Evolution of HCV patient characteristics and DAA regimens in the German Hepatitis C Registry (DHC-R) in 2014 and 2015

被引:2
作者
Sarrazin, Christoph [1 ]
Buggisch, Peter [2 ]
Mauss, Stefan [3 ]
Mueller, Tobias [4 ]
Zimmermann, Tim [5 ]
Klinker, Hartwig [6 ]
Pathil-Warth, Anita [7 ]
Schlag, Michael [8 ]
Nalpas, Catherine [9 ]
Wegner, Sven [10 ]
Lonjon-Domanec, Isabelle [11 ]
Simon, Karl-Georg
机构
[1] St Josefs Hosp Wiesbaden, Med Klin 2, Beethovenstr 20, D-65189 Wiesbaden, Germany
[2] Ifi Inst Interdisciplinary Med, Hamburg, Germany
[3] Ctr HIV & Hepatogastroenterol, Dusseldorf, Germany
[4] Charite Campus Virchow Klinikum CVK, Dept Internal Med Hepatol & Gastroenterol, Berlin, Germany
[5] Johannes Gutenberg Univ Mainz, Gastroenterol & Hepatol, Med Klin & Poliklin 1, Mainz, Germany
[6] Univ Hosp Wurzburg, Div Infect Dis, Dept Internal Med 2, Wurzburg, Germany
[7] Univ Klinikum Heidelberg, Dept Internal Med Gastroenterol 4, Heidelberg, Germany
[8] Janssen Cilag Pharma GmbH, EMEA Med Affairs, Vienna, Austria
[9] Janssen Pharmaceut, EMEA Med Affairs, Paris, France
[10] Janssen Cilag GmbH, Fachbereich Infektiol, Neuss, Germany
[11] Janssen Cilag, EMEA Med Affairs, Paris, France
来源
ZEITSCHRIFT FUR GASTROENTEROLOGIE | 2019年 / 57卷 / 05期
关键词
hepatitis C; simeprevir; DAA; SVR; Germany; cirrhosis; SUSTAINED VIROLOGICAL RESPONSE; ACTING ANTIVIRAL THERAPY; GENOTYPE; VIRUS-INFECTION; TREAT PATIENTS; SOFOSBUVIR; RIBAVIRIN; CIRRHOSIS;
D O I
10.1055/a-0859-7561
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background The urgent need in HCV-infected patients with liver disease mandated the rapid implementation of IFN-free DAA combination therapies following their regulatory approval in 2014 and 2015 without full knowledge of the optimal combinations and regimens. Investigating the evolution of the DAA utilization patterns and treatment outcomes could provide learnings for future situations. Methods This was an analysis of a prospective observational database from the German Hepatitis C Registry (DHC-R) covering a period from May 2014 to September 2015. Adult patients had evidence of chronic HCV GT1 or GT4 infection and were treated with an IFN-free combination regimen of simeprevir (SMV) + sofosbuvir (SOF) or other IFN-free regimens: daclatasvir + sofosbuvir (DCV + SOF), ledipasvir/sofosbuvir (SOF/LDV), paritaprevir/r + ombitasvir dasabuvir (PrOD), with or without ribavirine (R). Results A total of 5496 subjects were followed during the period. During this period, clinical recommendations and treatment patterns evolved rapidly in response to new evidence from clinical trials and clinical routine and regulatory approval of additional regimens. High SVR12 rates were seen in this cohort, even in hard-to-treat patient subgroups. In the multivariate analysis, gender, age, advanced cirrhosis, and intensified treatment for cirrhotics were associated with treatment outcome. Conclusion Despite limited knowledge of the optimal utilization of the newly approved DAA combinations and treatment durations as well as their comparative efficacy and safety profiles, high SVR rates were achieved regardless of the DAA combination. These outcomes were facilitated by the rapid adaptation of clinical recommendations. Future situations with high unmet medical need may follow a similar approach.
引用
收藏
页码:584 / 592
页数:9
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