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Published on 21 October 2010

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Higher success rate with zyvox

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of a new international phase 4 study of patients with nosocomial pneumonia due to culture-proven methicillin-resistant Staphylococcus aureus(MRSA) demonstrated that the antibiotic Zyvox (linezolid) achieved a statistically significantly higher clinical success rate compared with vancomycin for the primary endpoint. The ZEPHyR (Linezolid in the treatment of subjects with nosocomial pneumonia proven to be due to methicillin-resistant Staphylococcus aureus) study was the largest ever conducted in this population. These findings will be presented at the 48th Annual Meeting of the Infectious Diseases Society of America in Vancouver.

Investigators from 156 centres worldwide randomised 1,225 patients, of whom 448 patients had  proven MRSA nosocomial pneumonia (modified intent-to-treat group); 339 patients also met key protocol criteria at the end of study (per-protocol group) and were included in the primary analysis. Clinical success rates at the end of study were 57.6 percent (95/165) for patients treated with linezolid compared with 46.6 percent (81/174) for patients treated with vancomycin in the per-protocol group, the primary endpoint. These results demonstrated that linezolid achieved a statistically significantly higher clinical success rate compared to vancomycin (95 percent confidence interval for the difference in response rates: 0.5 percent, 21.6 percent; p=0.042). Results were consistent for the per-protocol group at end of treatment and for all MRSA pneumonia subjects (modified intent-to-treat) at end of treatment and end of study.  Microbiologic success was also consistent in both the per-protocol and the modified intent-to-treat groups at both end of treatment and end of study.

“Nosocomial pneumonia continues to be a significant cause of illness, and when these infections are due to MRSA, our options are limited, as there are few antibiotics that are effective against this resistant organism,” said study investigator Dr. Jean Chastre, Professor of Medicine and Critical Care Medicine, University Paris 6, Réanimation Médicale, Pitié-Salpêtrière Hospital, Paris.  “The findings, which show a higher cure rate for linezolid compared with vancomycin, provide important information for physicians who treat nosocomial pneumonia caused by MRSA.”

According to the European Centre for Disease Prevention and Control, an estimated 4.1 million patients acquire healthcare-associated infections (HCAI) in the EU every year and there are at least 37,000 deaths occurring as a direct consequence of these infections.1

The 2007 Annual Report of the European Antimicrobial Resistance Surveillance System (EARSS) describes the effectiveness of antibiotics across Europe between 1999 and 2006. The report found high prevalence of MRSA in most European Countries, with large intercountry and intercentre variations. The proportion of S. aureus infections due to MRSA varies from 0% in northern Europe to 50% in southern Europe, and rates of 60% have been reported in some intensive care units (ICU).2 Nosocomial pneumonia caused by resistant pathogens such as MRSA has the potential to become a severe and life-threatening infection. 3, 4

“Pfizer is committed to research in infectious diseases, and data from this large comparative study add to the body of evidence for linezolid in the treatment of MRSA nosocomial pneumonia and reinforce its efficacy in this patient population,” said Dr. Mark Kunkel, Executive Director, Clinical Group Lead for Anti-infective Drugs.

Safety data were assessed in all patients who received at least one dose of study drug, the intent-to-treat group (N=1,184).  Treatment-related adverse events, serious adverse events and deaths were comparable for linezolid and vancomycin.  Adverse events were considered treatment-related for 16.2 percent of linezolid patients and 18.4 percent of vancomycin subjects.  Treatment-related adverse events reported in 1 percent or more of linezolid patients were diarrhoea (3.7 percent), rash (2.7 percent), constipation (1.0 percent) and nausea (1.0 percent). Treatment-related adverse events reported in 1 percent or more of vancomycin patients were diarrhoea (4.3 percent), nausea (1.9 percent), rash (1.7 percent), anaemia (1.4 percent) and acute renal failure (1.4 percent).  Overall, 208  patients in each group reported serious adverse events; these were considered treatment-related in five linezolid patients and thirteen vancomycin patients.  Deaths occurred in 18.3 percent of patients who received linezolid and 19.4 percent of patients who received vancomycin.

Pfizer



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