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Efficacy and safety of long-term therapy with nucleos(t)ide analogues in chronic hepatitis B

Ибрагимов Э. К., Абдурахманов Д. Т., Розина Т. П., Никулкина Е. Н., Танасчук Е. Л., Одинцов А. В., Паневкина С. В., Моисеев С. В.
Терапевтический архив
Т. 91, Вып. 2, С. 40-47
Опубликовано: 2019
Тип ресурса: Статья

DOI:10.26442/00403660.2019.02.000073

Аннотация:
Nucleos(t)ide analogues are first-line therapies for the treatment of chronic hepatitis B. However, the efficacy and safety of long-term treatment and the necessary duration of therapy remains the subject of discussion. Aim. To assess the efficacy and safety of long-term treatment with nucleos(t)ide analogues in patients with chronic hepatitis B. Materials and methods. We conducted an observational study in 101 chronic hepatitis B (HBeAg-negative and HBeAg-positive) patients treated (≥3 years) with entecavir, tenofovir or telbivudine. Results and discussion. Treatment with entecavir and tenofovir was associated with high rate of virologic and biochemical response (>95[%]) and HBeAg seroconversion (93[%] and 67[%], respectively). Cumulative rate of virologic resistance was 0; 3.1[%] and 43.5[%] for tenofovir, entecavir and telbivudine, respectively. Long-term nucleos(t)ide analogues treatment resulted in a regress of liver fibrosis (from 8.92 to 7.18 kPa, ð<0.0001) and reduction in the number of
Ключевые слова:
ALT normalization; Chronic hepatitis B; HBeAg seroconversion; HBsAg clearance; Nucleos(t)ide analogues; Safety; Virologic response
antivirus agent; entecavir; guanine; hepatitis B(e) antigen; nucleic acid synthesis inhibitor; telbivudine; tenofovir; analogs and derivatives; chronic hepatitis B; Hepatitis B virus; human; time factor; treatment outcome; Antiviral Agents; Guanine; Hepatitis B e Antigens; Hepatitis B virus; Hepatitis B, Chronic; Humans; Nucleic Acid Synthesis Inhibitors; Telbivudine; Tenofovir; Time Factors; Treatment Outcome
Язык текста: Русский
ISSN: 2309-5342
Ибрагимов Э. К. Эльхан Кямранович 1989-
Абдурахманов Д. Т. Джамал Тинович 1967-
Розина Т. П. Тэона Павловна 1974-
Никулкина Е. Н.
Танасчук Е. Л.
Одинцов А. В. Алексей Владимирович 1964-
Паневкина С. В.
Моисеев С. В. Сергей Валентинович 1960-
Ibragimov E`. K. E`l`khan Kyamranovich 1989-
Abdurakhmanov D. T. Dzhamal Tinovich 1967-
Rozina T. P. Te`ona Pavlovna 1974-
Nikulkina E. N.
Tanaschuk E. L.
Odintsov A. V. Aleksej Vladimirovich 1964-
Panevkina S. V.
Moiseev S. V. Sergej Valentinovich 1960-
Efficacy and safety of long-term therapy with nucleos(t)ide analogues in chronic hepatitis B
Текст визуальный непосредственный
Терапевтический архив
Медицинское маркетинговое агентство "МедиаМедика"
Т. 91, Вып. 2 С. 40-47
2019
Статья
ALT normalization Chronic hepatitis B HBeAg seroconversion HBsAg clearance Nucleos(t)ide analogues Safety Virologic response
antivirus agent entecavir guanine hepatitis B(e) antigen nucleic acid synthesis inhibitor telbivudine tenofovir analogs and derivatives chronic hepatitis B Hepatitis B virus human time factor treatment outcome Antiviral Agents Guanine Hepatitis B e Antigens Hepatitis B virus Hepatitis B, Chronic Humans Nucleic Acid Synthesis Inhibitors Telbivudine Tenofovir Time Factors Treatment Outcome
Nucleos(t)ide analogues are first-line therapies for the treatment of chronic hepatitis B. However, the efficacy and safety of long-term treatment and the necessary duration of therapy remains the subject of discussion. Aim. To assess the efficacy and safety of long-term treatment with nucleos(t)ide analogues in patients with chronic hepatitis B. Materials and methods. We conducted an observational study in 101 chronic hepatitis B (HBeAg-negative and HBeAg-positive) patients treated (≥3 years) with entecavir, tenofovir or telbivudine. Results and discussion. Treatment with entecavir and tenofovir was associated with high rate of virologic and biochemical response (>95[%]) and HBeAg seroconversion (93[%] and 67[%], respectively). Cumulative rate of virologic resistance was 0; 3.1[%] and 43.5[%] for tenofovir, entecavir and telbivudine, respectively. Long-term nucleos(t)ide analogues treatment resulted in a regress of liver fibrosis (from 8.92 to 7.18 kPa, ð<0.0001) and reduction in the number of