ISMRM & ISMRT Annual Meeting & Exhibition • 10-15 May 2025 • Honolulu, Hawai'i

ISMRM & ISMRT 2025 Annual Meeting & Exhibition

Digital Poster

Preclinical Cancer: Body

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Preclinical Cancer: Body
Digital Poster
Preclinical
Monday, 12 May 2025
Exhibition Hall
14:45 -  15:45
Session Number: D-211
No CME/CE Credit

 
Computer Number: 129
1944. Multimodal imaging of tumor metabolism and microenvironment in feline sarcoma patients using hyperpolarized 13C MRI and PET
M. Grashei, T. Groll, S. Kahl, S. Baer, E. Bliemsrieder, F. van Heijster, A. Wendlinger, P. Wodtke, J. Cabello, S. Notohamiprodjo, C. Lohrmann, M. Schwaiger, W. Weber, K. Steiger, A. Meyer-Lindenberg, J. Hirschberger, C. Baumgartner, F. Schilling
Department of Nuclear Medicine, TUM University Hospital, Munich, Germany
Impact: Hyperpolarized 13C MRI allows sarcoma subtype and grade differentiation in cat patients in contrast to [18F]FMISO-PET and DWI. Acidification outperforms all other parameters as biomarker for cat patient prognosis, rendering hyperpolarized pH imaging a promising technique for clinical translation.
 
Computer Number: 130
1945. Correlation between MRI parameters and atrophy biomarkers of muscle in a preclinical model of pancreatic cancer
D. Lee, R. Vohra, Y-N Wang, S. Totten, H. Son, H. Kerr, M. Campbell, D. Marcinek, J. Garcia
University of Washington, Seattle, United States
Impact: MR measures offer the potential to evaluate skeletal muscle fiber atrophy in preclinical models of pancreatic ductal adenocarcinoma and more impotantly these results can be translated to patients with cancer cachexia
 
Computer Number: 131
1946. Quantitative MRI Oximetry: Combining EPR and OE-MRI for Volumetric Mapping of Hypoxia in Tumors
C. Ubert, V. Kassey, M. Kmiec, P. Kuppusamy
Dartmouth College, Hanover, United States
Impact: This study investigates a calibration method, which could act as a quality assessment tool for the hypoxia maps generated using OE-MRI, potentially improving personalized cancer treatments.
 
Computer Number: 132
1947. Metabolic and Functional Imaging Biomarkers of Response to Immunotherapy in Melanoma
P. K. Gupta, S. Orlovskiy, F. Arias-Mendoza, S. Nova, D. Nelson, S. Pickup, M. Farwell, K. Nath
Perelman School of Medicine, University of Pennsylvania, Philadelphia, United States
Impact: This study emphasizes the potential of early subcellular changes (metabolism, pH, bioenergetics, diffusion, T2 relaxation) as predictive biomarkers of melanoma immunotherapy response. Preliminary findings with metabolic modulators indicate possible strategies for enhancing treatment outcomes through metabolic modulation.
 
Computer Number: 133
1948. Early Monitoring of Immunotherapy Efficacy in Triple-Negative Breast Cancer by Granzyme B-Responsive MR/NIR Fluorescence Imaging
D. Yao, Y. Chen, D. Wang
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
Impact: Early prediction of the efficacy of immunotherapy is of great significance for optimizing the treatment plan in time and avoiding overtreatment of patients with low response.
 
Computer Number: 134
1949. Magnetic Resonance Molecular Imaging of Patient-Derived Xenografts with MT218
R. Hall, Z-R Lu
Case Western Reserve University, Cleveland, United States
Impact: We demonstrate that MT218 can effectively enhance patient-derived xenograft tumors of triple negative breast cancer, a clinically relevant tumor model, further supporting the clinical translation of MT218 for magnetic resonance molecular imaging of cancer.
 
Computer Number: 135
1950. In vitro Hyperpolarized 13C-Pyruvate NMR Spectroscopy for the Assessment of Treatment Response in Different Hepatocellular Carcinoma Subtypes
Q. Dou, S. Mirrione, K. Dos Santos, Y-F Yen, L. Tsai
Athinoula A. Martinos Center for Biomedical Imaging, Harvard Medical School, Charlestown, United States
Impact: Cancer cells undergo extensive metabolic reprogramming to support rapid proliferation, survival, and treatment resistance. 13C NMR spectroscopy can rapidly provide valuable insight into cellular metabolism and therapeutic efficacy, potentially enabling clinicians to provide more personalized cancer care.
 
Computer Number: 136
1951. Metabolic Biomarkers of Therapeutic Response in YUMM1.7 Melanoma Targeting BRAF and MEK Inhibition
P. K. Gupta, L. Li, S. Nova, S. Orlovskiy, D. Nelson, F. Arias-Mendoza, M. Farwell, K. Nath
Perelman School of Medicine, University of Pennsylvania, Philadelphia, United States
Impact: This study shows that combining dabrafenib and trametinib may block the overactive BRAF and MEK proteins. Variations in critical metabolites (lactate and alanine), bioenergetics, NADH, and pH may explain differential therapeutic responses in YUMM1.7 melanoma models.
 
Computer Number: 137
1952. Quantitative DCE MRI of vascular perfusion in preclinical breast cancer:Comparative analysis of LRRM and Tofts models
C. Dhakan, A. Khaled, C. Macaskill, J. De La Cerda, F. W. Schuler, C. Flask, M. Pagel
MD Anderson Cancer Center, Houston, United States
Impact: These findings demonstrate the effectiveness of the LRRM for evaluating DCE MRI  when monitoring vascular changes induced by VDAs in tumors. Future studies may explore the use of LRRM for DCE MRI to evaluate other anti-cancer treatments.
 
Computer Number: 138
1953. Metabolotheranostics of metabolites identified by 1H MRS achieved by targeting major metabolic transporters with photoimmunotherapy
P. Khandelwal, J. Jin, R. K. Sharma, J. D. Barnett, M-F Penet, Y. Mironchik, B. Krishnamachary, H. Kobayashi, Z. M. Bhujwalla
Johns Hopkins University, Baltimore, United States
Impact: Since choline, glutamine, and glucose are dysregulated in most cancers, our studies can significantly expand the scope of targeted cancer treatments that do not express cell surface targets for antibody-drug conjugates or radiotheranostics for systemic therapies. 
 
Computer Number: 139
1954. Development of a Scoring System for Predicting the Benign-Malignant Degree of IPNB Based on Imaging Features and Clinical Indicators
J. Chu, Y. Zhao, W. Xiao, Z. Zhang, J. Zhang, L. Han
The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China
Impact: The scoring system demonstrates high sensitivity and specificity in predicting IPNB malignancy. This scoring system, based on clinical data and imaging features, enables early IPNB screening and surgical planning.
 
Computer Number: 140
1955. Resting-state fMRI analyses of a pain state transition induced by a chemokine signal-regulating agent in tumor model mice
S. Yoshinaga, T. Shinjo, Y. Kawachi, Y. Terashima, E. Toda, K. Matsushima, T. Tsurugizawa, H. Terasawa
Kumamoto University, Kumamoto, Japan
Impact: The pain state transition induced by the analgesic agent in the tumor-bearing mouse brain was characterized by resting-state fMRI. Our experimental system is useful for the evaluation of new analgesic candidates in nonclinical and, expectantly, clinical studies.
 
Computer Number: 141
1956. 19F MRI To Monitor Cancer Progression Post-immunotherapy and Radiation Therapy
E. Qi, H. Yang, B. Howerton, F. Chapelin
UC San Diego, San Diego, United States
Impact: 19F MRI enables noninvasive monitoring of macrophage dynamics during radiation therapy and immunotherapy treatments, as well as anticipate tumor growth. This approach will be invaluable for future research on the role of inflammation in tumor response to therapy and recurrence. 
 
Computer Number: 142
1957. Spatial biomechanics quantification of the Tumoural MicroEnvironment of a HepG2 spheroids with Magnetic Resonance Elastography
M. Ducamp, A-S Van Schelt, V. Paradis, A. Hammoutene, L. Aguilera Munoz, A. Beaufrere, A. Boumaza, G. Mangin, M. Parsons, R. Sinkus
King's College London, London, United Kingdom
Impact: Developing 3D culture model, starting from patient’s biopsy samples, that is predictive to their in vivo response to treatment, easily applicable could be relevant in the field of tailored medicine. This could spare the patient non-effective chemotherapy exposure or surgery.
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