In confirmatory cancer clinical trials, overall survival (OS) is normally a primary endpoint in the intention-to-treat (ITT) analysis under regulatory standards. After the tumor progresses, it is common that patients allocated to the control group switch to the experimental treatment, or another drug in the same class. Such treatment switching may dilute the relative efficacy of the new drug compared to the control group, leading to lower statistical power. It would be possible to decrease the estimation bias by shortening the follow-up period but this may lead to a loss of information and power. Instead we propose a modified weighted log-rank test (mWLR) that aims at balancing these factors by down-weighting events occurring when many pati...
Objectives: To systematically review the quality of reporting on the application of switching adjust...
Abstract Background Treatment switching is common in randomised trials of oncology treatments, with ...
The major end-points arising from cancer clinical trials are reviewed. These are: tumour response, t...
In confirmatory cancer clinical trials, overall survival (OS) is normally a primary endpoint in the ...
This paper evaluates the loss of power of the simple and stratified logrank tests due to heterogenei...
Background: A common feature of many recent trials evaluating the effects of immunotherapy on surviv...
Nonproportional hazards (NPH) have been observed in confirmatory clinical trials with time to event ...
When patients randomised to the control group of a randomised controlled trial are allowed to switch...
Non-proportional hazards have been observed in clinical trials. The log-rank test loses power and th...
The log-rank test is a cornerstone of phase III oncology clinical trials. However, there are at leas...
Background: It is not uncommon for clinical trials to present results on survival time as Kaplan-Me...
1noProportional hazards are a common assumption when designing confirmatory clinical trials in onco...
BACKGROUND: Treatment switching is common in randomised trials of oncology treatments, with control ...
International audienceComparing survival functions with the log-rank test in the presence of depende...
Background Treatment switching is common in randomised trials of oncology treatments, with control ...
Objectives: To systematically review the quality of reporting on the application of switching adjust...
Abstract Background Treatment switching is common in randomised trials of oncology treatments, with ...
The major end-points arising from cancer clinical trials are reviewed. These are: tumour response, t...
In confirmatory cancer clinical trials, overall survival (OS) is normally a primary endpoint in the ...
This paper evaluates the loss of power of the simple and stratified logrank tests due to heterogenei...
Background: A common feature of many recent trials evaluating the effects of immunotherapy on surviv...
Nonproportional hazards (NPH) have been observed in confirmatory clinical trials with time to event ...
When patients randomised to the control group of a randomised controlled trial are allowed to switch...
Non-proportional hazards have been observed in clinical trials. The log-rank test loses power and th...
The log-rank test is a cornerstone of phase III oncology clinical trials. However, there are at leas...
Background: It is not uncommon for clinical trials to present results on survival time as Kaplan-Me...
1noProportional hazards are a common assumption when designing confirmatory clinical trials in onco...
BACKGROUND: Treatment switching is common in randomised trials of oncology treatments, with control ...
International audienceComparing survival functions with the log-rank test in the presence of depende...
Background Treatment switching is common in randomised trials of oncology treatments, with control ...
Objectives: To systematically review the quality of reporting on the application of switching adjust...
Abstract Background Treatment switching is common in randomised trials of oncology treatments, with ...
The major end-points arising from cancer clinical trials are reviewed. These are: tumour response, t...