AI Article Synopsis
- The study aimed to assess how effective intravoxel incoherent motion (IVIM) diffusion-weighted imaging (DWI) is in measuring immune responses to chemotherapy in mouse tumor models and breast cancer patients.
- The research involved comparing tumor responses between treated and control groups of mice, with various imaging and pathology techniques used to track changes over time.
- Results indicated that the treated group had a smaller tumor volume and significant changes in immune cell markers, suggesting that IVIM DWI may be a useful tool for evaluating chemotherapy's impact on immune responses.
Article Abstract
Objective: To evaluate the predictive value of intravoxel incoherent motion (IVIM) diffusion-weighted imaging (DWI) in the quantitative assessment of conventional chemotherapy-activated immune responses in mouse tumor models and clinics.
Methods: A total of 19 subcutaneous tumor-bearing mice were randomly divided into treated and control groups. Both groups had orderly IVIM DWI examinations before and on days 6 and 12 after the administration of cyclophosphamide (CPA) or saline. Pathologic examinations were performed, including HE staining and immunohistochemistry (IHC). The expressions of immune-related genes in the tumor were measured by qPCR. In addition, six patients with breast cancer requiring neoadjuvant chemotherapy (NACT) also underwent functional MRI examinations and IHC to determine potential antitumor immune response.
Results: At the end of the study, the CPA treatment group showed the lowest tumor volume compared to the control group. For pathological examinations, the CPA treatment group showed a lower percentage of CD31 staining ( < 0.01) and Ki-67 staining (P<0.01), and a higher percentage of TUNEL staining ( < 0.01). The tumoral pseudodiffusion coefficient (D*) value showed a positive correlation with the CD31-positive staining rate ( = 0.729, 0.0001). The diffusion related parameters (D) value was positively correlated with TUNEL (r = 0.858, 0.0001) and negatively correlated with Ki-67 (r = -0.904, 0.0001). Moreover, a strong induction of the expression of the immune responses in the CPA treatment group was observed on day 12. D values showed a positive correlation with the Ifnb1-, CD8a-, Mx1-, Cxcl10- ( = 0.868, 0.864, 0.874, and 0.885, respectively, < 0.0001 for all). Additionally, the functional MRI parameters and IHC results in patients with breast cancer after NACT also showed a close correlation between D value and CD8a ( = 0.631, = 0.028).
Conclusions: The treatment response induced by immunogenic chemotherapy could be effectively evaluated using IVIM-DWI. The D values could be potential, sensitive imaging marker for identifying the antitumor immune response initiated by immunogenic chemotherapy.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136146 | PMC |
| http://dx.doi.org/10.3389/fonc.2022.796936 | DOI Listing |
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