Poor Biological Factors and Prognosis of Interval Breast Cancers: Long-Term Results of Bahçeşehir (Istanbul) Breast Cancer Screening Project in Turkey

Author:

Cabioğlu Neslihan1,Gürdal Sibel Özkan2,Kayhan Arda3,Özaydın Nilüfer4,Şahin Cennet5,Can Ömür6,Özçınar Beyza1,Aykuter Gönül6,Vatandaş Gülçin6,Aribal Erkin7,Özmen Vahit1

Affiliation:

1. Department of Surgery, Istanbul University, Istanbul Medical Faculty, Istanbul, Turkey

2. Department of Surgery, Namık Kemal University, Faculty of Medicine, Tekirdag, Turkey

3. Department of Radiology, Erzincan Binali Yıldırım University Faculty of Medicine, Erzincan, Turkey

4. Department of Public Health, Marmara University, Faculty of Medicine, Istanbul, Turkey

5. Department of Radiology, Şişli Etfal Research and Teaching Hospital, Istanbul, Turkey

6. MEMEDER Screening Center, Bahçeşehir, Istanbul, Turkey

7. Department of Radiology, Acıbadem University, Faculty of Medicine, Istanbul, Turkey

Abstract

PURPOSE The Turkish Bahçeşehir Breast Cancer Screening Project was a 10-year, organized, population-based screening program carried out in Bahçeşehir county, Istanbul. Our aim was to examine the biologic features and outcome of screen-detected and interval breast cancers during the 10-year study period. METHODS Between 2009 and 2019, 2-view mammograms were obtained at 2-year intervals for women aged 40 to 69 years. Clinicopathological characteristics including ER, PR, HER2-neu, and Ki-67 status were analyzed for those diagnosed with breast cancer. RESULTS In 8,758 screened women, 131 breast cancers (1.5%) were detected. The majority of patients (82.3%) had prognostic stage 0-I disease. Contrarily, patients with interval cancers (n = 15; 11.4%) were more likely to have a worse prognostic stage (II-IV disease; odds ratio [OR], 3.59, 95% CI, 0.9 to 14.5) and high Ki-67 scores (OR, 3.14; 95% CI, 0.9 to 11.2). Interval cancers detected within 1 year were more likely to have a luminal B (57.1% v 31.9%) and triple-negative (14.3% v 1%) subtype and less likely to have a luminal A subtype (28.6% v 61.5%; P = .04). Patients with interval cancers had a poor outcome in 10-year disease-specific (DSS) and disease-free survival (DFS) compared with those with screen-detected cancers (DSS: 68.2% v 98.1%, P = .002; DFS: 78.6% v 96.5%, P = .011). CONCLUSION Our findings suggest the majority of screen-detected breast cancers exhibited a luminal A subtype profile with an excellent prognosis. However, interval cancers were more likely to have aggressive subtypes such as luminal B subtype or triple-negative cancers associated with a poor prognosis requiring other preventive strategies.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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