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Outcome switching in randomized controlled oncology trials reporting on surrogate endpoints: a cross-sectional analysis
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AbstractInconsistent reporting of clinical trials is well-known in the literature. Despite this, factors associated with poor practice such as outcome switching in clinical trials are poorly understood. We performed a cross-sectional analysis to evaluate the prevalence of, and the factors associated with outcome switching. PubMed and Embase were searched for pharmaceutical randomized controlled trials (RCTs) in oncology reporting on a surrogate primary outcome published in 2015. Outcome switching was present in 18% (39/216). First-author male sex was significantly more likely associated with outcome switching compared to female sex with an OR of 3.05 (95% CI 1.07–8.64,p = 0.04) after multivariable adjustment. For-profit funded RCTs were less likely associated with outcome switching compared to non-profit funded research with an OR of 0.22 (95% CI 0.07–0.74,p = 0.01). First author male sex was more likely associated with outcome switching compared to female sex in drug oncology RCTs reporting on a primary surrogate endpoint. For-profit funded research was less likely associated with outcome switching compared to research funded by non-profit organizations. Furthermore, 18 percent of drug oncology trials reporting on a surrogate endpoint could have a higher risk of false positive results due to primary outcome switching.
Springer Science and Business Media LLC
Title: Outcome switching in randomized controlled oncology trials reporting on surrogate endpoints: a cross-sectional analysis
Description:
AbstractInconsistent reporting of clinical trials is well-known in the literature.
Despite this, factors associated with poor practice such as outcome switching in clinical trials are poorly understood.
We performed a cross-sectional analysis to evaluate the prevalence of, and the factors associated with outcome switching.
PubMed and Embase were searched for pharmaceutical randomized controlled trials (RCTs) in oncology reporting on a surrogate primary outcome published in 2015.
Outcome switching was present in 18% (39/216).
First-author male sex was significantly more likely associated with outcome switching compared to female sex with an OR of 3.
05 (95% CI 1.
07–8.
64,p = 0.
04) after multivariable adjustment.
For-profit funded RCTs were less likely associated with outcome switching compared to non-profit funded research with an OR of 0.
22 (95% CI 0.
07–0.
74,p = 0.
01).
First author male sex was more likely associated with outcome switching compared to female sex in drug oncology RCTs reporting on a primary surrogate endpoint.
For-profit funded research was less likely associated with outcome switching compared to research funded by non-profit organizations.
Furthermore, 18 percent of drug oncology trials reporting on a surrogate endpoint could have a higher risk of false positive results due to primary outcome switching.
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