The Influence of Adjuvant Systemic Regimens on Contralateral Breast Cancer Risk and Receptor Subtype

Author:

Kramer Iris12,Schaapveld Michael,Oldenburg Hester S A3,Sonke Gabe S4,McCool Danielle,van Leeuwen Flora E,Van de Vijver Koen K5,Russell Nicola S6,Linn Sabine C47,Siesling Sabine89,Menke-van der Houven van Oordt C Willemien10,Schmidt Marjanka K12

Affiliation:

1. Division of Molecular Pathology, The Netherlands Cancer Institute, Amsterdam, the Netherlands

2. Division of Psychosocial Research and Epidemiology, The Netherlands Cancer Institute, Amsterdam, the Netherlands

3. Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands

4. Department of Surgical Oncology

5. Department of Pathology, The Netherlands Cancer Institute, Amsterdam, the Netherlands

6. Department of Radiation Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands

7. Department of Pathology, University Medical Centre Utrecht, Utrecht, the Netherlands

8. Department of Research, Netherlands Comprehensive Cancer Organisation (IKNL), Utrecht, the Netherlands

9. Department of Health Technology and Service Research, Technical Medical Center, University of Twente, Enschede, the Netherlands

10. Department of Medical Oncology, Amsterdam UMC location VUMC, Cancer Centre Amsterdam, Amsterdam, the Netherlands

Abstract

Abstract Background An increasing number of breast cancer (BC) survivors are at risk of developing contralateral breast cancer (CBC). We aimed to investigate the influence of various adjuvant systemic regimens on, subtype-specific, risk of CBC. Methods This population-based cohort study included female patients diagnosed with first invasive BC between 2003 and 2010; follow-up was complete until 2016. Clinico-pathological data were obtained from the Netherlands Cancer Registry and additional data on receptor status through linkage with PALGA: the Dutch Pathology Registry. Cumulative incidences (death and distant metastases as competing risk) and hazard ratios (HRs) were estimated for all invasive metachronous CBC and CBC subtypes. Results Of 83 144 BC patients, 2816 developed a CBC; the 10-year cumulative incidence was 3.8% (95% confidence interval [CI] = 3.7% to 4.0%). Overall, adjuvant chemotherapy (HR = 0.70, 95% CI = 0.62 to 0.80), endocrine therapy (HR = 0.46, 95% CI = 0.41 to 0.52), and trastuzumab with chemotherapy (HR = 0.57, 95% CI = 0.45 to 0.73) were strongly associated with a reduced CBC risk. Specifically, taxane-containing chemotherapy (HR = 0.48, 95% CI = 0.36 to 0.62) and aromatase inhibitors (HR = 0.32, 95% CI = 0.23 to 0.44) were associated with a large CBC risk reduction. More detailed analyses showed that endocrine therapy statistically significantly decreased the risk of estrogen receptor (ER)-positive CBC (HR = 0.41, 95% CI = 0.36 to 0.47) but not ER-negative CBC (HR = 1.32, 95% CI = 0.90 to 1.93) compared with no endocrine therapy. Patients receiving chemotherapy for ER-negative first BC had a higher risk of ER-negative CBC from 5 years of follow-up (HR = 2.84, 95% CI = 1.62 to 4.99) compared with patients not receiving chemotherapy for ER-negative first BC. Conclusion Endocrine therapy, chemotherapy, as well as trastuzumab with chemotherapy reduce CBC risk. However, each adjuvant therapy regimen had a different impact on the CBC subtype distribution. Taxane-containing chemotherapy and aromatase inhibitors were associated with the largest CBC risk reduction.

Funder

Alpe d’HuZes/Dutch Cancer Society

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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