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. 2021 Aug;26(8):e1372-e1380.
doi: 10.1002/onco.13813. Epub 2021 Jun 1.

Real-World Clinical Outcomes in Biological Subgroups of Breast Cancer in the Hospital District of Southwest Finland

Affiliations

Real-World Clinical Outcomes in Biological Subgroups of Breast Cancer in the Hospital District of Southwest Finland

Heli Teerenhovi et al. Oncologist. 2021 Aug.

Abstract

Background: Comparing breast cancer survival trends globally, Finland is among the top three countries in Europe. However, outcome data on breast cancer subgroups in the Finnish population are limited. This retrospective, registry-based study aimed to assess patient characteristics and clinical outcomes of different breast cancer subgroups in early (EBC) and metastatic breast cancer (MBC) in a real-life clinical setting.

Materials and methods: The study consisted of 6,977 adult, female patients with breast cancer diagnosed in Southwest Finland during 2005-2018. Patients were divided into four mutually exclusive groups: human epidermal growth factor receptor 2 positive (HER2+), triple negative, HER2-/hormone receptor positive (HR+), and HER2 and/or HR status unknown, and further into patients with EBC and MBC. Overall survival (OS) was assessed as a clinical outcome, as well as the following real-world (rw) clinical outcomes: disease-free survival (rwDFS), progression-free survival (rwPFS), and distant recurrence-free interval (rwDRFI).

Results: Within EBC, 5-year survival was the highest (88%) in HER2-/HR+, followed by 85% in HER2+, and 75% in triple negative. The rwDFS varied significantly in EBC (5-year rwDFS HER2 -/HR+, HER2+, triple negative: 87%, 80%, 71% respectively). In MBC, median survival was 2 years for both HER2-/HR+ and HER2+ and markedly shorter for triple negative (0.8 years). Independent predictors of mortality were age (hazard ratio [HR], 1.1), other subgroups than HER2-/HR+ (HR, 1.2-1.9), metastatic disease (HR, 9.8), and other malignancies (HR, 2.7).

Conclusion: This registry-based study demonstrates significant differences in breast cancer outcomes on the subgroup level, as well as poorer outcomes compared with clinical trials, giving complementary insight on clinical characteristics in an unselected patient population.

Implications for practice: This retrospective, registry-based study assessed the clinical outcomes of different breast cancer subgroups in 6,977 adult, female patients with breast cancer diagnosed in Southwest Finland during 2005-2018. Results demonstrated significant variation in the survival between subgroups in both early breast cancer and metastatic breast cancer, as well as differences between unselected patients representing the standard of care and randomized clinical trials. Although, according to the global comparison of survival trends, the net survival of patients with breast cancer in Finland is generally high, there is great variation between subgroups. These real-life breast cancer data provide tools to further evaluate medical need in different breast cancer subgroups.

Keywords: Breast cancer; Clinical outcomes; Real-world evidence; Registry-study; Subgroups.

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Conflict of interest statement

Disclosures of potential conflicts of interest may be found at the end of this article.

Figures

Figure 1
Figure 1
rwDFS in early, and rwPFS in metastatic breast cancer. Kaplan‐Meier curves of rwDFS in early breast cancer (A), and rwPFS in metastatic breast cancer (B). The p value at the top right corners of each panel indicate the significance from log‐rank test for the difference in survival rates among the subgroups. Abbreviations: HER2+, human epidermal growth receptor 2 positive; HR, hormone receptor; NA, not available; rwDFS, real‐world disease‐free survival; rwPFS, real‐world progression‐free survival.
Figure 2
Figure 2
OS in early and metastatic breast cancer. OS stratified by biological subgroup in patients with early breast cancer (A), and in patients with metastatic breast cancer (B). The p values at the top right corners of each panel indicate the significance from log‐rank test for the difference in survival rates among the subgroups. Dashed black lines in (B) indicate the median survival times. Abbreviations: HER2+, human epidermal growth receptor 2 positive; HR, hormone receptor; NA, not available; OS, overall survival.
Figure 3
Figure 3
rwDRFI in early breast cancer. Kaplan‐Meier fit of rwDRFI stratified by biological subgroup in patients with early breast cancer. The p value above the survival curves indicates the significance from log‐rank test for the difference in metastasis development probabilities among the subgroups. Abbreviations: HER2+, human epidermal growth receptor 2 positive; HR, hormone receptor; NA, not available; rwDRFI, real‐world distant recurrence‐free interval.

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