct-acting antiviral hepatitis C virus therapy: A debate near the end
Cristina Maria Muzica, Carol Stanciu, Laura Huiban, Ana-Maria Singeap, Catalin Sfarti, Sebastian Zenovia, Camelia Cojocariu, Anca Trifan
Cristina Maria Muzica, Carol Stanciu, Laura Huiban, Ana-Maria Singeap, Catalin Sfarti, Sebastian Zenovia, Camelia Cojocariu, Anca Trifan, Department of Gastroenterology, Grigore T. Popa University of Medicine and Pharmacy, St. Spiridon Emergency Hospital, Iasi 700115, Romania
Author contributions: Trifan A, Stanciu C and Muzica CM contributed to conception and design of the study; Singeap AM, Cojocariu C and Huiban L were involved in the acquisition of data and contributed to the analysis and interpretation of data; Muzica CM, Zenovia S and Stanciu C drafted the manuscript; Sfarti C reviewed the paper; all authors have read and approved the final version of the manuscript; and all authors accept responsibility for its content.
Conflict-of-interest statement: Authors declare no conflict of interests for this article.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Anca Trifan, FRCP (C), MD, PhD, Doctor, Professor, Department of Gastroenterology, Grigore T. Popa University of Medicine and Pharmacy, St. Spiridon Emergency Hospital, University Street 16, Iasi 700115, Romania. firstname.lastname@example.org
Received: July 16, 2020 Peer-review started: July 16, 2020 First decision: September 14, 2020 Revised: September 27, 2020 Accepted: October 20, 2020 Article in press: October 20, 2020 Published online: November 21, 2020
Direct acting antivirals (DAAs) have revolutionized the treatment of hepatitis C virus (HCV) infection, achieving high rates (≥ 95%) of sustained virological response, with a good safety profile and high compliance rates. Consequently, it had been expected that viral clearance will reduce morbidity and mortality rates, as well as the risk of hepatocellular carcinoma (HCC). However, since 2016, concerns have been raised over an unexpected high rate of HCC occurrence and recurrence after DAA therapy, which led to an avalanche of studies with contradictory results. We aimed to review the most recent and relevant articles regarding the risk of HCC after DAA treatment and identify the associated risk factors.
Core Tip: The risk of hepatocellular carcinoma (HCC) occurrence or recurrence in patients with chronic hepatitis C virus (HCV) infection receiving direct acting antivirals (DAAs) has been debated through the last 4 years. Data provided by current literature indicate a decreasing incidence rate of HCC (both de novo and recurrent) in patients with chronic hepatitis C, HCV-related cirrhosis, and HCV-related HCC after achieving sustained virological response with DAAs.
Citation: Muzica CM, Stanciu C, Huiban L, Singeap AM, Sfarti C, Zenovia S, Cojocariu C, Trifan A. Hepatocellular carcinoma after direct-acting antiviral hepatitis C virus therapy: A debate near the end. World J Gastroenterol 2020; 26(43): 6770-6781
Hepatocellular carcinoma (HCC) represents the most frequent histologic type among primary liver neoplasia, and is the fifth most common cancer globally comprising 5.6% of all cancers and the second most common cause of cancer death. The leading risk factor for HCC is chronic hepatitis C virus (HCV) infection with a 3% annual risk in patients with HCV liver cirrhosis. Data from WHO’s global hepatitis report shows that 1% of the world population is infected with HCV. Beside inducing liver injury and fibrosis which subsequently will lead to liver cirrhosis, HCV has a direct carcinogenic potential with pro-oncogenic effects upon the infected cell through oxidative stress, DNA damage and deregulation of host cell checkpoints.
Most studies regarding the risk of HCC in patients with HCV chronic infection treated with interferon (IFN)-based therapy reported that achieving sustained viral response (SVR) reduced the risk to 0.5%-1% per year[5,6]. However, IFN-based therapy was limited by a low SVR rate (approximately 40%-50%) and a poor tolerance among patients with cirrhosis due to multiple adverse events.
The therapy of HCV infection was revolutionized by the introduction of the currently approved IFN-free regimens containing all-oral direct-acting antivirals (DAAs) which target viral proteins such as NS3/4A protease, NS5B polymerase and the NS5A replication complex, achieving SVR rates in over 95% of patients, with good safety profile and excellent tolerance[8-10]. Thus, it was expected that viral clearance will reduce morbidity and mortality rates implying a decreased risk of HCC. Several studies which assessed the risk of HCC occurrence and recurrence in patients treated with IFN-based therapy, have shown that the risk is significantly lower in those who achieved a SVR than in those who did not. In addition, SVR-achieving patients benefit from long-term preserved liver function and consequently a longer survival. However, data provided by 2 studies published in 2016 were a matter of concern regarding the high risk of HCC occurrence and recurrence after DAA therapies[13,14]. The debate was continued by several studies reporting conflicting data and thus casting a shadow over the relation between DAA therapy and HCC. Although it is commonly known that the risk of HCC remains even after HCV clearance, it is important to clarify whether DAAs have a role in suppressing the development of HCC.
We carried out a review of the most recent and relevant articles regarding the risk of HCC after DAA therapy and identify the associated risk factors.
THE RELATION BETWEEN HCC AND CHRONIC HCV INFECTION
Commonly, HCC develops in a liver with histologic abnormalities, the presence of chronic liver disease representing a potential risk for tumour initiation and progression. In about 90% of the cases, HCC is associated with a known risk factor. The most important risk factor for the development of HCC is liver cirrhosis of whatever etiology, which is considered a premalignant lesion and is present in over 70% of cases. Liver cirrhosis marks the final stage of all chronic hepatopathies and the most common causes are chronic infection with HBV or HCV, alcohol consumption, hereditary metabolic diseases such as hemochromatosis or alpha-1-antitrypsin deficiency and non-alcoholic steatohepatitis. All etiologic forms of cirrhosis may be complicated by the development of HCC, but patients with chronic HBV and HCV infection are under a higher risk.
HCV is an RNA virus that belongs to the Flaviviridae family, consisting of single-stranded RNA whose genome encodes a protein comprising 3000 amino acids from which, via proteolysis, result structural and nonstructural proteins. Structural proteins (core, envelope E1 and E2) play an important role in determining the morphological viral characteristics and in the invasion process of host-cells. Nonstructural proteins (P1, NS2, NS3, NS4A, NS4B, NS5A and NS5B) are involved in viral replication and the pathogenesis of secondary liver injury. The HCV genome is very heterogeneous with at least seven genotypes and several subtypes reported so far. HCV genotype 1, 3 and 6 have been incriminated in a poor clinical outcome as compared to the other genotypes, with a higher prevalence of cirrhosis or HCC[18-20]. The hepatocarcinogenesis induced by chronic HCV infection is a multistage and multifactorial process, in which direct and indirect mechanisms interact leading to the creation of a pro-carcinogenic microenvironment represented by liver cirrhosis, in which viral protein structures act as promoters of malignant degeneration. HCC development due to HCV is a gradual process spanning two to four decades. HCV carcinogenesis is mediated by viral-induced factors and host immunologic response which is mediated by tumoral necrosis factor, IFNs and chronic inflammation secondary to HCV. Cell cycles are associated with mutations that can transform hepatocytes to malignant cells. Telomerase reverse transcriptase, tumour protein 53, β catenin are the most frequent genes mutated in HCC.
HCC OCCURRENCE AFTER DAA THERAPY
IFN-based therapy provided undisputed clinical benefit in pre-cirrhotic and cirrhotic SVR-achieving patients, with a significant reduction in disease progression and complications, including HCC when compared to those without SVR or untreated[11,25-27]. The risk factors associated with HCC development in IFN-treated patients achieving SVR are older age, male gender, advanced liver fibrosis, fatty liver, and a high posttreatment serum alpha-fetoprotein (AFP) level[28-30]. However, due to restrictive inclusion criteria, low SVR rates and high treatment-related toxicity, IFN-based therapy was not an ideal treatment in patients with chronic HCV infection.
The IFN-free regimens using new DAAs represent a turning point in the treatment of patients with chronic HCV infection, providing high SVR rates and fair tolerance, which raised the expectations of preventing complications of advanced liver disease in HCV patients, including HCC. These prospects are based on data provided by previous studies carried out in the IFN era, demonstrating a decline in HCC incidence in SVR-achieving patients[31,32]. Nonetheless, despite evidences that achieving SVR provide protection against HCC development, several articles published in 2016 and 2017 reported an unexpected increased occurrence, recurrence and a more aggressive pattern of HCC after DAA therapy in cirrhotic HCV patients[13,14,33]. The results of these studies were countered by many because of the small cohort size, the absence of control groups, and short follow-up periods (Table 1).
Table 1De novo hepatocellular carcinoma incidence after direct-acting antiviral treatment.
DAA: Direct-acting antivirals; SOT: Start of treatment; FU: Follow-up; HCC: Hepatocellular carcinoma; HCV: Hepatitis C virus; IFN: Interferon; IQR: Interquartile range; PY: Person-year; EOT: End of treatment; SVR: Sustained viral response.
Retrospective studies comparing outcomes after DAAs vs IFN-based therapy
A large cohort study which compared 30183 DAA-treated patients to 137502 patients without evidence of HCV treatment and 12948 IFN-treated patients, identified a more advanced age, predominance of male sex and cirrhosis at baseline in DAA-treated patients compared to those untreated. After adjustments for variables, the authors reported a significantly reduced risk of HCC relative to no treatment (adjusted HR = 0.84, 95%CI: 0.73-0.96), and relative to IFN-based treatment (HR = 0.69, 95%CI: 0.59-0.81). Similarly, Ioannou et al conducted a study in which 60000 patients with antiviral treatment were enrolled between 1999 and 2015. The antiviral regimens were divided into 3 groups: 35871 IFN-only, 4535 DAA and IFN, and 21948 DAA-only with a mean follow-up time of 6.1 years for all patients and 1.53 years for the DAA-only group. The study found a significant reduction in HCC occurrence risk of 71% (adjusted HR = 0.29; 95%CI: 0.23-0.37) in patients with DAA-induced SVR. Janjua et al recently published a study which evaluated a large cohort treated with DAAs compared with a retrospective cohort treated with IFN. The authors found a similar rate reduction in HCC risk in patients who achieved SVR obtained either with DAAs or with IFN-based regimens (70% reduction for DAAs and 79% for IFN-based therapy).
Retrospective studies assessing outcomes after DAAs
Kanwal et al conducted a cohort study which evaluated the risk of HCC in 22500 DAA-treated patients with a mean follow-up period of 1.02 years. The study demonstrated that the risk of HCC in patients with SVR is significantly reduced as compared with non-SVR patients [0.90 vs 3.45 HCC/100 person year (PY); adjusted HR = 0.28, 95%CI: 0.22-0.36]. Similarly, in a study including almost 4000 DAA-treated HCV patients from several centers across Spain, Calleja et al aimed to evaluate the effectiveness, safety and clinical outcomes of DAA-based therapy in HCV genotype 1 infection, reported a HCC incidence of 0.93% within 18 mo of starting DAAs treatment with ombitasvir/paritaprevir/ritonavir plus dasabuvir (OMV/PTV/r+DSV) and ledipasvir/sofosbuvir (LDV/SOF). It should be mentioned that measuring the incidence of HCC was not an objective of this study. In contrast to these results, the same team that had previously reported a reduced risk of HCC in patients with chronic HCV infection treated with DAAs, recently published another retrospective cohort study in which evaluated the long-term risk of HCC in patients with SVR to DAAs, followed up for over 3.5 years after SVR. From 18076 patients who achieved SVR with DAAs, they found 544 patients with de novo HCC, with 1-, 2-, and 3-year cumulative risks of HCC of 1.1%, 1.9% and 2.8%, respectively. Results from another two recently published studies are consistent with those reported by this second study by Kanwal et al In a retrospective study, Tani et al demonstrated that the 12- and 36-mo cumulative incidences of HCC were 1.88 and 6.00%, respectively. Similarly, Watanabe et al reported 1- and 2-year cumulative incidences of HCC of 1.9 and 4.1%, respectively.
A prospective study by Cheung et al which included 406 patients with decompensated cirrhosis found no evidence of an increased risk for HCC during DAA therapy or during the 12-mo follow-up. The authors found a 4.2% HCC incidence in the first six months from the start of DAA treatment, the equivalent to the occurrence seen in a matched control group containing untreated patients. Furthermore, the authors suggested the possibility of pre-existing undiagnosed cancer in patients which developed HCC during DAA treatment. Another large prospective study from ANRS CO12 CirVir cohort including 1270 HCV patients with compensated biopsy-proven cirrhosis reported that after Cox analysis there was no statistically significant increase in the risk of HCC development associated with DAAs use. A large prospective study by Mettke et al containing 158 HCV-related cirrhotic patients treated with DAAs and 184 HCV-related cirrhotic patients without treatment, demonstrated a similar HCC incidence over a short period of time in the two groups (HCC developed in 6 DAA-treated patients and 14 untreated patients, yielding HCC incidence rates of 2.90 and 4.48 per 100 person-years, respectively). A multi-center prospective cohort study published by Carrat et al in France also found that treatment with DAAs was associated with a reduced risk for mortality and HCC. The study included 7344 patients with DAA treatment and 2551 patients without treatment, with a mean follow-up period of 33.4 mo. After adjustment for variables, DAA treatment was associated with a decrease in HCC (adjusted HR = 0.66, 95%CI: 0.46-0.91) and all-cause mortality (adjusted HR = 0.48, 95%CI: 0.33-0.70). Also, recent results from the ongoing phase 3b trials TOPAZ-I and TOPAZ-II demonstrated a low incidence rate of HCC in DAA-treated HCV patients. The combined interim results from both the TOPAZ-I and TOPAZ-II studies performed up to 156 wk posttreatment showed that the rates of liver transplantation, liver decompensation, HCC and liver-related death were 0.6%, 2.0%, 1.4%, and 0.3%, respectively. Another recent prospective study by Sangiovanni et al, including 1285 consecutive patients with HCV-related cirrhosis without any history of HCC (group 1), and 124 cirrhotics with previous HCC and compete response to treatment (group 2) found an yearly incidence of 3.1/100 PY-recent data from a prospective study by Romano et al showed a HCC incidence rate of 0.97 per 100 PY (95%CI: 0.73-1.26) and a sharp decline in HCC risk in the 2nd year of follow-up in patients with HCV-related cirrhosis treated with DAAs.
Ma et al recently published a large meta-analysis in which 276848 HCV-infected patients treated either with IFN-based therapy or with DAAs were included. The authors reported that DAA treatment is not better than IFN-based therapies in preventing the development of HCC, indicating that IFN-based therapy might currently be irreplaceable in the prophylaxis of HCC in patients with chronic hepatitis C.
HCC RECURRENCE AFTER DAA THERAPY
In patients with early disease stage HCC - Barcelona Clinic Liver Cancer Stage 0/A – BCLC 0/A, there are available potentially curative treatments such as surgical resection and local ablation, with high 5-year overall survival rate. However, tumour recurrence and decompensation of underlying cirrhosis contribute to long-term mortality even after curative treatment. As stated by previous research, HCC recurrence after an initial complete response may develop through either the dissemination of cells from the original tumor prior to curative therapy, or through de-novo cancers arising in the cirrhotic genetically altered microenviroment. Thus, it seems appropriate to stratify the recurrence of HCC into: (1) Intra-hepatic metastasis of the original tumor; and (2) Multicentric carcinogenesis. The distinction between these models is mandatory and it could be made using the amount of time between curative therapy and recurrence. Thereby, an early recurrence within 1-2 years may be attributed to intrahepatic metastasis, whereas a recurrence > 2 years is supposedly due to metachronous HCC. Microscopic vascular invasion and/or satellites are high risk hallmarks for dissemination whilst sustained inflammation with persistent liver damage is predictive for multicentric carcinogenesis/metachronic tumors. The most important factor in predicting the growth of nested malignant cell from the primary tumor is the immune cancer surveillance which in a normal setting triggers the activation of stromal cells and lymphocyte recruitment, secondary leading to the suppression of cell clones. Several studies from the IFN era highlighted the beneficial effect on HCC recurrence exerted by IFN-based therapy[54-57]. One of the major differences between IFN and DAA obtained SVR is the kinetics of viral suppression which may be the key in explaining the high recurrence rate of HCC. The mechanism proposed for HCC recurrence in patients with SVR obtained with DAAs in prior HCV-related HCC patients, consists of a disruption of the immune cancer surveillance due to an abrupt resolution of a chronic inflammatory state as the suppression of HCV replication occurs in the first days after therapy.
However, available data regarding HCC recurrence in patients with initial complete response to hepatic resection or local ablation following DAA-induced SVR are scarce and conflicting (Table 2).
Table 2 Recurrent hepatocellular carcinoma incidence after direct-acting antiviral treatment.
In 2016, Reig et al reported an unexpected high rate of 27.6% of early tumor recurrence in patients with HCV-related HCC undergoing DAA treatment. Similar results were found by Conti et al in a single-center retrospective cohort study, with a recurrence rate of HCC after DAAs of 28.81%. Contrasting results were reported by Lin et al in a recently published retrospective study which included 107 patients with HCV-related HCC, of whom 60 received DAA therapy after treatment for HCC. After a median follow-up of 20 mo, 37.1% patients had HCC recurrence after DAAs. The authors concluded that, compared to untreated patients, DAA therapy did not increase recurrent HCC after curative treatment and also improved the survival outcome of HCC patients. In line with these results, the largest retrospective cohort study ever reported was recently published, including untreated control arm, based on 31 health systems throughout the United States and Canada. The study included 793 HCV-related HCC patients of which 304 (38.3%) received DAA therapy and 489 (61.7%) were untreated. The rate of tumor recurrence was 42.1% in DAA-treated patients and 58.9% in the untreated group. After variable adjustments, the study reported that DAA exposure is not associated with an increased risk of HCC recurrence (HR = 0.90; 95%CI: 0.70-1.16). A meta-analysis published by Lui et al also showed that the use of DAA therapy is associated with a significantly lower risk of HCC development compared to patients without DAA treatment. The authors found a > 60% lower risk of HCC recurrence in patients exposed to DAA compared to controls (OR = 0.36, 95%CI: 0.27-0.47; P < 0.001; I2 = 88%).
A retrospective cohort study which compared outcomes of patients with prior HCV-related HCC treated with DAAs vs IFN-based therapy found no significant difference between IFN-based and IFN-free therapy groups by propensity score-matched analysis (5-year incidence; 54.2% in IFN-based, 45.1% in IFN-free therapy; P = 0.54). Consistent with these findings, results from a recent retrospective cohort from Japan showed that SVR by therapy with DAAs exhibited an anti-liver tumorigenesis effect equal to that of IFN-based therapy and reduced the risk of HCC recurrence (P = 0.564).
A prospective multicenter French study that included ANRS cohorts concluded that the rate of HCC recurrence was not different between DAA-treated and untreated groups. Cabibbo et al conducted a prospective multicenter study in Italy in which were included 143 patients with successfully treated BCLC 0/A HCC, and subsequently treated with DAAs. They found an HCC-recurrence incidence of 12%, 26.6%, and 29.1%, respectively in 6-, 12-, and 18-mo of follow-up, and concluded that although the risk of HCC recurrence remains high, it is comparable between the DAA group and the untreated group.
RISK FACTORS FOR DE NOVO AND RECURRENT HCC
The increasing number of patients who will obtain HCV clearance with DAAs and the continued risk of hepatocarcinogenesis even after SVR require the identification of patients at highest risk of developing HCC. Regarding the host risk factors such as older age, male gender and family history, HBV or HIV co-infection, alcohol consumption, steatohepatitis and advanced liver disease are well known as associated risk factors. Also, tobacco smoking and exposure to aflatoxin are the most studied environmental risk factors involved in the development of HCC. The risk factors incriminated in HCC occurrence and recurrence, in patients treated with DAAs, are mainly older age, non-SVR and advanced liver disease (Table 3).
Table 3 Risk factors for de novo and recurrent hepatocellular carcinoma after direct-acting antiviral therapy.
A study conducted by Kanwal et al which included DAA treated patients, reported a 4.7-fold higher HCC risk in cirrhotic patients than in those without cirrhosis (adjusted HR = 4.73; 95%CI: 3.34-6.68). Similar findings were disclosed by Ioannou et al in a large cohort retrospective study, concluding that the incidence of HCC was highest in patients with cirrhosis and treatment failure. Singer et al demonstrated that older age, male gender, liver cirrhosis, thrombocytopenia, portal hypertension, diabetes, tobacco use, alcoholic liver disease, and use of betablockers and anti-hypertensives were associated with an increased risk of HCC in multivariable adjusted models. Despite using different inclusion criteria and study methods, these three cohort studies demonstrated that the presence of cirrhosis and the absence of SVR were the major risk factors of HCC occurrence in HCV patients[34,35,37]. A high FIB-4 index and posttreatment AFP were identified as independent factors that contributed to HCC occurrence in two recent studies[39,41].
In the 2016 paper, Conti et al reported that decompensated cirrhosis characterized by a high Child-Pugh-Turcotte score (OR = 4.18, 95%CI: 1.17-14.8, P = 0.03) and a history of HCC (OR = 12.0, 95%CI: 4.02-35.74, P < 0.0001) were associated with HCC. In addition, a large comparative study from Japan revealed that posttreatment Wisteria floribunda agglutinin positive Mac-2 binding protein (WFA+M2BP) was significantly associated with HCC recurrence in patients with HCV without advanced liver fibrosis. In addition, the comparative study for occurrence and recurrence of HCC in IFN-based vs DAAs, showed that AFP (> 5.4 ng/mL) and WFA+M2BP levels (> 1.8 COI) were strongly associated with de novo HCC in those with DAA therapy. In a recently published retrospective study, Sangiovanni et al found at multivariable Cox regression models that ascites and AFP log-value were independently associated with HCC occurrence, while a history of alcohol abuse and HCC recurrence was associated with HCC recurrence.
In addition to these findings from retrospective studies, Ide et al found that besides male gender and an older age, higher FIB-4 index and GGTP levels, were independently associated with HCC occurrence. Also, Calvaruso et al found in their prospective study that albumin level (< 3.5 g/dL), platelets < 120 × 109/L and failure to achieve SVR were associated with an increased risk of HCC development. The failure in achieving SVR was also incriminated as a risk factor for HCC occurrence along with HBV coinfection and APRI > 2.5, in another study from Italy. Another study which enrolled patients with a history of successful radiofrequency ablation treatment for HCV-related HCC who had received antiviral therapy with DAAs (147 patients) or IFN (156 patients) reported that a higher AFP-L3 level, larger number of HCC treatments, and a shorter interval between the last HCC treatment and the initiation of antiviral therapy were associated with the risk of HCC recurrence. A recent study from Egipt, which enrolled 160 DAA-treated and 80 untreated HCV patients, showed that an ultrasound measured adequate liver volume (at a cutoff of 495 mL) predicted HCC occurrence after DAAs.
Most of the studies we reviewed indicated that the major risk factors for HCC occurrence and recurrence are male gender, older age, non-SVR, advanced liver fibrosis and higher post-treatment AFP levels, in agreement with those identified by prior studies of the IFN era[25,72].
Data provided by the most recent and relevant articles sustain a reduced incidence rate of both de novo and recurrent HCC after achieving SVR with DAA therapy, therefore we consider that the debate regarding the impact of DAAs on HCC risk is drawing to an end.
World Health Organization.
Global hepatitis report, 2017. April 2017 [cited 9 January 2020]. Available from: https://www.who.int/hepatitis/publications/global-hepatitis-report2017/en/.
[PubMed] [DOI][Cited in This Article: ]
Bourlière M, Bronowicki JP, de Ledinghen V, Hézode C, Zoulim F, Mathurin P, Tran A, Larrey DG, Ratziu V, Alric L, Hyland RH, Jiang D, Doehle B, Pang PS, Symonds WT, Subramanian GM, McHutchison JG, Marcellin P, Habersetzer F, Guyader D, Grangé JD, Loustaud-Ratti V, Serfaty L, Metivier S, Leroy V, Abergel A, Pol S. Ledipasvir-sofosbuvir with or without ribavirin to treat patients with HCV genotype 1 infection and cirrhosis non-responsive to previous protease-inhibitor therapy: a randomised, double-blind, phase 2 trial (SIRIUS).Lancet Infect Dis. 2015;15:397-404.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 219][Cited by in F6Publishing: 88][Article Influence: 36.5][Reference Citation Analysis (0)]
Charlton M, Everson GT, Flamm SL, Kumar P, Landis C, Brown RS Jr, Fried MW, Terrault NA, O'Leary JG, Vargas HE, Kuo A, Schiff E, Sulkowski MS, Gilroy R, Watt KD, Brown K, Kwo P, Pungpapong S, Korenblat KM, Muir AJ, Teperman L, Fontana RJ, Denning J, Arterburn S, Dvory-Sobol H, Brandt-Sarif T, Pang PS, McHutchison JG, Reddy KR, Afdhal N; SOLAR-1 Investigators. Ledipasvir and Sofosbuvir Plus Ribavirin for Treatment of HCV Infection in Patients With Advanced Liver Disease.Gastroenterology. 2015;149:649-659.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 580][Cited by in F6Publishing: 519][Article Influence: 96.7][Reference Citation Analysis (0)]
Cabibbo G, Celsa C, Calvaruso V, Petta S, Cacciola I, Cannavò MR, Madonia S, Rossi M, Magro B, Rini F, Distefano M, Larocca L, Prestileo T, Malizia G, Bertino G, Benanti F, Licata A, Scalisi I, Mazzola G, Di Rosolini MA, Alaimo G, Averna A, Cartabellotta F, Alessi N, Guastella S, Russello M, Scifo G, Squadrito G, Raimondo G, Trevisani F, Craxì A, Di Marco V, Cammà C; Rete Sicilia Selezione Terapia – HCV (RESIST-HCV) and Italian Liver Cancer (ITA. LI.CA.) Group. Direct-acting antivirals after successful treatment of early hepatocellular carcinoma improve survival in HCV-cirrhotic patients.J Hepatol. 2019;71:265-273.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 56][Cited by in F6Publishing: 59][Article Influence: 28.0][Reference Citation Analysis (0)]
Preda CM, Popescu CP, Baicus C, Voiosu TA, Manuc M, Pop CS, Gheorghe L, Sporea I, Trifan A, Tantau M, Tantau A, Ceausu E, Proca D, Constantinescu I, Ruta SM, Diculescu MM, Oproiu A. Real-world efficacy and safety of ombitasvir, paritaprevir/r+dasabuvir+ribavirin in genotype 1b patients with hepatitis C virus cirrhosis.Liver Int. 2018;38:602-610.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 12][Cited by in F6Publishing: 14][Article Influence: 3.0][Reference Citation Analysis (0)]
Innes HA, McDonald SA, Dillon JF, Allen S, Hayes PC, Goldberg D, Mills PR, Barclay ST, Wilks D, Valerio H, Fox R, Bhattacharyya D, Kennedy N, Morris J, Fraser A, Stanley AJ, Bramley P, Hutchinson SJ. Toward a more complete understanding of the association between a hepatitis C sustained viral response and cause-specific outcomes.Hepatology. 2015;62:355-364.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 77][Cited by in F6Publishing: 80][Article Influence: 12.8][Reference Citation Analysis (0)]
Oze T, Hiramatsu N, Yakushijin T, Miyazaki M, Yamada A, Oshita M, Hagiwara H, Mita E, Ito T, Fukui H, Inui Y, Hijioka T, Inada M, Katayama K, Tamura S, Yoshihara H, Inoue A, Imai Y, Hayashi E, Kato M, Miyagi T, Yoshida Y, Tatsumi T, Kasahara A, Hamasaki T, Hayashi N, Takehara T; Osaka Liver Forum. Post-treatment levels of α-fetoprotein predict incidence of hepatocellular carcinoma after interferon therapy.Clin Gastroenterol Hepatol. 2014;12:1186-1195.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 65][Cited by in F6Publishing: 60][Article Influence: 8.1][Reference Citation Analysis (0)]
van der Meer AJ, Veldt BJ, Feld JJ, Wedemeyer H, Dufour JF, Lammert F, Duarte-Rojo A, Heathcote EJ, Manns MP, Kuske L, Zeuzem S, Hofmann WP, de Knegt RJ, Hansen BE, Janssen HL. Association between sustained virological response and all-cause mortality among patients with chronic hepatitis C and advanced hepatic fibrosis.JAMA. 2012;308:2584-2593.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 1051][Cited by in F6Publishing: 958][Article Influence: 131.4][Reference Citation Analysis (0)]
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;66:1138-1148.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 113][Cited by in F6Publishing: 104][Article Influence: 28.3][Reference Citation Analysis (0)]
Tani J, Morishita A, Sakamoto T, Takuma K, Nakahara M, Fujita K, Oura K, Tadokoro T, Mimura S, Nomura T, Yoneyama H, Kobara H, Himoto T, Tsutsui A, Senoh T, Nagano T, Ogawa C, Moriya A, Deguchi A, Takaguchi K, Masaki T. Simple scoring system for prediction of hepatocellular carcinoma occurrence after hepatitis C virus eradication by direct-acting antiviral treatment: All Kagawa Liver Disease Group Study.Oncol Lett. 2020;19:2205-2212.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 5][Cited by in F6Publishing: 8][Article Influence: 5.0][Reference Citation Analysis (0)]
Carrat F, Fontaine H, Dorival C, Simony M, Diallo A, Hezode C, De Ledinghen V, Larrey D, Haour G, Bronowicki JP, Zoulim F, Asselah T, Marcellin P, Thabut D, Leroy V, Tran A, Habersetzer F, Samuel D, Guyader D, Chazouilleres O, Mathurin P, Metivier S, Alric L, Riachi G, Gournay J, Abergel A, Cales P, Ganne N, Loustaud-Ratti V, D'Alteroche L, Causse X, Geist C, Minello A, Rosa I, Gelu-Simeon M, Portal I, Raffi F, Bourliere M, Pol S; French ANRS CO22 Hepather cohort. Clinical outcomes in patients with chronic hepatitis C after direct-acting antiviral treatment: a prospective cohort study.Lancet. 2019;393:1453-1464.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 207][Cited by in F6Publishing: 77][Article Influence: 103.5][Reference Citation Analysis (0)]
Poordad F, Castro RE, Asatryan A, Aguilar H, Cacoub P, Dieterich D, Marinho RT, Carvalho A, Siddique A, Hu YB, Charafeddine M, Bondin M, Khan N, Cohen DE, Felizarta F. Long-term safety and efficacy results in hepatitis C virus genotype 1-infected patients receiving ombitasvir/paritaprevir/ritonavir + dasabuvir ± ribavirin in the TOPAZ-I and TOPAZ-II trials.J Viral Hepat. 2020;27:497-504.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 4][Cited by in F6Publishing: 3][Article Influence: 4.0][Reference Citation Analysis (0)]
Sangiovanni A, Alimenti E, Gattai R, Filomia R, Parente E, Valenti L, Marzi L, Pellegatta G, Borgia G, Gambato M, Terreni N, Serio I, Belli L, Oliveri F, Maimone S, Brunacci M, D'Ambrosio R, Forzenigo LV, Russo FP, Rumi M, Barone M, Fracanzani AL, Raimondo G, Giannini EG, Brunetto MR, Villa E, Biganzoli E, Colombo M, Lampertico P. Undefined/non-malignant hepatic nodules are associated with early occurrence of HCC in DAA-treated patients with HCV-related cirrhosis.J Hepatol. 2020;73:593-602.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 13][Cited by in F6Publishing: 15][Article Influence: 13.0][Reference Citation Analysis (0)]
Romano A, Angeli P, Piovesan S, Noventa F, Anastassopoulos G, Chemello L, Cavalletto L, Gambato M, Russo FP, Burra P, Vincenzi V, Scotton PG, Panese S, Tempesta D, Bertin T, Carrara M, Carlotto A, Capra F, Carolo G, Scroccaro G, Alberti A. Newly diagnosed hepatocellular carcinoma in patients with advanced hepatitis C treated with DAAs: A prospective population study.J Hepatol. 2018;69:345-352.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 66][Cited by in F6Publishing: 67][Article Influence: 22.0][Reference Citation Analysis (0)]
Singal AG, Rich NE, Mehta N, Branch A, Pillai A, Hoteit M, Volk M, Odewole M, Scaglione S, Guy J, Said A, Feld JJ, John BV, Frenette C, Mantry P, Rangnekar AS, Oloruntoba O, Leise M, Jou JH, Bhamidimarri KR, Kulik L, Tran T, Samant H, Dhanasekaran R, Duarte-Rojo A, Salgia R, Eswaran S, Jalal P, Flores A, Satapathy SK, Wong R, Huang A, Misra S, Schwartz M, Mitrani R, Nakka S, Noureddine W, Ho C, Konjeti VR, Dao A, Nelson K, Delarosa K, Rahim U, Mavuram M, Xie JJ, Murphy CC, Parikh ND. Direct-Acting Antiviral Therapy Not Associated With Recurrence of Hepatocellular Carcinoma in a Multicenter North American Cohort Study. Gastroenterology 2019; 156: 1683-1692.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 66][Cited by in F6Publishing: 60][Article Influence: 33.0][Reference Citation Analysis (0)]
Nagata H, Nakagawa M, Asahina Y, Sato A, Asano Y, Tsunoda T, Miyoshi M, Kaneko S, Otani S, Kawai-Kitahata F, Murakawa M, Nitta S, Itsui Y, Azuma S, Kakinuma S, Nouchi T, Sakai H, Tomita M, Watanabe M; Ochanomizu Liver Conference Study Group. Effect of interferon-based and -free therapy on early occurrence and recurrence of hepatocellular carcinoma in chronic hepatitis C.J Hepatol. 2017;67:933-939.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 117][Cited by in F6Publishing: 113][Article Influence: 29.3][Reference Citation Analysis (0)]
Cabibbo G, Petta S, Calvaruso V, Cacciola I, Cannavò MR, Madonia S, Distefano M, Larocca L, Prestileo T, Tinè F, Bertino G, Giannitrapani L, Benanti F, Licata A, Scalisi I, Mazzola G, Cartabellotta F, Alessi N, Barbàra M, Russello M, Scifo G, Squadrito G, Raimondo G, Craxì A, Di Marco V, Cammà C; Rete Sicilia Selezione Terapia - HCV (RESIST-HCV). Is early recurrence of hepatocellular carcinoma in HCV cirrhotic patients affected by treatment with direct-acting antivirals?Aliment Pharmacol Ther. 2017;46:688-695.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 92][Cited by in F6Publishing: 85][Article Influence: 23.0][Reference Citation Analysis (0)]
Ide T, Koga H, Nakano M, Hashimoto S, Yatsuhashi H, Higuchi N, Nakamuta M, Oeda S, Eguchi Y, Shakado S, Sakisaka S, Yoshimaru Y, Sasaki Y, Honma Y, Harada M, Seike M, Maeshiro T, Miuma S, Nakao K, Mawatari S, Ido A, Nagata K, Matsumoto S, Takami Y, Sohda T, Kakuma T, Torimura T. Direct-acting antiviral agents do not increase the incidence of hepatocellular carcinoma development: a prospective, multicenter study.Hepatol Int. 2019;13:293-301.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 15][Cited by in F6Publishing: 17][Article Influence: 7.5][Reference Citation Analysis (0)]
Calvaruso V, Cabibbo G, Cacciola I, Petta S, Madonia S, Bellia A, Tinè F, Distefano M, Licata A, Giannitrapani L, Prestileo T, Mazzola G, Di Rosolini MA, Larocca L, Bertino G, Digiacomo A, Benanti F, Guarneri L, Averna A, Iacobello C, Magro A, Scalisi I, Cartabellotta F, Savalli F, Barbara M, Davì A, Russello M, Scifo G, Squadrito G, Cammà C, Raimondo G, Craxì A, Di Marco V; Rete Sicilia Selezione Terapia–HCV (RESIST-HCV). Incidence of Hepatocellular Carcinoma in Patients With HCV-Associated Cirrhosis Treated With Direct-Acting Antiviral Agents. Gastroenterology 2018; 155: 411-421.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 153][Cited by in F6Publishing: 148][Article Influence: 51.0][Reference Citation Analysis (0)]
Yamada R, Hiramatsu N, Oze T, Urabe A, Tahata Y, Morishita N, Kodama T, Hikita H, Sakamori R, Yakushijin T, Yamada A, Hagiwara H, Mita E, Oshita M, Itoh T, Fukui H, Inui Y, Hijioka T, Inada M, Katayama K, Tamura S, Inoue A, Imai Y, Tatsumi T, Hamasaki T, Hayashi N, Takehara T. Incidence and risk factors of hepatocellular carcinoma change over time in patients with hepatitis C virus infection who achieved sustained virologic response.Hepatol Res. 2019;49:570-578.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 18][Cited by in F6Publishing: 16][Article Influence: 9.0][Reference Citation Analysis (0)]