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首页> 外文期刊>BMC Cancer >Adjuvant trastuzumab duration trials in HER2 positive breast cancer – what results would be practice-changing? Persephone investigator questionnaire prior to primary endpoint results
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Adjuvant trastuzumab duration trials in HER2 positive breast cancer – what results would be practice-changing? Persephone investigator questionnaire prior to primary endpoint results

机译:HER2阳性乳腺癌辅助曲妥珠单抗持续时间试验–什么结果将改变实践?主要终点结果之前的Persephone调查员问卷

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Twelve months treatment is the current standard of care for adjuvant trastuzumab in patients with HER2 positive early breast cancer however the optimal duration is not known. Persephone is a non-inferiority randomised controlled trial comparing 6- to 12-months of trastuzumab. In this trial there will be a trade-off between a possible small decrease in disease-free survival (DFS) with 6-months and reduced cardiotoxicity and cost. A structured questionnaire asked clinicians who had recruited patients into the Persephone trial about their prior beliefs with regards to the clinical effectiveness of trastuzumab and cardiotoxicity profile, in the comparison of 6- and 12-month durations. Fifty-one clinicians from 40 of the 152 Persephone sites completed the questionnaire. 30/50 responders (60%) believed that 6-months trastuzumab would give the same 4-year DFS rate as 12-months trastuzumab, with 21/50 (42%) holding this belief across all breast cancer subsets. In addition, 46/49 responders (94%) reported expecting to change their clinical practice to 6-months, with their prior beliefs (most commonly 85% 4-year DFS rate with 6-months) being greater than their lowest acceptable rate (most commonly 83% 4-year DFS rate with 6-months). Low levels of cardiotoxicity were expected with both 6 and 12-months trastuzumab, with the majority expecting lower levels with 6-months. With increasing hypothesised differences of cardiotoxicity rates between the two durations, significantly lower levels of 4-year DFS with 6-months trastuzumab were deemed acceptable (p?
机译:十二个月的治疗是HER2阳性早期乳腺癌患者辅助曲妥珠单抗的当前治疗标准,但是最佳治疗时间尚不清楚。 Persephone是一项非劣效性随机对照试验,比较了曲妥珠单抗6到12个月的情况。在该试验中,将有可能在6个月的无病生存期(DFS)小幅下降与降低的心脏毒性和成本之间进行权衡。一份结构化的问卷调查询问了招募参加Persephone试验的患者的临床医生,他们比较了6个月和12个月的持续时间有关曲妥珠单抗的临床有效性和心脏毒性特征。 152个Persephone网站中的40个网站的五十一个临床医生完成了调查问卷。 30/50的响应者(60%)认为6个月的曲妥珠单抗将与12个月的曲妥珠单抗提供相同的4年DFS率,其中21/50(42%)的所有乳腺癌亚组都持有这一信念。此外,有46/49位回应者(94%)表示希望将他们的临床实践更改为6个月,他们先前的信念(最常见的是6个月的4年DFS率为85%)大于其最低接受率(最常见的是4年DFS率为83%,为期6个月)。预计曲妥珠单抗6个月和12个月的心脏毒性水平较低,而大多数人预计6个月的心脏毒性水平较低。随着两个疗程之间心脏毒性率假说差异的增加,认为接受曲妥珠单抗6个月的4年DFS水平明显降低是可以接受的(p≤0.0001)。大多数响应者认为,在总体上以及在每个乳腺癌亚组中,曲妥珠单抗治疗6个月就足够了,如果Persephone的结果支持他们先前的信念,他们计划改变其临床实践。对持续时间试验的个体患者荟萃分析可以更准确地估计功效和毒性的差异,并具有足够的统计能力来确定6个月辅助曲妥珠单抗的2%的非劣效性。

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