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PLoS Medicine 7, 11 (2010) e1000362
Efficacy of oseltamivir-zanamivir combination compared to each monotherapy for seasonal influenza: a randomized placebo-controlled trial.
Xavier Duval 1, 2, Sylvie Van Der Werf 3, 4, Thierry Blanchon 5, Anne Mosnier 6, Maude Bouscambert-Duchamp 7, 8, Annick Tibi 9, Vincent Enouf 3, Cécile Charlois-Ou 10, Corine Vincent 1, 11, Laurent Andreoletti 12, 13, Florence Tubach 1, 11, Bruno Lina 7, 8, France Mentré 1, 11, Catherine Leport ( ) 10, 14
Bivir Study Group Collaboration(s)
(2010)

BACKGROUND: Neuraminidase inhibitors are thought to be efficacious in reducing the time to alleviation of symptoms in outpatients with seasonal influenza. The objective of this study was to compare the short-term virological efficacy of oseltamivir-zanamivir combination versus each monotherapy plus placebo. METHODS AND FINDINGS: We conducted a randomized placebo-controlled trial with 145 general practitioners throughout France during the 2008-2009 seasonal influenza epidemic. Patients, general practitioners, and outcome assessors were all blinded to treatment assignment. Adult outpatients presenting influenza-like illness for less than 36 hours and a positive influenza A rapid test diagnosis were randomized to oseltamivir 75 mg orally twice daily plus zanamivir 10 mg by inhalation twice daily (OZ), oseltamivir plus inhaled placebo (O), or zanamivir plus oral placebo (Z). Treatment efficacy was assessed virologically according to the proportion of patients with nasal influenza reverse transcription (RT)-PCR below 200 copies genome equivalent (cgeq)/µl at day 2 (primary outcome), and clinically to the time to alleviation of symptoms until day 14. Overall 541 patients (of the 900 planned) were included (OZ, =192; O, n=176; Z, n=173), 49% male, mean age 39 years. In the intention-to-treat analysis conducted in the 447 patients with RT-PCR-confirmed influenza A, 46%, 59%, and 34% in OZ (n=157), O (n=141), and Z (n=149) arms had RT-PCR<200 cgeq/µl (-13.0%, 95% confidence interval [CI] -23.1 to -2.9, p=0.025; +12.3%, 95% CI 2.39-22.2, p=0.028 for OZ/O and OZ/Z comparisons). Mean day 0 to day 2 viral load decrease was 2.14, 2.49, and 1.68 log(10) cgeq/µl (p=0.060, p=0.016 for OZ/O and OZ/Z). Median time to alleviation of symptoms was 4.0, 3.0, and 4.0 days (+1.0, 95% CI 0.0-4.0, p=0.018; +0.0, 95% CI -3.0 to 3.0, p=0.960 for OZ/O and OZ/Z). Four severe adverse events were observed. Nausea and/or vomiting tended to be more frequent in the combination arm (OZ, n=13; O, n=4; and Z, n=5 patients, respectively). CONCLUSIONS: In adults with seasonal influenza A mainly H3N2 virus infection, the oseltamivir-zanamivir combination appeared less effective than oseltamivir monotherapy, and not significantly more effective than zanamivir monotherapy. Despite the theoretical potential for the reduction of the emergence of antiviral resistance, the lower effectiveness of this combination calls for caution in its use in clinical practice. TRIAL REGISTRATION: www.ClinicalTrials.govNCT00799760.
1 :  Modèles et méthodes de l'évaluation thérapeutique des maladies chroniques
INSERM : U738 – Université Paris VII - Paris Diderot
2 :  CIC - CHU Bichat
INSERM : CIC7
3 :  Génétique moléculaire des virus à ARN
Institut Pasteur de Paris – CNRS : URA3015
4 :  Centre National de Référence du virus influenzae, région Nord-Génétique Moléculaire des Virus à ARN (CNR)
Institut Pasteur de Paris
5 :  Epidémiologie des maladies infectieuses et modélisation (ESIM)
INSERM : U707 – Université Pierre et Marie Curie [UPMC] - Paris VI
6 :  Réseau des Groupes Régionaux d'Observation de la Grippe (GROG)
Coordination nationale
7 :  Virologie et Pathologie Humaine (VirPath)
CNRS : FRE3011 – Université Claude Bernard - Lyon I – École Normale Supérieure - Lyon
8 :  Centre National de Référence Virus Influenza (Région Sud)
Hospices Civils de Lyon
9 :  Agence Générale des Equipements et Produits de Santé
Assistance publique - Hôpitaux de Paris (AP-HP)
10 :  Laboratoire de Recherche en Pathologie Infectieuse
Université Paris VII - Paris Diderot
11 :  Département d'épidémiologie, biostatistique et recherche clinique
Assistance publique - Hôpitaux de Paris (AP-HP) – Hôpital Bichat - Claude Bernard
12 :  Inflammation et immunité de l'épithélium respiratoire
IFR53 – Université de Reims - Champagne Ardenne : EA4303
13 :  Unité de virologie médicale [Reims]
Hôpital Robert Debré
14 :  Unité de Coordination des Risques Epidémiques et Biologiques
Assistance publique - Hôpitaux de Paris (AP-HP)
Sciences du Vivant/Médecine humaine et pathologie/Maladies infectieuses
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