4.5 Article

New brain metastases after whole-brain radiotherapy of initial brain metastases in breast cancer patients: the significance of molecular subtypes (KROG 16-12)

Journal

BREAST CANCER RESEARCH AND TREATMENT
Volume 186, Issue 2, Pages 453-462

Publisher

SPRINGER
DOI: 10.1007/s10549-020-06043-0

Keywords

Brain-directed treatment; Brain metastasis; Breast cancer; Tumor molecular subtype; Whole-brain radiotherapy

Categories

Funding

  1. Ministry of Science and Information & Communication Technology (NRF) [2017M2A2A7A01018438]
  2. SNUBH Research Fund [14-29190310]
  3. National Research Foundation of Korea [2017M2A2A7A01018438] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The study identified risk factors leading to new brain metastases following brain-directed treatment for initial metastases from breast cancer. Different tumor molecular subtypes were associated with rates of new brain metastases development and effectiveness of initial whole-brain radiotherapy, with anti-HER2 therapy significantly reducing new brain metastases in HER2+ patients.
Purpose To identify the risk factors leading to new brain metastases (BM) following brain-directed treatment for initial BM resulting from breast cancer (BC). Methods In this multi-institutional study, 538 BC patients with available follow-up imaging after brain-directed treatment for initial BM were analyzed. Tumor molecular subtypes were classified as follows: hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-, n = 136), HER2-positive (HER2+, n = 253), or triple-negative BC (TNBC, n = 149). Results In 37.4% of patients, new BM emerged at a median of 10.5 months after brain-directed treatment for initial BM. The 1-year actuarial rate of new BM for HR+/HER2-, HER2+, and TNBC were 51.9%, 44.0%, and 69.6%, respectively (p = 0.008). Initial whole-brain radiotherapy (WBRT) reduced new BM rates (22.5% reduction at 1 year, p < 0.001) according to molecular subtype (HR+/HER2-, 42% reduction at 1 year, p < 0.001; HER2+, 18.5%, p = 0.004; TNBC, 16.9%, p = 0.071). Multivariate analysis revealed an increased risk of new BM for the following factors: shorter intervals between primary BC diagnoses and BM (p = 0.031); TNBC (relative to HR+/HER2-) (p = 0.016); presence of extracranial metastases (p = 0.019); number of BM (>4) (p < 0.001); and BM in both tentorial regions (p = 0.045). Anti-HER2 therapy in HER2+ patients (p = 0.013) and initial use of WBRT (p < 0.001) significantly lowered new BM development. Conclusions Tumor molecular subtypes were associated with both rates of new BM development and the effectiveness of initial WBRT. Anti-HER2 therapy in HER2+ patients significantly lowered new BM occurrence.

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