Approximately two thirds of patients with intrahepatic cancer present with unresectable disease. Our previous studies show that high dose conformal radiation combined with chemotherapy appears to prolong the survival of patients with unresectable intrahepatic cancers. However, attempts to increase radiation dose still further have been limited by the development of radiation-induced liver disease (RILD). The pathology of RILD is veno-occlusive disease, which is characterized by thrombosis within the central veins of the liver producing """"""""post"""""""" hepatic congestion. In the past, efforts to develop models to estimate the likelihood of developing RILD have been based primarily on the planned radiation dose distribution for the normal liver. These analyses have demonstrated that increasing mean liver dose correlates with the likelihood of developing RILD. While these models have permitted the safe delivery of far higher doses of radiation than have previously been possible, they also suggest that there is a broad range of individual patient sensitivity that is not reflected by predictions made solely based on the physical dose distribution or general clinical features. As the basic pathophysiology of RILD is venous occlusion, we develop the hypothesis that early monitoring of portal venous perfusion and hepatobiliary function would have the potential to predict liver function after irradiation, thereby permitting to safely deliver the higher dose to the tumor without an increase of complications. Our preliminary data provide evidence to support this hypothesis. In this R01 application, we propose to develop a model to predict liver function after the completion of radiation therapy based upon the radiation treatment plan, and the values of portal venous perfusion and hepatobiliary function assessed by DCE MRI and SPECT prior to and during radiation therapy. Also, we assess individual and regional radiation sensitivity during radiation therapy using the liver dose response function that we have developed, for prediction of liver function after irradiation. Our proposed approach is highly innovative and represents a new paradigm to investigate radiation toxicity in the liver. It has potential to be a tool for individualized therapy.

Public Health Relevance

Our previous studies show that high dose conformal radiation combined with chemotherapy appears to prolong the survival of patients with unresectable intrahepatic cancers. However, attempts to increase radiation dose still further have been limited by radiation-induced liver injury. Our long term goal is to develop a new imaging approach for prediction of radiation-induced syptomatic liver injury. Therefore, higher dose of radiation can be safely delivered to tumor in patients who can be better tolerant to radiation, thereby improving survival.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA132834-02
Application #
8119762
Study Section
Radiation Therapeutics and Biology Study Section (RTB)
Program Officer
Vikram, Bhadrasain
Project Start
2010-08-01
Project End
2015-05-31
Budget Start
2011-07-21
Budget End
2012-05-31
Support Year
2
Fiscal Year
2011
Total Cost
$342,014
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Simeth, Josiah; Johansson, Adam; Owen, Dawn et al. (2018) Quantification of liver function by linearization of a two-compartment model of gadoxetic acid uptake using dynamic contrast-enhanced magnetic resonance imaging. NMR Biomed 31:e3913
El Naqa, Issam; Johansson, Adam; Owen, Dawn et al. (2018) Modeling of Normal Tissue Complications Using Imaging and Biomarkers After Radiation Therapy for Hepatocellular Carcinoma. Int J Radiat Oncol Biol Phys 100:335-343
Johansson, Adam; Balter, James; Cao, Yue (2018) Rigid-body motion correction of the liver in image reconstruction for golden-angle stack-of-stars DCE MRI. Magn Reson Med 79:1345-1353
Matakos, Antonis; Balter, James M; Cao, Yue (2017) A Robust Method for Estimating B0 Inhomogeneity Field in the Liver by Mitigating Fat Signals and Phase-Wrapping. Tomography 3:79-88
Wang, Hesheng; Feng, Mary; Jackson, Andrew et al. (2016) Local and Global Function Model of the Liver. Int J Radiat Oncol Biol Phys 94:181-188
Johansson, Adam; Balter, James; Feng, Mary et al. (2016) An Overdetermined System of Transform Equations in Support of Robust DCE-MRI Registration With Outlier Rejection. Tomography 2:188-196
Wu, Victor W; Epelman, Marina A; Wang, Hesheng et al. (2016) Optimizing global liver function in radiation therapy treatment planning. Phys Med Biol 61:6465-84
Wang, Hesheng; Farjam, Reza; Feng, Mary et al. (2014) Arterial perfusion imaging-defined subvolume of intrahepatic cancer. Int J Radiat Oncol Biol Phys 89:167-74
Tsien, Christina; Cao, Yue; Chenevert, Thomas (2014) Clinical applications for diffusion magnetic resonance imaging in radiotherapy. Semin Radiat Oncol 24:218-26
Stenmark, Matthew H; Cao, Yue; Wang, Hesheng et al. (2014) Estimating functional liver reserve following hepatic irradiation: adaptive normal tissue response models. Radiother Oncol 111:418-23

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