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指南变化对随机对照 HYPOSIB 试验中采用 Hypofractionation 和乳腺癌患者特征的影响。

Impact of guideline changes on adoption of hypofractionation and breast cancer patient characteristics in the randomized controlled HYPOSIB trial.

机构信息

Klinik für Strahlentherapie, Universitätsklinikum Schleswig-Holstein Campus Kiel, Arnold-Heller-Str. 3, 24105, Kiel, Germany.

Institut für Medizinische Biometrie und Statistik, Universität zu Lübeck, Universitätsklinikum Schleswig-Holstein, Lübeck, Germany.

出版信息

Strahlenther Onkol. 2021 Sep;197(9):802-811. doi: 10.1007/s00066-020-01730-9. Epub 2020 Dec 15.

Abstract

PURPOSE

Hypofractionated radiotherapy is the standard of care for adjuvant whole breast radiotherapy (RT). However, adoption has been slow. The indication for regional nodal irradiation has been expanded to include patients with 0-3 involved lymph nodes. We investigated the impact of the publication of the updated German S3 guidelines in 2017 on adoption of hypofractionation and enrollment of patients with lymph node involvement within a randomized controlled phase III trial.

METHODS

In the experimental arm of the HYPOSIB trial (NCT02474641), hypofractionated RT with simultaneous integrated boost (SIB) was used. In the standard arm, RT could be given as hypofractionated RT with sequential boost (HF), normofractionated RT with sequential boost (NF), or normofractionated RT with SIB (NF). The cutoff date for the updated German S3 guidelines was December 17, 2017. Temporal trends were analyzed by generalized linear regression models. Multiple logistic regression models were used to investigate the influence of time (prior to/after guideline) and setting (university hospital/other institutions) on the fractionation patterns.

RESULTS

Enrollment of patients with involved lymph nodes was low throughout the trial. Adoption of HF increased over time and when using the guideline publication date as cutoff. Results of the multiple logistic regressions showed an interaction between time and setting. Furthermore, the use of HF was significantly more common in university hospitals.

CONCLUSION

The use of HF in the standard arm increased over the course of the HYPOSIB trial and after publication of the S3 guideline update. This was primarily driven by patients treated in university hospitals. Enrolment of patients with lymph node involvement was low throughout the trial.

摘要

目的

适形分割放射治疗是辅助全乳放射治疗(RT)的标准治疗方法。然而,其应用进展缓慢。区域淋巴结照射的适应证已扩大到包括 0-3 个受累淋巴结的患者。我们研究了 2017 年德国 S3 指南更新的发布对接受适形分割和纳入随机对照 III 期试验中淋巴结受累患者的影响。

方法

在 HYPOSIB 试验的实验组(NCT02474641)中,采用了同步整合boost 的适形分割放疗(SIB)。在标准组中,RT 可以采用适形分割放疗序贯boost(HF)、常规分割放疗序贯boost(NF)或常规分割放疗 SIB(NF)。德国 S3 指南更新的截止日期为 2017 年 12 月 17 日。采用广义线性回归模型分析时间趋势。采用多逻辑回归模型研究时间(指南发布前/后)和环境(大学医院/其他机构)对分割模式的影响。

结果

试验期间,淋巴结受累患者的入组率一直较低。HF 的应用随着时间的推移而增加,且以指南发布日期为截止日期时更是如此。多逻辑回归模型的结果显示,时间和环境之间存在交互作用。此外,HF 的使用在大学医院更为常见。

结论

在 HYPOSIB 试验期间及 S3 指南更新发布后,标准组中 HF 的应用逐渐增加。这主要是由在大学医院接受治疗的患者推动的。试验期间,淋巴结受累患者的入组率一直较低。

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