The abnormal expression of cell surface receptors on tumor cells has become a major focus of efforts to individualize cancer therapy. Receptors involved in cell proliferation and programmed death are commonly targeted with antibody therapies, and new treatment modalities seek to exploit this abnormality to preferentially deliver toxic payloads to tumor cells. However, because of the complexity of tumor vasculature and leakage, the ability to noninvasively quantify the availability of these receptors remains elusive, precluding quantitative characterization and longitudinal monitoring of tumor receptor concentration. This project aims to advance a novel noninvasive MRI-coupled optical imaging approach that accounts for contrast agent pharmacokinetics and thus is capable of quantifying receptor concentration and availability in sub-surface tumors. This capability is enabled by imaging the kinetics of two fluorescent tracers injected simultaneously, one targeted to the receptor of interest, and the other to a non-targeted counterpart. Fitting the time course data to a dual-tracer compartmental model allows the recovery the density of cellular receptors available for binding. Accessing this parameter noninvasively could have a profound impact on drug development programs and even clinical practice, enabling characterization and tracking of drug targets in tumors.
The aims i n this project are designed to advance and validate all aspects of this technology. Specifically, a novel, low cost multispectral fluorescence tomography system dedicated to MRI-guided dual tracer fluorescence tomography (MRg-DTFT) in preclinical MRI research scanners will be developed, validated and used to explore the molecular response to new cancer therapies. Imaging performance of the instrument will be assessed using multi-tracer phantoms and by comparing in vivo animal images to co-registered fluorescence imaging of ex-vivo tissue slices. Significant development effort will also be directed towards optimizing the image processing and reconstruction algorithms required for fully integrated MRI-optical image recovery and analysis for the dual-tracer approach, with the ultimate aim of enabling one-click parameter recovery and visualization. These tools will be deployed to further validate the dual-tracer approach through extensive animal experiments which examine receptor density in multiple orthotopic glioblastoma tumors known to have varying receptor expression profiles and vascular structure. Finally, this unique capability will be deployed to investigate the effect an emerging tumor- penetrating therapeutic adjuvant has on available receptor density.

Public Health Relevance

Targeting the unique abnormalities of individual tumors is a major focus of current efforts towards personalized cancer therapy. The ability to directly assess these abnormalities using imaging technology would be a major advance for drug development programs and even clinical practice; however, this capability has remained elusive due to the abnormal and complex vascular structure in tumors. We are developing a novel imaging methodology that overcomes these barriers, and the proposed work aims to further advance this potentially enabling technology to establish the technique as a drug research standard and lay the groundwork for clinical deployment.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA184354-02
Application #
8828624
Study Section
Biomedical Imaging Technology Study Section (BMIT)
Program Officer
Zhang, Huiming
Project Start
2014-04-01
Project End
2019-02-28
Budget Start
2015-03-01
Budget End
2016-02-29
Support Year
2
Fiscal Year
2015
Total Cost
Indirect Cost
Name
Dartmouth College
Department
Engineering (All Types)
Type
Biomed Engr/Col Engr/Engr Sta
DUNS #
041027822
City
Hanover
State
NH
Country
United States
Zip Code
Sadeghipour, Negar; Davis, Scott C; Tichauer, Kenneth M (2018) Quantifying cancer cell receptors with paired-agent fluorescent imaging: a novel method to account for tissue optical property effects. Proc SPIE Int Soc Opt Eng 10497:
Sadeghipour, Negar; Davis, Scott C; Tichauer, Kenneth M (2018) Correcting for targeted and control agent signal differences in paired-agent molecular imaging of cancer cell-surface receptors. J Biomed Opt 23:1-11
Sadeghipour, N; Davis, S C; Tichauer, K M (2017) Generalized paired-agent kinetic model for in vivo quantification of cancer cell-surface receptors under receptor saturation conditions. Phys Med Biol 62:394-414
Davis, Scott C; Tichauer, Kenneth M (2016) Small-Animal Imaging Using Diffuse Fluorescence Tomography. Methods Mol Biol 1444:123-37
Elliott, Jonathan T; Samkoe, Kimberley S; Davis, Scott C et al. (2016) Image-derived arterial input function for quantitative fluorescence imaging of receptor-drug binding in vivo. J Biophotonics 9:282-95
Elliott, Jonathan T; Dsouza, Alisha V; Davis, Scott C et al. (2015) Review of fluorescence guided surgery visualization and overlay techniques. Biomed Opt Express 6:3765-82
Holt, Robert W; Demers, Jennifer-Lynn H; Sexton, Kristian J et al. (2015) Tomography of epidermal growth factor receptor binding to fluorescent Affibody in vivo studied with magnetic resonance guided fluorescence recovery in varying orthotopic glioma sizes. J Biomed Opt 20:26001