Developments, news and strategies for drug development specific to phase I through Phase III global clinical trial management, execution, project management and outsourcing. Go→
News, articles and issues specific to clinical trial practice and implementation at the investigative site level. Go→
News, developments and strategies related to eClinical, data management, data collection, ePRO, and more information technology used in the drug development chain. Go→
News, articles and issues specific to laboratories role in the clinical trial, including ECG, imaging, genotyping, tissue samples and more. Go→
News, developments and strategies for clinical trials conduct in relation to the FDA, EMEA and other global regulatory authorities overseeing the drug development industry. Go→
News, articles and strategies related to clinical trial design which impact postmarketing studies, therapeutic areas, adaptive trials, statistics, protocols and more. Go→
|
|
Real-world study comparing commonly prescribed COPD medicines shows choice of treatment has impact on patient outcomes
Publish date: Mar 22, 2013
![]()
Canada NewsWire MISSISSAUGA, ON, March 22, 2013
MISSISSAUGA, ON, March 22, 2013 /CNW/ - PATHOS
is the largest real-world study to compare the effectiveness of two
commonly prescribed inhaled corticosteroid and long-acting beta agonist
(ICS/LABA) combination treatments for chronic obstructive pulmonary
disease (COPD) with more than one year of patient follow-up.1 An analysis of PATHOS data shows that COPD patients
treated with
SYMBICORT® (budesonide/formoterol) are significantly less likely to suffer from COPD-related exacerbations
- or 'flare ups' - and are significantly less likely to be hospitalized
for COPD than those treated with ADVAIR® (fluticasone/salmeterol).1
Overall, SYMBICORT® reduced the annual rate of moderate to severe exacerbations by 26 per
cent compared to ADVAIR® (0.80 vs. 1.09 /patient-year; p<0.0001).1 The significant and clinically
relevant reduction in favour of
SYMBICORT® was apparent for all types of exacerbation events (e.g. antibiotic use,
oral steroid use or hospital admission).1 Indeed, use of SYMBICORT® reduced rates of COPD-related
hospitalization by 29 per cent (0.15 vs.
0.21 /patient-year; p<0.0001) with hospital days due to COPD
exacerbation 34 per cent fewer (0.63 vs. 0.95/patient-year; p<0.0001)
compared with ADVAIR®.1 This analysis of the PATHOS
data was recently published in the Journal of Internal Medicine.1
"COPD is rapidly becoming one of the world's most serious health issues
and is the fourth leading cause of death in Canada," said Dr. Charlie
Chan
, Professor and Vice-Chair of Medicine, University of Toronto, consultant
Respirologist, University Health Network. "As a real-world evidence study, PATHOS plays an important role in
helping healthcare professionals understand the impact of COPD
treatment options on patient outcomes, and coupled with rigorous
clinical trial data analysis, can provide a more fulsome picture of
disease patterns patients are experiencing."
The 11-year PATHOS study, led by Uppsala University, retrospectively
examined the medical records of 5,468* ICS/LABA-treated patients in
Sweden from 1999 to 2009; comprising a total of 19,000 patient years.1 This first
published analysis of the data compares the rate of COPD
exacerbations associated with two commonly prescribed combinations.1 To allow for a valid comparison, a cohort
of patients treated with
SYMBICORT® were individually matched with an equal number of patients treated with
a second ICS/LABA, ADVAIR®.1 Investigators used a statistical technique called "propensity score
matching" to minimize bias and ensure the two ICS/LABA-treated groups
were comparable in terms of variables including age, gender and
measures of disease severity such as medication use, COPD
co-morbidities, previous hospitalizations for any cause and
exacerbation rates for COPD and other conditions like respiratory
infections prior to the first ICS/LABA prescription.1 Exacerbations were defined in the study as medical interventions
such
as hospitalizations, emergency room visits and prescription of oral
steroids or antibiotics due to COPD deterioration.1
The exacerbation findings published today are the first of several
analyses of the PATHOS data. As a
real-world evidence study, the findings show the impact of
the two treatment combinations in clinical practice, providing
healthcare providers, patients and payers with valuable information
that can be used to inform their treatment decisions. PATHOS also
collected data regarding rates of pneumonia events as the comparative
safety measure, the evolution of COPD care during the 11-year period
and how access to an asthma or COPD nurse impacts care. Analyses of
these data are expected in subsequent publications.
About COPD
About PATHOS
About Real-World Evidence
About SYMBICORT® (budesonide/formoterol)
About AstraZeneca
References
SOURCE AstraZeneca Canada Inc.
|
|
|||||||||||||||||||||||||||