Conventional magnetic resonance imaging has good sensitivity for detecting very early breast cancers, andmay be a valuable for screening women who are at high risk for breast cancer. However, its specificity isinadequate, particularly given its high sensitivity. As a result there is a concern that MRI scans lead tounnecessary treatment. We propose to significantly increase sensitivity and specificity with improvedspectral, temporal and spatial sampling (MRITSS). MRITSS has two components. High spectral and spatialresolution MRI provides a high resolution water spectrum associated with each image voxel, and the waterspectral lineshape is analyzed to produce improved anatomic and functional MR images. High temporal andspatial resolution imaging during contrast media uptake and washout allows accurate measurement ofperfusion and other physiologic parameters. We will test the hypothesis that the combination of these twoapproaches - MRITSS - improves specificity and sensitivity in the high risk population that would benefitmost from MRI. We will study 'incidental' lesions that are found during clinical MRI screening, since theselesions are most susceptible to incorrect diagnosis. An additional research scan before biopsy will acquiredata from an 'incidental lesion', using MRITSS. Conventional and MRITSS data will be evaluated usingstandard morphologic and functional parameters to arrive at a diagnosis. We will determine whetherMRITSS increases specificity and sensitivity, using the pathologist's diagnosis as the gold standard. Inaddition, we will determine whether MRI parameters are correlated with genetic and biologic markers forcancer risk, including microvessel density, cell proliferation markers, VEGF receptors, and P53, HER2,BRCA1 and BRCA2. The study will include African American women who are at particularly high risk foraggressive early breast cancer. We will compare the MRI parameters for breast lesions in these women withthose for the other women in the study.The research will have a significant impact on clinical managements of breast cancer. If the resultsdemonstrate that MRITSS has high specificity for early breast cancer- this will support increased clinicaluse of MRI for screening high risk women, and integration of improved spectral, spatial, and temporalsampling into clinical MRI. In addition, the research provides an unusual opportunity to correlate MRIparameters with biological markers for malignancy in early breast cancers. This could lead to improveddesign of MRI protocols and interpretation of MR images. The research is an interdisciplinary collaborationbetween Radiologists, Oncologists, Surgeons, Pathologists, Medical Physicists, and Statisticians with strongtrack records in breast imaging and breast cancer treatment.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center (P50)
Project #
1P50CA125183-01
Application #
7198291
Study Section
Special Emphasis Panel (ZCA1-GRB-I (O1))
Project Start
2006-11-01
Project End
2011-07-31
Budget Start
2006-11-01
Budget End
2007-07-31
Support Year
1
Fiscal Year
2006
Total Cost
$186,816
Indirect Cost
Name
University of Chicago
Department
Type
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Guindalini, Rodrigo Santa; Zheng, Yonglan; Abe, Hiroyuki et al. (2018) Intensive surveillance with bi-annual dynamic contrast-enhanced magnetic resonance imaging downstages breast cancer in BRCA1 mutation carriers. Clin Cancer Res :
Rebbeck, Timothy R (see original citation for additional authors) (2018) Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. Hum Mutat 39:593-620
Zheng, Yonglan; Walsh, Tom; Gulsuner, Suleyman et al. (2018) Inherited Breast Cancer in Nigerian Women. J Clin Oncol 36:2820-2825
Wang, Shengfeng; Ogundiran, Temidayo; Ademola, Adeyinka et al. (2018) Development of a Breast Cancer Risk Prediction Model for Women in Nigeria. Cancer Epidemiol Biomarkers Prev 27:636-643
Debiasi, Márcio; Polanczyk, Carisi A; Ziegelmann, Patrícia et al. (2018) Efficacy of Anti-HER2 Agents in Combination With Adjuvant or Neoadjuvant Chemotherapy for Early and Locally Advanced HER2-Positive Breast Cancer Patients: A Network Meta-Analysis. Front Oncol 8:156
Feng, Ye; Rhie, Suhn Kyong; Huo, Dezheng et al. (2017) Characterizing Genetic Susceptibility to Breast Cancer in Women of African Ancestry. Cancer Epidemiol Biomarkers Prev 26:1016-1026
Hamdi, Yosr; Soucy, Penny; Kuchenbaeker, Karoline B et al. (2017) Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3. Breast Cancer Res Treat 161:117-134
Michailidou, Kyriaki (see original citation for additional authors) (2017) Association analysis identifies 65 new breast cancer risk loci. Nature 551:92-94
Rudin, Shoshana; Marable, Marcus; Huang, R Stephanie (2017) The Promise of Pharmacogenomics in Reducing Toxicity During Acute Lymphoblastic Leukemia Maintenance Treatment. Genomics Proteomics Bioinformatics 15:82-93
Geeleher, Paul; Huang, R Stephanie (2017) Exploring the Link between the Germline and Somatic Genome in Cancer. Cancer Discov 7:354-355

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