2015
DOI: 10.1093/annonc/mdu360
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Guidelines for time-to-event end point definitions in sarcomas and gastrointestinal stromal tumors (GIST) trials: results of the DATECAN initiative (Definition for the Assessment of Time-to-event Endpoints in CANcer trials)

Abstract: Background: The use of potential surrogate end points for overall survival, such as disease-free survival (DFS) or time- of time-to-event (TTE) end points is rarely precise and lacks uniformity across trials. End point definition can impact trial results by affecting estimation of treatment effect and statistical power. The DATECAN initiative (Definition for the Assessment of Time-to-event End points in CANcer trials) aims to provide recommendations for definitions of TTE end points. We report guidelines for … Show more

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Cited by 41 publications
(28 citation statements)
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“…In the paper published by Desiderio et al . , five patients with a mean age of 63.6 years (43–76) underwent robotic surgical resection for gastric GIST. Lesions were localized to the anterior wall of the gastric antrum in two patients and near the pyloric area in the other three.…”
Section: Resultsmentioning
confidence: 99%
“…In the paper published by Desiderio et al . , five patients with a mean age of 63.6 years (43–76) underwent robotic surgical resection for gastric GIST. Lesions were localized to the anterior wall of the gastric antrum in two patients and near the pyloric area in the other three.…”
Section: Resultsmentioning
confidence: 99%
“…Progression‐free interval (PFI) was calculated for all dogs and defined as the time from the day of first toceranib treatment to the time of disease progression (defined as local recurrence, local progression, metastasis, or some combination of these), the time of death from any cause, or the time of data collection . For dogs with gross (measurable) disease, as in previous publications describing the use of toceranib in dogs, clinical benefit (CB) was determined by best response to treatment and was defined as complete response (CR) or partial response (PR) of any duration, or stable disease (SD) of at least 10 weeks in duration .…”
Section: Methodsmentioning
confidence: 99%
“…For ''cause of mortality" ascertained cases, misclassification is still possible during the study period with the interplay of disease recurrence, emergence of second primaries, treatment related toxicity, and other intercurrent diseases relevant to such patients. Bellera et al [38] recommended classifying cause of death into 5 categories in clinical trials according to: a). primary cancer/to progression, b).…”
Section: Discussionmentioning
confidence: 99%