4.3 Article

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

Journal

STRAHLENTHERAPIE UND ONKOLOGIE
Volume 197, Issue 9, Pages 802-811

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00066-020-01730-9

Keywords

Guideline implementation; Breast cancer; Radiotherapy; Hypofractionation

Funding

  1. Stiftung Deutsche Krebshilfe (German Cancer Aid) [110897]

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The study examined the impact of the 2017 update of the German S3 guidelines on adoption of hypofractionation and enrollment of patients with lymph node involvement in a randomized controlled phase III trial. The results showed an increase in adoption of hypofractionated radiotherapy and particularly in university hospitals, while enrollment of patients with lymph node involvement remained low throughout the trial.
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 (HFseq), normofractionated RT with sequential boost (NFseq), or normofractionated RT with SIB (NFSIB). 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 HFseq 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 HFseq was significantly more common in university hospitals. Conclusion The use of HFseq 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.

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