The German trial on Aciclovir and Corticosteroids in Herpes-simplex-virus-Encephalitis (GACHE): a multicenter, randomized, double-blind, placebo-controlled trial.


Journal

Neurological research and practice
ISSN: 2524-3489
Titre abrégé: Neurol Res Pract
Pays: England
ID NLM: 101767802

Informations de publication

Date de publication:
2019
Historique:
received: 25 04 2019
accepted: 07 06 2019
entrez: 16 12 2020
pubmed: 12 9 2019
medline: 12 9 2019
Statut: epublish

Résumé

Comprehensive treatment of Herpes-simplex-virus-encephalitis (HSVE) remains a major clinical challenge. The current therapy gold standard is aciclovir, a drug that inhibits viral replication. Despite antiviral treatment, mortality remains around 20% and a majority of survivors suffer from severe disability. Experimental research and recent retrospective clinical observations suggest a favourable therapy response to adjuvant dexamethasone. Currently there is no randomized clinical trial evidence, however, to support the routine use of adjuvant corticosteroid treatment in HSVE. The German trial of Aciclovir and Corticosteroids in Herpes-simplex-virus-Encephalitis (GACHE) studied the effect of adjuvant dexamethasone versus placebo on top of standard aciclovir treatment in adult patients aged 18 up to 85 years with proven HSVE in German academic centers of Neurology in a randomized and double blind fashion. The trial was open from November 2007 to December 2012. The initially planned sample size was 372 patients with the option to increase to up to 450 patients after the second interim analysis. The primary endpoint was a binary functional outcome after 6 months assessed using the modified Rankin scale (mRS 0-2 vs. 3-6). Secondary endpoints included mortality after 6 and 12 months, functional outcome after 6 months measured with the Glasgow outcome scale (GOS), functional outcome after 12 months measured with mRS and GOS, quality of life as measured with the EuroQol 5D instrument after 6 and 12 months, neuropsychological testing after 6 months, cranial magnetic resonance imaging findings after 6 months, seizures up to day of discharge or at the latest at day 30, and after 6 and 12 months. The trial was stopped prematurely for slow recruitment after 41 patients had been randomized, 21 of them treated with dexamethasone and 20 with placebo. No difference was observed in the primary endpoint. In the full analysis set ( GACHE being prematurely terminated demonstrated challenges encountered performing randomized, placebo-controlled trials in rare life threatening neurological diseases. Based upon our trial results the use of adjuvant steroids in addition to antiviral treatment remains experimental and is at the decision of the individual treating physician. Unfortunately, the small number of study participants does not allow firm conclusions. EudraCT-Nr. 2005-003201-81.

Identifiants

pubmed: 33324892
doi: 10.1186/s42466-019-0031-3
pii: 31
pmc: PMC7650106
doi:

Types de publication

Journal Article

Langues

eng

Pagination

26

Informations de copyright

© The Author(s) 2019.

Déclaration de conflit d'intérêts

Competing interestsThe authors declare that they have no competing interests.

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Auteurs

U Meyding-Lamadé (U)

Department of Neurology, Krankenhaus Nordwest, Frankfurt, Germany.
Department of Neurology, University of Heidelberg, Heidelberg, Germany.

C Jacobi (C)

Department of Neurology, Krankenhaus Nordwest, Frankfurt, Germany.

F Martinez-Torres (F)

Department of Neurology, Krankenhaus Nordwest, Frankfurt, Germany.
Department of Neurology, University of Heidelberg, Heidelberg, Germany.

T Lenhard (T)

Department of Neurology, University of Heidelberg, Heidelberg, Germany.

B Kress (B)

Department of Neuroradiology, Krankenhaus Nordwest, Frankfurt, Germany.

M Kieser (M)

Department of Neurology, Charité Universitätsmedizin Berlin, Berlin, Germany.

C Klose (C)

Institute of Medical Biometry and Informatics, University of Heidelberg, Heidelberg, Germany.

K Einhäupl (K)

Department of Neurology, Charité Universitätsmedizin Berlin, Berlin, Germany.

J Bösel (J)

Department of Neurology, Klinikum Kassel, Kassel, Germany.

M-B Mackert (MB)

Department of Neurology, Vivantes Auguste-Viktoria-Klinikum, Berlin, Germany.

V Homberg (V)

Department of Neurology, Zentralklinik Bad Berka, Bad Berka, Germany.

C Koennecke (C)

Department of Neurology, Vivantes Klinikum im Friedrichshain, Berlin, Germany.

G Weißheit (G)

Department of Neurology, Vivantes Klinikum im Friedrichshain, Berlin, Germany.

D Claus (D)

Department of Neurology, Klinikum Darmstadt, Darmstadt, Germany.
Praxis Dr. Meyer & Prof. Claus, Bensheim, Germany.

B Kieseier (B)

Department of Neurology, Universitätsklinikum Frankfurt, Frankfurt, Germany.

J Bardutzky (J)

Department of Neurology, University of Freiburg, Freiburg, Germany.

T Neumann-Haefelin (T)

Department of Neurology, Klinikum Fulda, Fulda, Germany.

M W Lorenz (MW)

Department of Neurology, Krankenhaus Nordwest, Frankfurt, Germany.
Department of Neurology, Universitätsklinikum Frankfurt, Frankfurt, Germany.

H Steinmetz (H)

Department of Neurology, Universitätsklinikum Frankfurt, Frankfurt, Germany.

C Gerloff (C)

Department of Neurology, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.

D Schneider (D)

Department of Neurology, Universitätsklinikum Leipzig, Leipzig, Germany.

A Grau (A)

Department of Neurology, Klinikum der Stadt Ludwigshafen am Rhein, Lugwigshafen, Germany.

M Klein (M)

Department of Neurology, Klinikum der Ludwig-Maximilians- Universität München, Großhadern, Germany.

R Dziewas (R)

Department of Neurology, Universitätsklinikum Regensburg, Regensburg, Germany.

U Bogdahn (U)

Department of Pharmacy Heidelberg, Heidelberg University Hospital, Heidelberg, Germany.

W Jakob (W)

Department of Neurology, Universitätsklinikum Regensburg, Regensburg, Germany.

R Linker (R)

Department of Neurology, Universitätsklinikum Regensburg, Regensburg, Germany.

K Fuchs (K)

Department of Neurology, Universitätsklinikum Regensburg, Regensburg, Germany.

A Sander (A)

Institute of Medical Biometry and Informatics, University of Heidelberg, Heidelberg, Germany.

S Luntz (S)

Koordinierungszentrum für Klinische Studien (KKS), University of Heidelberg, Heidelberg, Germany.

T Hoppe-Tichy (T)

Department of Pharmacy Heidelberg, Heidelberg University Hospital, Heidelberg, Germany.

D F Hanley (DF)

Division of Brain Injury Outcomes, John Hopkins University, Baltimore, MD USA.

R von Kummer (R)

Universitätsklinikum Carl Gustav Carus, Dresden, Germany.

E Craemer (E)

Department of Neurology, Krankenhaus Nordwest, Frankfurt, Germany.

Classifications MeSH