2011
DOI: 10.1016/j.ijrobp.2010.05.011
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Outcomes After Accelerated Partial Breast Irradiation in Patients With ASTRO Consensus Statement Cautionary Features

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Cited by 56 publications
(26 citation statements)
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“…Other series similarly showed a 0% 5-year IBTR risk among 32 women with DCIS treated with multicatheter brachytherapy. 18 In contrast, one single-institution investigation reported a trend toward higher risk of time to IBTR among pure DCIS tumors compared with invasive ductal carcinomas at 4 years after MammoSite (hazard ratio, 3.57; P = .06). 19 One prospective multicenter trial using MammoSite in 41 DCIS patients showed a 9.8% 5-year risk of IBTR, all outside the treatment field.…”
Section: Pure Dcismentioning
confidence: 89%
“…Other series similarly showed a 0% 5-year IBTR risk among 32 women with DCIS treated with multicatheter brachytherapy. 18 In contrast, one single-institution investigation reported a trend toward higher risk of time to IBTR among pure DCIS tumors compared with invasive ductal carcinomas at 4 years after MammoSite (hazard ratio, 3.57; P = .06). 19 One prospective multicenter trial using MammoSite in 41 DCIS patients showed a 9.8% 5-year risk of IBTR, all outside the treatment field.…”
Section: Pure Dcismentioning
confidence: 89%
“…The groupings were based primarily on an analysis of the characteristics of patients most frequently included in trials of APBI and not on data that identified subsets of patients with higher rates of ipsilateral breast tumor recurrence (IBTR) when treated with APBI. Recent analysis using ASBS registry trial [139,140] and using data from using of University of Wisconsin [141] show that the ASTRO consensus groupings may not be optimal in identifying patients for APBI.…”
Section: Discussionmentioning
confidence: 99%
“…7,88,89 The NSABP/ RTOG trial should help shine some light on the growing number of groups with data that does not correlate well with the expected outcomes of the ASTRO consensus statement groupings, [76][77][78][79][80][81] and our current understanding of appropriate patient selection criteria. The trial is closed to low-risk groupings, having accrued 4,169 patients as of October 2012 of the needed 4,300 to complete accrual.…”
Section: Discussion Of Datamentioning
confidence: 99%