In medical oncology randomized trials, treatment effect is usually assessed on several endpoints, including one or more time-to-event endpoints. An overall analysis of the treatment effect may include the outcomes observed on all the relevant endpoints. A systematic review of medical oncology phase III trials was conducted. We extracted the methods used to record, analyze and report adverse events and patient-reported outcomes. Our findings show that some methodological aspects of adverse events or patient-reported outcomes collection and analysis were poorly reported. Even when reported, the methods used were highly heterogeneous. Another objective was to develop an extension of the generalized pairwise comparison procedure for time-to-eve...
Randomized controlled clinical trials play an important role in the development of new medical thera...
Le nombre croissant d’essais cliniques pour le traitement du cancer a conduit à la standardisation d...
In oncology clinical trials, progression-free survival (PFS), generally defined as the time from ran...
In medical oncology randomized trials, treatment effect is usually assessed on several endpoints, in...
Treatment effects are assessed in clinical trials on multiple endpoints independently and without al...
In survival analysis with competing risks, the treatment effect is typically expressed using cause-s...
Abstract Background In randomised clinical trials involving time-to-event outcomes, the failures con...
Les effets des traitements sont évalués dans des essais cliniques sur plusieurs critères de jugement...
The primary scientific goal of a randomized clinical trial of two treatments, A and B, is to compare...
International audienceGeneralized pairwise comparisons have been proposed to permit a comprehensive ...
La survie globale (SG) est considérée comme le critère de jugement principal de référence et le plus...
OBJECTIVE: The assessment of benefits and harms from experimental treatments often ignores the assoc...
The purpose/aim of this thesis is to contribute to the analysis and comparison of PROs (« patient-re...
none7siBACKGROUND: One aim of personalized medicine is to determine which treatment is to be prefe...
Assessing the effectiveness of cancer treatments in clinical trials raises multiple methodological p...
Randomized controlled clinical trials play an important role in the development of new medical thera...
Le nombre croissant d’essais cliniques pour le traitement du cancer a conduit à la standardisation d...
In oncology clinical trials, progression-free survival (PFS), generally defined as the time from ran...
In medical oncology randomized trials, treatment effect is usually assessed on several endpoints, in...
Treatment effects are assessed in clinical trials on multiple endpoints independently and without al...
In survival analysis with competing risks, the treatment effect is typically expressed using cause-s...
Abstract Background In randomised clinical trials involving time-to-event outcomes, the failures con...
Les effets des traitements sont évalués dans des essais cliniques sur plusieurs critères de jugement...
The primary scientific goal of a randomized clinical trial of two treatments, A and B, is to compare...
International audienceGeneralized pairwise comparisons have been proposed to permit a comprehensive ...
La survie globale (SG) est considérée comme le critère de jugement principal de référence et le plus...
OBJECTIVE: The assessment of benefits and harms from experimental treatments often ignores the assoc...
The purpose/aim of this thesis is to contribute to the analysis and comparison of PROs (« patient-re...
none7siBACKGROUND: One aim of personalized medicine is to determine which treatment is to be prefe...
Assessing the effectiveness of cancer treatments in clinical trials raises multiple methodological p...
Randomized controlled clinical trials play an important role in the development of new medical thera...
Le nombre croissant d’essais cliniques pour le traitement du cancer a conduit à la standardisation d...
In oncology clinical trials, progression-free survival (PFS), generally defined as the time from ran...