Treatment of chronic hepatitis C genotype 1 patients at an academic center in Europe involved in prospective, controlled trials

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Treatment of chronic hepatitis C genotype 1 patients at an academic center in Europe involved in prospective, controlled trials : is there a selection bias? / Beinhardt, Sandra; Staettermayer, Albert F; Rutter, Karoline; Maresch, Judith; Scherzer, Thomas M; Steindl-Munda, Petra; Hofer, Harald; Ferenci, Peter.

in: HEPATOLOGY, Jahrgang 55, Nr. 1, 01.01.2012, S. 30-8.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Beinhardt, S, Staettermayer, AF, Rutter, K, Maresch, J, Scherzer, TM, Steindl-Munda, P, Hofer, H & Ferenci, P 2012, 'Treatment of chronic hepatitis C genotype 1 patients at an academic center in Europe involved in prospective, controlled trials: is there a selection bias?', HEPATOLOGY, Jg. 55, Nr. 1, S. 30-8. https://doi.org/10.1002/hep.24671

APA

Beinhardt, S., Staettermayer, A. F., Rutter, K., Maresch, J., Scherzer, T. M., Steindl-Munda, P., Hofer, H., & Ferenci, P. (2012). Treatment of chronic hepatitis C genotype 1 patients at an academic center in Europe involved in prospective, controlled trials: is there a selection bias? HEPATOLOGY, 55(1), 30-8. https://doi.org/10.1002/hep.24671

Vancouver

Bibtex

@article{4d09f0e43b094a15b135e73a0d5cb990,
title = "Treatment of chronic hepatitis C genotype 1 patients at an academic center in Europe involved in prospective, controlled trials: is there a selection bias?",
abstract = "UNLABELLED: Pegylated interferon-alpha2/ribavirin (peg-IFN/RBV) is the standard of care (SOC) for patients with chronic hepatitis C (CHC) infection. Currently, direct-acting antiviral agents (DAAs) are evaluated in clinical trials. The aim of this study was to compare baseline characteristics and sustained virologic response (SVR) rates in patients included in clinical trials to those receiving SOC. Medical records of all 503 treatment-na{\"i}ve patients with CHC, genotype (GT) 1, referred over a 4-year period (January 2006-December 2009) were reviewed. Only 310 of 503 (62%) patients received antiviral therapy, 141 were enrolled in randomized, controlled trials ({"}study patients{"}; 101 in DAA studies), and 169 received SOC. At baseline, viral load and platelet count were higher and bilirubin was lower in study patients than in SOC patients. History of psychiatric disorders was more common in SOC patients (43 [25%] versus study patients with 18 [13%]; P < 0.01). Liver biopsy was obtained in 98% of study patients, but only in 59% of SOC patients. Twenty-nine (21%) and 40 (40%) study and SOC patients, respectively, had advanced fibrosis (F3/4; P = 0.001). By intent-to-treat analysis, SVR rates were higher in DAAs (64%; 95% confidence interval [CI]: 53.4-74.4) than in SOC patients (46%; 95% CI: 37.9-53.7; P < 0.01), but not different when calculated on a treated-per-protocol (TPP) basis. Interleukin (IL)28B GT was equally distributed in both cohorts. By chance, more patients treated with IFN/RBV had rs12979860 C/C-GT (up to 44%) than DAA-treated patients. If analyzed according to the IL28B polymorphism, TPP SVR rates did not reach statistically significant differences among study and SOC patients.CONCLUSIONS: Baseline characteristics slightly favored study patients, but IL28B GT and treatment adherence were the most important factors determining outcome. Thus, the applicability of the results of controlled studies has to be tested in a {"}real-world{"} setting.",
keywords = "Academic Medical Centers, Adult, Antiviral Agents, Europe, Female, Genotype, Hepacivirus, Hepatitis C, Chronic, Humans, Interleukins, Male, Middle Aged, Patient Selection, Polymorphism, Genetic, Prospective Studies, Randomized Controlled Trials as Topic, Retrospective Studies, Selection Bias, Treatment Outcome",
author = "Sandra Beinhardt and Staettermayer, {Albert F} and Karoline Rutter and Judith Maresch and Scherzer, {Thomas M} and Petra Steindl-Munda and Harald Hofer and Peter Ferenci",
note = "Copyright {\textcopyright} 2011 American Association for the Study of Liver Diseases.",
year = "2012",
month = jan,
day = "1",
doi = "10.1002/hep.24671",
language = "English",
volume = "55",
pages = "30--8",
journal = "HEPATOLOGY",
issn = "0270-9139",
publisher = "John Wiley and Sons Ltd",
number = "1",

}

RIS

TY - JOUR

T1 - Treatment of chronic hepatitis C genotype 1 patients at an academic center in Europe involved in prospective, controlled trials

T2 - is there a selection bias?

AU - Beinhardt, Sandra

AU - Staettermayer, Albert F

AU - Rutter, Karoline

AU - Maresch, Judith

AU - Scherzer, Thomas M

AU - Steindl-Munda, Petra

AU - Hofer, Harald

AU - Ferenci, Peter

N1 - Copyright © 2011 American Association for the Study of Liver Diseases.

PY - 2012/1/1

Y1 - 2012/1/1

N2 - UNLABELLED: Pegylated interferon-alpha2/ribavirin (peg-IFN/RBV) is the standard of care (SOC) for patients with chronic hepatitis C (CHC) infection. Currently, direct-acting antiviral agents (DAAs) are evaluated in clinical trials. The aim of this study was to compare baseline characteristics and sustained virologic response (SVR) rates in patients included in clinical trials to those receiving SOC. Medical records of all 503 treatment-naïve patients with CHC, genotype (GT) 1, referred over a 4-year period (January 2006-December 2009) were reviewed. Only 310 of 503 (62%) patients received antiviral therapy, 141 were enrolled in randomized, controlled trials ("study patients"; 101 in DAA studies), and 169 received SOC. At baseline, viral load and platelet count were higher and bilirubin was lower in study patients than in SOC patients. History of psychiatric disorders was more common in SOC patients (43 [25%] versus study patients with 18 [13%]; P < 0.01). Liver biopsy was obtained in 98% of study patients, but only in 59% of SOC patients. Twenty-nine (21%) and 40 (40%) study and SOC patients, respectively, had advanced fibrosis (F3/4; P = 0.001). By intent-to-treat analysis, SVR rates were higher in DAAs (64%; 95% confidence interval [CI]: 53.4-74.4) than in SOC patients (46%; 95% CI: 37.9-53.7; P < 0.01), but not different when calculated on a treated-per-protocol (TPP) basis. Interleukin (IL)28B GT was equally distributed in both cohorts. By chance, more patients treated with IFN/RBV had rs12979860 C/C-GT (up to 44%) than DAA-treated patients. If analyzed according to the IL28B polymorphism, TPP SVR rates did not reach statistically significant differences among study and SOC patients.CONCLUSIONS: Baseline characteristics slightly favored study patients, but IL28B GT and treatment adherence were the most important factors determining outcome. Thus, the applicability of the results of controlled studies has to be tested in a "real-world" setting.

AB - UNLABELLED: Pegylated interferon-alpha2/ribavirin (peg-IFN/RBV) is the standard of care (SOC) for patients with chronic hepatitis C (CHC) infection. Currently, direct-acting antiviral agents (DAAs) are evaluated in clinical trials. The aim of this study was to compare baseline characteristics and sustained virologic response (SVR) rates in patients included in clinical trials to those receiving SOC. Medical records of all 503 treatment-naïve patients with CHC, genotype (GT) 1, referred over a 4-year period (January 2006-December 2009) were reviewed. Only 310 of 503 (62%) patients received antiviral therapy, 141 were enrolled in randomized, controlled trials ("study patients"; 101 in DAA studies), and 169 received SOC. At baseline, viral load and platelet count were higher and bilirubin was lower in study patients than in SOC patients. History of psychiatric disorders was more common in SOC patients (43 [25%] versus study patients with 18 [13%]; P < 0.01). Liver biopsy was obtained in 98% of study patients, but only in 59% of SOC patients. Twenty-nine (21%) and 40 (40%) study and SOC patients, respectively, had advanced fibrosis (F3/4; P = 0.001). By intent-to-treat analysis, SVR rates were higher in DAAs (64%; 95% confidence interval [CI]: 53.4-74.4) than in SOC patients (46%; 95% CI: 37.9-53.7; P < 0.01), but not different when calculated on a treated-per-protocol (TPP) basis. Interleukin (IL)28B GT was equally distributed in both cohorts. By chance, more patients treated with IFN/RBV had rs12979860 C/C-GT (up to 44%) than DAA-treated patients. If analyzed according to the IL28B polymorphism, TPP SVR rates did not reach statistically significant differences among study and SOC patients.CONCLUSIONS: Baseline characteristics slightly favored study patients, but IL28B GT and treatment adherence were the most important factors determining outcome. Thus, the applicability of the results of controlled studies has to be tested in a "real-world" setting.

KW - Academic Medical Centers

KW - Adult

KW - Antiviral Agents

KW - Europe

KW - Female

KW - Genotype

KW - Hepacivirus

KW - Hepatitis C, Chronic

KW - Humans

KW - Interleukins

KW - Male

KW - Middle Aged

KW - Patient Selection

KW - Polymorphism, Genetic

KW - Prospective Studies

KW - Randomized Controlled Trials as Topic

KW - Retrospective Studies

KW - Selection Bias

KW - Treatment Outcome

U2 - 10.1002/hep.24671

DO - 10.1002/hep.24671

M3 - SCORING: Journal article

C2 - 21932410

VL - 55

SP - 30

EP - 38

JO - HEPATOLOGY

JF - HEPATOLOGY

SN - 0270-9139

IS - 1

ER -