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Douhara et al. Hepatoma Res 2017;3:215-20                            Hepatoma Research
           DOI: 10.20517/2394-5079.2017.32
                                                                                                  www.hrjournal.net
            Original Article                                                                    Open Access

           Efficacy and HCC development after DAA

           therapy for patients with chronic hepatitis C:

           a single center retrospective cohort study



           Akitoshi Douhara, Hiroyuki Ogawa, Satoshi Nakatani, Takahiro Ozutsumi, Erika Shioyama, Masaaki Yoshikawa,
           Shigehiko Ueda
           Internal Medicine, Kokuho Central Hospital 404-1, Miyako, Tawaramoto-cho, Shiki-gun, Nara Prefecture 636-0302, Japan.

           Correspondence to: Dr. Akitoshi Douhara, Internal Medicine, Kokuho Central Hospital 404-1, Miyako, Tawaramoto-cho, Shiki-gun, Nara Prefecture
           636-0302, Japan. E-mail: aki-do@hotmail.co.jp

           How to cite this article: Douhara A, Ogawa H, Nakatani S, Ozutsumi T, Shioyama E, Yoshikawa M, Ueda S. Efficacy and HCC development after
           DAA therapy for patients with chronic hepatitis C: a single center retrospective cohort study. Hepatoma Res 2017;3:215-20.
                                         ABSTRACT

            Article history:              Aim: The development of hepatocellular carcinoma (HCC) is reduced after interferon based
            Received: 28 Jul 2017         treatment in patients with chronic hepatitis C (CHC). A new therapy using direct-acting
            Accepted: 20 Sep 2017         antiviral agents (DAA) has been widely applied since 2014 for CHC. The purpose of this
            Published: 17 Oct 2017        study is to investigate the efficacy, safety and development of HCC after DAA treatment.
                                          Methods: The authors enrolled 33 consecutive patients who were treated with DAA for CHC
            Key words:                    at the hospital between January 2015 and March 2016. The laboratory data were collected
            Chronic hepatitis C,          at  the  start  and  24  weeks  after  DAA  therapy.  Results:  The  authors  analyzed  33  patients
            direct-acting antiviral therapy,  (18 male, 15 female, mean age of 68-year-old). The hepatic C virus genotypes were type 1
            development of hepatocellular   (27 patients) and type 2 (6 patients). The number of patients treated with sofosbuvir (SOF) +
            carcinoma,                    ledipasvir, daclatasvir + asunaprevir and SOF + ribavirin was 14, 13 and 6, respectively. The
            sarcoidosis                   sustained virological response (SVR24) rate was 100%. Aspartate aminotransferase, alanine
                                          aminotransferase and FIB4-index were significantly decreased after SVR24. Adverse effects
                                          were observed in 9 patients (anemia, 5; liver function test disorder, 2; sarcoidosis, 1; pruritus, 1).
                                          With regard to HCC development, one elderly patient (3.0%) had multiple HCC recurrence
                                          after SVR24. Conclusion: DAA therapy achieved a high SVR24 rate with a good serological
                                          response. However, one patient had multiple HCC recurrence. These findings indicate that
                                          careful follow-up may be essential after DAA therapy.


           INTRODUCTION                                       (DAA) for patients with chronic CHC directly target
                                                              HCV replication and have been widely used globally
           During the previous decades, Pegylated interferon   since 2014. Compared to conventional IFN-therapy,
           (PEG-IFN) plus ribavirin therapy for patients with chronic   the sustained virological response (SVR) rate is higher
           hepatitis C (CHC) cured hepatic C virus (HCV) infection   and the side effects are reduced with DAA therapy.
           in approximately 50% of treated patients . Emerging   Previously,  it  was  reported  that  IFN-based  therapy
                                                [1]
           treatments with IFN-free direct-acting antiviral agents   reduced the risk of liver complications,  including the

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