Evaluation of metronomic chemotherapy response using diffusion and dynamic contrast-enhanced MRI.

TitleEvaluation of metronomic chemotherapy response using diffusion and dynamic contrast-enhanced MRI.
Publication TypeJournal Article
Year of Publication2020
AuthorsBaboli M, Winters KV, Freed M, Zhang J, Kim SGene
JournalPLoS One
Volume15
Issue11
Paginatione0241916
Date Published2020
ISSN1932-6203
KeywordsAdministration, Metronomic, Animals, Antimetabolites, Antineoplastic, Case-Control Studies, Contrast Media, Diffusion Magnetic Resonance Imaging, Feasibility Studies, Female, Fluorouracil, Longitudinal Studies, Magnetic Resonance Imaging, Mammary Neoplasms, Animal, Mice, Mice, Inbred BALB C, Neoplasm Metastasis, Treatment Outcome
Abstract

PURPOSE: To investigate the feasibility of using diffusion MRI (dMRI) and dynamic contrast-enhanced (DCE) MRI to evaluate the treatment response of metronomic chemotherapy (MCT) in the 4T1 mammary tumor model of locally advanced breast cancer.

METHODS: Twelve Balb/c mice with metastatic breast cancer were divided into treated and untreated (control) groups. The treated group (n = 6) received five treatments of anti-metabolite agent 5-Fluorouracil (5FU) in the span of two weeks. dMRI and DCE-MRI were acquired for both treated and control groups before and after MCT. Immunohistochemically staining and measurements were performed after the post-MRI measurements for comparison.

RESULTS: The control mice had significantly (p<0.005) larger tumors than the MCT treated mice. The DCE-MRI analysis showed a decrease in contrast enhancement for the control group, whereas the MCT mice had a more stable enhancement between the pre-chemo and post-chemo time points. This confirms the antiangiogenic effects of 5FU treatment. Comparing amplitude of enhancement revealed a significantly (p<0.05) higher enhancement in the MCT tumors than in the controls. Moreover, the MCT uptake rate was significantly (p<0.001) slower than the controls. dMRI analysis showed the MCT ADC values were significantly larger than the control group at the post-scan time point.

CONCLUSION: dMRI and DCE-MRI can be used as potential biomarkers for assessing the treatment response of MCT. The MRI and pathology observations suggested that in addition to the cytotoxic effect of cell kills, the MCT with a cytotoxic drug, 5FU, induced changes in the tumor vasculature similar to the anti-angiogenic effect.

DOI10.1371/journal.pone.0241916
Alternate JournalPLoS One
PubMed ID33237905
PubMed Central IDPMC7688103
Grant ListP41 EB017183 / EB / NIBIB NIH HHS / United States
R01 CA160620 / CA / NCI NIH HHS / United States
R01 CA219964 / CA / NCI NIH HHS / United States
UG3 CA228699 / CA / NCI NIH HHS / United States
Related Institute: 
MRI Research Institute (MRIRI)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065