Abstract
Objectives
The aim of this study is to investigate the correlation of survival outcomes with imaging biomarkers from multiparametric magnetic resonance imaging (MRI) in patients with brain metastases from breast cancer (BMBC).
Methods
This study was approved by the institutional review board. Twenty-two patients with BMBC who underwent treatment involving bevacizumab on day 1, etoposide on days 2-4, and cisplatin on day 2 in 21-day cycles were prospectively enrolled for a phase II study. Three brain MRIs were performed: before the treatment, on day 1, and on day 21. Eight imaging biomarkers were derived from dynamic contrast-enhanced MRI (Peak, IAUC60, Ktrans, kep, ve), diffusion-weighted imaging [apparent diffusion coefficient (ADC)], and MR spectroscopy (choline/N-acetylaspartate and choline/creatine ratios). The relative changes (Δ) in these biomarkers were correlated with the central nervous system (CNS)-specific progression-free survival (PFS) and overall survival (OS) using the Kaplan-Meier and Cox proportional hazard models.
Results
There were no significant differences in the survival outcomes as per the changes in the biomarkers on day 1. On day 21, those with a low ΔKtrans (p = 0.024) or ΔADC (p = 0.053) reduction had shorter CNS-specific PFS; further, those with a low ΔPeak (p = 0.012) or ΔIAUC60 (p = 0.04) reduction had shorter OS compared with those with high reductions. In multivariate analyses, ΔKtrans and ΔPeak were independent prognostic factors for CNS-specific PFS and OS, respectively, after controlling for age, size, hormone receptors, and performance status.
Conclusions
Multiparametric MRI may help predict the survival outcomes in patients with BMBC.
Key Points
• Decreased angiogenesis after chemotherapy on day 21 indicated good survival outcome.
• ΔK trans was an independent prognostic factors for CNS-specific PFS.
• ΔPeak was an independent prognostic factors for OS.
• Multiparametric MRI helps clinicians to assess patients with BMBC.
• High-risk patients may benefit from more intensive follow-up or treatment strategies.
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Abbreviations
- 1H-MRS:
-
Proton magnetic resonance spectroscopy
- ADC:
-
Apparent diffusion coefficient
- Cho:
-
Choline
- CNS:
-
Central nerve system
- Cre:
-
Creatine
- DCE-MRI:
-
Dynamic contrast-enhanced magnetic resonance imaging
- DWI:
-
Diffusion-weighted imaging
- ECOG:
-
Eastern Cooperative Oncology Group
- ER:
-
Estrogen receptor
- HER2:
-
Human epidermal growth factor receptor 2
- IAUC60 :
-
Initial area under curve for the first 60 s
- k ep :
-
Reflux constant
- K trans :
-
Volume transfer constant
- NAA:
-
N-acetylaspartate
- OS:
-
Overall survival
- Peak:
-
(maximal signal – baseline signal)/baseline signal
- PFS:
-
Progression-free survival
- PR:
-
Progesterone receptor
- ROI:
-
Region of interest
- v e :
-
Extravascular extracellular volume fraction
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Funding
This study has received funding by the National Taiwan University (NTU-ICRP-103R7557 to Y.S.L.), Ministry of Science and Technology, Taiwan (MOST 103-2314-B-002-170-MY3 to Y.S.L.)
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The scientific guarantor of this publication is Tiffany Ting-Fang Shih.
Conflict of interest
The authors of this manuscript declare no relationships with any companies, whose products or services may be related to the subject matter of the article.
Statistics and biometry
Fu-Chang Hu, Sc.D., kindly provided statistical advice for this manuscript.
Informed consent
Written informed consent was obtained from all subjects (patients) in this study
Ethical approval
Institutional Review Board approval was obtained.
Study subjects or cohorts overlap
All study subjects or cohorts have been previously reported.
This study is based on our previous works (Clin Cancer Res. 2015 Apr 15;21(8):1851-8; BMC Cancer. 2016 Jul 13;16:466. NCT01281696).
Methodology
• prospective
• diagnostic or prognostic study
• performed at one institution
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Chen, BB., Lu, YS., Yu, CW. et al. Imaging biomarkers from multiparametric magnetic resonance imaging are associated with survival outcomes in patients with brain metastases from breast cancer. Eur Radiol 28, 4860–4870 (2018). https://doi.org/10.1007/s00330-018-5448-5
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DOI: https://doi.org/10.1007/s00330-018-5448-5