Author(s): Birgitte V. Offersen, MD, PhD1,2,3; Jan Alsner, PhD1; Kristine Høgsbjerg, PhD1; Hanne M. Nielsen, PhD3; Else Maae, PhD4; Mette H. Nielsen, PhD5; Ingvil Mjaaland, MD6; Maja V. Maraldo, PhD7; Carine Kirkove, MD8; Tamas Lörincz, MD9; Sami Al-Rawi, MD10; Egil S. Blix, PhD11,12; Andreas Schreiber, MD13; Mechthild Krause, PhD14,15,16,17,18; Unn-Miriam Kasti, MD19; Louise W. Matthiessen, PhD20; Camilla Kronborg, PhD21; Trine Tramm, PhD22; Maj-Britt Jensen, DMSc23; Jens Overgaard, DMSc1; on behalf of the DBCG RT Committee;
PURPOSE
Adjuvant radiotherapy for node-positive breast cancer (BC) using 50Gy/25fx has been Danish Breast Cancer Group (DBCG) standard. Hypofractionated radiotherapy based on 40Gy/15fx has been increasingly used; however, it is less frequently for locoregional therapy because of concern over more morbidity. DBCG Skagen trial 1 hypothesized that 40Gy/15fx did not cause more lymphedema than 50Gy/25fx 3 years after radiotherapy without compromising the pattern of failure.
METHODS
Skagen trial 1 is a phase III, noninferiority trial randomly assigning high-risk BC patients with an indication for locoregional radiotherapy to standard 50Gy/25fx versus experimental 40Gy/15fx. The primary end point was arm lymphedema; assuming a 3-year incidence with 50Gy/25fx of 10%, noninferiority was predefined to maximum 5% excess incidence with 40Gy/15fx. Accrual continued until 3-year estimates were reported in 1,012 patients.
RESULTS
Between 2015 and 2021, 2,963 patients consented from 17 centers; the intention-to-treat cohort comprised 2,908 patients: 1,444 had 50Gy (50%), and 1,464 had 40Gy (50%). The median age was 57 years (range, 23-86). a median follow-up of 4.1 years (IQR, 3.0-5.0), the 3-year rates of lymphedema were 9.4% (50Gy) versus 8.0% (40Gy), odds ratio 0.84 (95% CI, 0.62 to 1.14), and P = .27, thus within the +5-percentage-point noninferiority margin. The median follow-up for cancer outcomes was 5.25 years (IQR, 4.26 to 6.96). Within 8 years, the hazard ratio for locoregional recurrence was 0.96 (95% CI, 0.62 to 1.51), that for distant recurrence was 1.10 (95% CI, 0.89 to 1.37), that for BC mortality was 1.25 (95% CI, 0.93 to 1.66), and that for all-cause mortality was 1.08 (95% CI, 0.85 to 1.36), thus all with no differences by random assignment.
CONCLUSION
40Gy/15fx for locoregional radiotherapy of BC did not result in more lymphedema compared with 50Gy/25fx. There were no differences in locoregional or distant recurrences, breast cancer mortality, nor all-cause mortality between the random assignment arms.
Author Affiliations
1Department of Experimental Clinical Oncology, Aarhus University Hospital, Aarhus, Denmark; 2Aarhus University, Aarhus, Denmark; 3Department of Oncology, Aarhus University Hospital, Aarhus, Denmark; 4Department of Oncology, Lillebaelt Hospital, Vejle, Denmark; 5Department of Oncology, Odense University Hospital, Odense, Denmark; 6Department of Oncology, Stavanger University Hospital, Stavanger, Norway; 7Department of Oncology, Rigshospitalet, Copenhagen, Denmark; 8Université Catholique de Louvain, Cliniques Universitaires St-Luc, Radiotherapy Department, Bruxelles, Belgium; 9Department of Oncology, Aalborg University Hospital, Aalborg, Denmark; 10Department of Oncology, Zealand University Hospital, Roskilde, Denmark; 11Department of Clinical Medicine, UiT, The Arctic University of Norway, Tromsø, Norway; 12Department of Oncology, University Hospital of North Norway, Tromsø, Norway; 13Department of Oncology, Academic Teaching Hospital Dresden-Friedrichstadt, Dresden, Germany; 14Department of Radiation Oncology and OncoRay, University Hospital and Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany; 15German Cancer Consortium (DKTK), Dresden, Germany; 16Helmholtz-Zentrum Dresden—Rossendorf, Dresden, Germany; 17National Center for Tumor Diseases (NCT), Dresden, Germany; 18German Cancer Research Center (DKFZ), Heidelberg, Germany; 19Department of Oncology, Hospital of Kristiansand, Kristiansand, Norway; 20Department of Oncology, Herlev and Gentofte University Hospital, Herlev, Denmark; 21Danish Centre for Particle Therapy, Aarhus, Denmark; 22Department of Pathology, Aarhus University Hospital, Aarhus, Denmark; 23Department of Oncology, Danish Breast Cancer Group, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark