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2.
Oncology ; 89 Suppl 2: 42-6, 2015.
Article in English | MEDLINE | ID: mdl-26584035

ABSTRACT

OBJECTIVES: The efficacy of the all-oral administration of daclatasvir and asunaprevir for 24 weeks was compared with that of telaprevir for 12 weeks plus pegylated interferon and ribavirin (PEG-IFN/RBV) for 24 weeks, and that of simeprevir for 12 weeks plus PEG-IFN/RBV for 24 weeks, with a focus on the prevention of occurrence and recurrence of hepatocellular carcinoma (HCC). The levels of alanine aminotransferase (ALT) and α-fetoprotein (AFP) as suppressive markers of HCC were also measured. METHODS: Patients received daclatasvir and asunaprevir (n = 17), simeprevir plus PEG-IFN/RBV (n = 15) and telaprevir plus PEG-IFN/RBV (n = 25). Sustained virological response (SVR) and the mean change in the level of serum ALT, AFP and platelet (PLT) count were compared among the three groups. RESULTS: No difference in SVR was observed in patients given daclatasvir with asunaprevir (SVR4), telaprevir plus PEG-IFN/RBV or simeprevir plus PEG-IFN/RBV (SVR24). Also, no significant difference was observed in the mean change of serum ALT, AFP or PLT count among the three groups. CONCLUSION: The preventive effect of the IFN-free, all-oral regimen of daclatasvir and asunaprevir was observed with a focus on the occurrence and recurrence of HCC, as was IFN-based treatment with telaprevir or simeprevir plus PEG-IFN/RBV.


Subject(s)
Antiviral Agents/therapeutic use , Carcinoma, Hepatocellular/prevention & control , Hepacivirus/drug effects , Hepatitis C, Chronic/drug therapy , Liver Neoplasms/prevention & control , Neoplasm Recurrence, Local/prevention & control , Adult , Aged , Aged, 80 and over , Carbamates , Carcinoma, Hepatocellular/epidemiology , Carcinoma, Hepatocellular/virology , Drug Therapy, Combination , Female , Follow-Up Studies , Genotype , Hepacivirus/genetics , Hepatitis C, Chronic/blood , Hepatitis C, Chronic/virology , Humans , Imidazoles/therapeutic use , Interferon alpha-2 , Interferon-alpha/therapeutic use , Isoquinolines/therapeutic use , Japan/epidemiology , Liver Neoplasms/epidemiology , Liver Neoplasms/virology , Male , Middle Aged , Neoplasm Recurrence, Local/epidemiology , Neoplasm Recurrence, Local/virology , Neoplasm Staging , Oligopeptides/therapeutic use , Polyethylene Glycols/therapeutic use , Polymerase Chain Reaction , Prognosis , Pyrrolidines , RNA, Viral/genetics , Recombinant Proteins/therapeutic use , Ribavirin/therapeutic use , Simeprevir/therapeutic use , Sulfonamides/therapeutic use , Valine/analogs & derivatives , Viral Load , alpha-Fetoproteins/analysis
3.
Oncology ; 89 Suppl 2: 60-9, 2015.
Article in English | MEDLINE | ID: mdl-26584037

ABSTRACT

At present, for adults with chronic hepatitis B virus (HBV) infection, two new analogues, entecavir (ETV) and tenofovir, are recommended as the first-line therapy by the EASL (European Association for the Study of the Liver), AASLD (American Association for the Study of Liver Diseases), and APASL (Asian Pacific Association for the Study of the Liver) guidelines. The use of pegylated interferon-α (PEG IFN-α) is recommended as the first-line therapy instead of standard IFN-α according to the above 3 guidelines. In this paper, the aim was to assess: (1) the long-term efficacy and safety as well as the resistance to ETV and tenofovir disoproxil fumarate (TDF); (2) the efficacy of PEG IFN-α; (3) the role of combination therapy with IFN plus two analogues, such as lamivudine and ETV; (4) the efficacy and safety of two analogues with cirrhosis, and (5) suppression of hepatocellular carcinoma (HCC) by ETV and IFN treatment. The results are as follows: (1) both ETV and TDF showed long-term efficacy and safety; (2) PEG IFN-α resulted in a greater decline in HBV DNA levels and a higher rate of HBeAg seroconversion; (3) combination therapy with IFN plus two analogues did not elevate the rate of sustained responses; (4) both ETV and TDF showed efficacy and safety with cirrhosis (ETV especially displayed efficacy and safety with decompensated cirrhosis), and (5) suppression of HCC was observed by ETV and IFN.


Subject(s)
Antiviral Agents/therapeutic use , Carcinoma, Hepatocellular/prevention & control , Hepacivirus/drug effects , Hepatitis C, Chronic/drug therapy , Liver Neoplasms/prevention & control , Practice Guidelines as Topic , Adult , Carcinoma, Hepatocellular/epidemiology , Carcinoma, Hepatocellular/virology , Clinical Trials as Topic , Disease Management , Drug Therapy, Combination , Guanine/analogs & derivatives , Guanine/therapeutic use , Hepacivirus/genetics , Hepatitis C, Chronic/blood , Hepatitis C, Chronic/virology , Humans , Interferon-alpha/therapeutic use , Japan/epidemiology , Liver Neoplasms/epidemiology , Liver Neoplasms/virology , Prognosis
4.
Dig Dis ; 33(6): 715-20, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26488474

ABSTRACT

OBJECTIVE: The aim of this study was to evaluate cytokeratin-18M65 (CK-18M65) for distinguishing between simple steatosis (SS) and non-alcoholic steatohepatitis (NASH) against healthy individuals (HIs) in Japanese population. METHODS: The serum from 24 HIs, 21 patients with SS and 20 patients with NASH were examined. Serum CK-18M65 was measured by enzyme-linked immunosorbent assay. RESULTS: Aspartate aminotransferase was significantly different between NASH patients and HIs with p < 0.0001 (SS patients and HIs: p < 0.0001), as was alanine aminotransferase between NASH patients and HIs with p < 0.0001 (SS patients and HIs: p < 0.0001). Serum CK-18M65 increased in a stepwise fashion in HIs and also in SS and NASH patients. Multivariate logistic regression analysis revealed that NASH could be diagnosed with the use of CK-18M65 alone (p = 0.0285, OR 1.0038, 95% CI 1.0004-1.0073). At the optimal cut-off level of 548 U/l, CK-18M65 had an AUC value of 0.7369, 60.00% sensitivity and 85.70% specificity. In patients with NASH, no significant difference was observed between low fibrosis (Stage 0-1, 794.30 ± 454.41, n = 10) and high fibrosis (Stage 2-3, 809.70 ± 641.43, n = 10; p = 0.5967) and between slight steatosis (<33%, 512.89 ± 229.65, n = 9) and moderate steatosis (≥33%, 655.13 ± 480.78, n = 32) in patients with non-alcoholic fatty liver disease (NAFLD; p = 0.7647) with the use of CK-18M65. CONCLUSION: Serum CK-18M65 distinguished NASH from SS, but could not assess the severity of steatosis in NAFLD patients or the grade of fibrosis in NASH patients in Japanese population.


Subject(s)
Keratin-18/blood , Non-alcoholic Fatty Liver Disease/diagnosis , Adult , Aged , Asian People , Biomarkers/blood , Diagnosis, Differential , Enzyme-Linked Immunosorbent Assay , Fatty Liver/blood , Fatty Liver/diagnosis , Female , Humans , Male , Middle Aged , Non-alcoholic Fatty Liver Disease/blood
5.
Dig Dis ; 33(6): 721-7, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26488580

ABSTRACT

OBJECTIVES: The characteristics of hypovascular and hypervascular well-differentiated hepatocellular carcinomas (HCCs) were compared in terms of tumor size, tumor markers and detectability by imaging modalities. METHODS: Well-differentiated HCC nodules that are smaller than 2 cm (n = 27) were evaluated in 27 patients using histopathology and divided into 2 groups: hypovascular (n = 10) and hypervascular (n = 17). The diagnostic sensitivity of imaging modalities was then evaluated for efficiency in disclosing tumor size and tumor markers in the 2 types. RESULTS: No difference was observed in tumor size and tumor markers between the 2 types; however, the sensitivity of contrast-enhanced CT, contrast-enhanced ultrasonography and arterioportal angiography was significantly different between the 2 types, whereas that by Gadolinium-ethoxybenzyl-diethylenetriamine pentaacetic acid enhanced magnetic resonance imaging (Gd-EOB-DTPA MRI) demonstrated no difference. CONCLUSION: Hypovascular HCC could be diagnosed by Gd-EOB-DTPA MRI in the hepatobiliary phase.


Subject(s)
Biomarkers, Tumor/blood , Carcinoma, Hepatocellular/blood supply , Carcinoma, Hepatocellular/diagnosis , Liver Neoplasms/blood supply , Liver Neoplasms/diagnosis , Aged , Aged, 80 and over , Angiography , Biomarkers/blood , Carcinoma, Hepatocellular/blood , Carcinoma, Hepatocellular/pathology , Contrast Media , Female , Gadolinium DTPA , Humans , Image Enhancement , Liver/blood supply , Liver/pathology , Liver Neoplasms/blood , Liver Neoplasms/pathology , Magnetic Resonance Imaging , Male , Middle Aged , Neoplasm Staging , Protein Precursors/blood , Prothrombin , Sensitivity and Specificity , Tomography, X-Ray Computed , Ultrasonography , alpha-Fetoproteins/analysis
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