Abstract

PurposeOur purpose was to explore the prognosis of aggressive breast cancers of the HER2 oncogene amplification (HER2 +) and triple-negative (TN) subtypes detected by screening, as well as the prognosis of interval cancers (clinically due to symptoms between screening rounds) and cancers in screening nonparticipants.MethodsThe study population comprised of 823 breast cancers in women aged 50–69 years from 2006–2014. Of these, 572 were found by screening mammography (69%), 170 were diagnosed between the screening rounds (21%), and 81 were diagnosed in women who did not participate in the screening program (10%).ResultsThe majority of all HER2 + (59%) and TN cancers (57%) in this age group were detected by screening. Screen-detected HER2 + tumors were small (median 12 mm), and node-negative (84%). During a median follow-up of eight years, the distant disease-free survival of screen-detected HER2 + and TN cancers was better than that of interval and nonparticipant cancers (age-adjusted HR = 0.16, 95% CI 0.03–0.81 and HR = 0.09, 95% CI 0.01–0.79, respectively). In nonparticipants, the distant disease-free survival of these cancers was worse than in participants (age-adjusted HR = 2.52, 95% CI 0.63–10.11 and HR = 5.30, 95% 1.16–24.29, respectively).ConclusionIn the 50–69 age group, the majority of HER2 + and TN cancers can be found by a quality assured population-based mammography screening. Despite their generally aggressive behavior, after a median follow-up of 8 years, distant disease-free survival was over 90% of these cancers detected by screening. The worst prognosis of these cancers was in women who did not participate in screening.

Highlights

  • Breast cancer screening aims to reduce mortality by allowing diagnosis before disease dissemination

  • We aimed to explore the prognosis of HER2 + or TN breast cancers found by screening and by symptoms between two screening rounds and in women of screening age (50–69 years) who did not participate in screening

  • The majority of screen-detected breast cancers (SDBCs) were smaller than 2 cm pT1 (82%) and node-negative pN0 (69%), while the proportions were smaller for IBCs and NSBCs

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Summary

Introduction

Breast cancer screening aims to reduce mortality by allowing diagnosis before disease dissemination. Screen-detected breast cancers (SDBCs) are smaller and less commonly spread to the axillary lymph nodes, which is partly an advantage gained by screening. Breast Cancer Research and Treatment (2021) 187:267–274 and lead time [1,2,3]. Within the biological spectrum of breast cancers, those displaying gene amplification of human epidermal growth factor receptor 2 (HER2 +) and those that are triple-negative (TN, i.e., negative for ER, PR and HER2) are generally considered biologically aggressive tumor subtypes. For HER2 + breast cancer, the prognosis has improved due to the introduction of targeted therapies [7,8,9]. For TN breast cancer, no targeted oncological treatments are currently available. TN patients are treated with surgery, radiation, and chemotherapy [10]

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