Response to Radiotherapy After Breast-Conserving Surgery in Different Breast Cancer Subtypes in the Swedish Breast Cancer Group 91 Radiotherapy Randomized Clinical Trial

Author:

Sjöström Martin1,Lundstedt Dan1,Hartman Linda1,Holmberg Erik1,Killander Fredrika1,Kovács Anikó1,Malmström Per1,Niméus Emma1,Werner Rönnerman Elisabeth1,Fernö Mårten1,Karlsson Per1

Affiliation:

1. Martin Sjöström, Linda Hartman, Fredrika Killander, Per Malmström, Emma Niméus, and Mårten Fernö, Lund University; Martin Sjöström, Fredrika Killander, Per Malmström, and Emma Niméus, Skåne University Hospital, Lund; Dan Lundstedt, Anikó Kovács, Elisabeth Werner Rönnerman and Per Karlsson, Sahlgrenska University Hospital; Dan Lundstedt, Erik Holmberg, and Per Karlsson, University of Gothenburg; and Erik Holmberg, Regional Cancer Center West, Gothenburg, Sweden.

Abstract

Purpose To evaluate the effect of adjuvant radiotherapy (RT) after breast conservation surgery in different breast cancer subtypes in a large, randomized clinical trial with long-term follow-up. Patients and Methods Tumor tissue was collected from 1,003 patients with node-negative, stage I and II breast cancer who were randomly assigned in the Swedish Breast Cancer Group 91 Radiotherapy trial between 1991 and 1997 to breast conservation surgery with or without RT. Systemic adjuvant treatment was sparsely used (8%). Subtyping was performed with immunohistochemistry and in situ hybridization on tissue microarrays for 958 tumors. Results RT reduced the cumulative incidence of ipsilateral breast tumor recurrence (IBTR) as a first event within 10 years for luminal A–like tumors (19% v 9%; P = .001), luminal B–like tumors (24% v 8%; P < .001), and triple-negative tumors (21% v 6%; P = .08), but not for human epidermal growth factor receptor 2–positive (luminal and nonluminal) tumors (15% v 19%; P = .6); however, evidence of an overall difference in RT effect between subtypes was weak ( P = .21). RT reduced the rate of death from breast cancer (BCD) for triple-negative tumors (hazard ratio, 0.35; P = .06), but not for other subtypes. Death from any cause was not improved by RT in any subtype. A hypothesized clinical low-risk group did not have a low risk of IBTR without RT, and RT reduced the rate of IBTR as a first event after 10 years (20% v 6%; P = .008), but had no effect on BCD or death from any cause. Conclusion Subtype was not predictive of response to RT, although, in our study, human epidermal growth factor receptor 2–positive tumors seemed to be most radioresistant, whereas triple-negative tumors had the largest effect on BCD. The effect of RT in the presumed low-risk luminal A–like tumors was excellent.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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