Meeting Banner
Abstract #4540

Comparison of breast cancer subtypes in treatment response using Dynamic Contrast-Enhanced MRI

Sawwal Qayyum1, Jin Zhang1, Eric Aronowitz2, Myung Shin Han1, Seung Koo Lee1, and Gene Kim1
1Radiology, Weill Cornell Medical, New York City, NY, United States, 2Citigroup Biomedical Imaging Center, Weill Cornell Medical, New York City, NY, United States

Synopsis

Keywords: Biology, Models, Methods, Breast, Vascular, Image Reconstruction, Cancer

Motivation: Breast cancer molecular subtype may affect therapeutic efficacy of metronomic chemotherapy, which currently has not been investigated with non-invasive methods.

Goal(s): This study is to utilize DCE-MRI for quantitative measurement of treatment response in different breast cancer subtypes.

Approach: Preclinical orthotopic models 67NR(ER+) and 4T1(triple negative) of breast cancer were treated with the same metronomic chemotherapy, while the heterogenous treatment response was evaluated using DCE-MRI.

Results: In both tumor models, treatment induced higher Vp, Fp, and Ktrans. The 67NR tumors had higher vascular measures with slower growth rates than the 4T1 tumors.

Impact: The preliminary data in this study suggest that the tumor volume alone does not provide adequate information about the changes induced by treatment, and the treatment response differs substantially between breast cancer subtypes as observed by DCE-MRI parameters.

How to access this content:

For one year after publication, abstracts and videos are only open to registrants of this annual meeting. Registrants should use their existing login information. Non-registrant access can be purchased via the ISMRM E-Library.

After one year, current ISMRM & ISMRT members get free access to both the abstracts and videos. Non-members and non-registrants must purchase access via the ISMRM E-Library.

After two years, the meeting proceedings (abstracts) are opened to the public and require no login information. Videos remain behind password for access by members, registrants and E-Library customers.

Click here for more information on becoming a member.

Keywords