2010
DOI: 10.1200/jco.2010.28.15_suppl.5508
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Postoperative accelerated radiotherapy (POPART) versus conventional postoperative radiotherapy (CPORT) in squamous cell head and neck cancer: A multicenter prospective randomized study of the Dutch Head and Neck Cooperative Study Group.

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Cited by 5 publications
(7 citation statements)
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“…The control group of a four-arm trial 4 was triplicated (ie, data for patients in the control group were copied twice to have three control arms to compare with each experimental arm), a 2 × 2 trial (EORTC 22962 45 ) included three relevant comparisons for the meta-analysis, and three three-arm trials 36,37,55 included two relevant comparisons. The 33 trials included in the analysis of fractionation schedules (comparison 1) were divided into four predefined subgroups, depending on the type of radiotherapy: hyperfractionation (eight comparisons, including the unpublished EORTC 22962 trial), 4,33,44,45,49,50,56 moderately accelerated radiotherapy (19 comparisons), 2,4,30,32,3439,41,42,46,54,55,5759 very accelerated radiotherapy (seven comparisons, including the unpublished CHARTWEL trial), 3,47,5153,60 and moderately hypofractionated (dose per fraction between 2–2·5 Gy [two comparisons]; 31,40 appendix pp 17–18). After discussion with the steering committee, the moderately hypofractionated trials were included in the moderately accelerated radiotherapy group.…”
Section: Resultsmentioning
confidence: 99%
“…The control group of a four-arm trial 4 was triplicated (ie, data for patients in the control group were copied twice to have three control arms to compare with each experimental arm), a 2 × 2 trial (EORTC 22962 45 ) included three relevant comparisons for the meta-analysis, and three three-arm trials 36,37,55 included two relevant comparisons. The 33 trials included in the analysis of fractionation schedules (comparison 1) were divided into four predefined subgroups, depending on the type of radiotherapy: hyperfractionation (eight comparisons, including the unpublished EORTC 22962 trial), 4,33,44,45,49,50,56 moderately accelerated radiotherapy (19 comparisons), 2,4,30,32,3439,41,42,46,54,55,5759 very accelerated radiotherapy (seven comparisons, including the unpublished CHARTWEL trial), 3,47,5153,60 and moderately hypofractionated (dose per fraction between 2–2·5 Gy [two comparisons]; 31,40 appendix pp 17–18). After discussion with the steering committee, the moderately hypofractionated trials were included in the moderately accelerated radiotherapy group.…”
Section: Resultsmentioning
confidence: 99%
“…The NCDB does not provide data on local‐regional control, which would have been another useful outcome in this study. The use of accelerated RT was not examined in this study, although previous trials show no local‐regional control or survival benefit with the use of accelerated RT in the adjuvant setting …”
Section: Discussionmentioning
confidence: 99%
“…Published hazard ratios and hazard ratios extracted from available survival curves were the basis of the meta-analysis. Additionally, we extracted and categorized the published acute and late side effects from the published papers [ 6 11 , 18 , 19 ]. The idea for this meta-analysis was originally generated in 2016.…”
Section: Methodsmentioning
confidence: 99%
“…These observations allow an investigation of accelerated schedules in the postoperative setting and to the best of our knowledge no meta-analysis has focused on this aspect yet. The results of six randomized trials addressing this question in adjuvant RT were retrieved and analyzed [ 6 11 , 18 ].…”
Section: Introductionmentioning
confidence: 99%