The fundamental goal of this work is to improve our ability to optimize the overall plan for each patient'streatment course ('comprehensive' treatment course optimization). Current planning methods make use ofonly a static single instance of the patient's anatomy (typically a treatment planning CT scan), and create anoptimized treatment plan based on the clinical therapy prescription, using interactive or inverse planningoptimization techniques (for Intensity Modulated Radiation Therapy (IMRT)). However, our knowledge ofthe patient and treatment goals is not static, but dynamic. Throughout the patient's course of treatment, weobtain new information on geometrical localization, inter- and intra-fraction motion, clinical response, andthe precision to which we can predict uncertainties in the data used for planning. To better account for andutiltize this knowledge, the proposed research will develop and evaluate new paradigms for comprehensiveoptimization of the entire treatment course, evaluating potential improvements over the single-instanceplanning/optimization techniques which are widely used throughout the radiotherapy community. Theproject will develop a planning/optimization framework for individualized optimization which incorporatesgeometric, dosimetric, clinical and biological information as it becomes available (Aim 1), studyimprovements in single-stage optimization procedures for the multi-criteria problems encountered intherapy planning (Aim 2), and explicitly investigate multi-stage optimization methods for planning anddelivery of the entire treatment course (Aim 3). This project will show that development of plan optimizationstrategies which 1) explicitly account for setup uncertainty and/or organ motion, 2) make use of updatedclinical, biological, dosimetric and geometric information to refine the plan, and 3) model and optimizemulti-stage adaptive therapy for the entire treatment course will better tailor the overall treatment plan toeach individual patient and predict improvements over the current static inverse plan generated once foreach patient.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA059827-11A1
Application #
7082531
Study Section
Subcommittee G - Education (NCI)
Project Start
2006-04-01
Project End
2011-06-30
Budget Start
2006-04-01
Budget End
2007-06-30
Support Year
11
Fiscal Year
2006
Total Cost
$259,334
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
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Kong, Feng-Ming Spring; Li, Ling; Wang, Weili et al. (2018) Greater reduction in mid-treatment FDG-PET volume may be associated with worse survival in non-small cell lung cancer. Radiother Oncol :
Shilkrut, Mark; Sapir, Eli; Hanasoge, Sheela et al. (2018) Phase I Trial of Dose-escalated Whole Liver Irradiation With Hepatic Arterial Fluorodeoxyuridine/Leucovorin and Streptozotocin Followed by Fluorodeoxyuridine/Leucovorin and Chemoembolization for Patients With Neuroendocrine Hepatic Metastases. Am J Clin Oncol 41:326-331
Jackson, William C; Tao, Yebin; Mendiratta-Lala, Mishal et al. (2018) Comparison of Stereotactic Body Radiation Therapy and Radiofrequency Ablation in the Treatment of Intrahepatic Metastases. Int J Radiat Oncol Biol Phys 100:950-958
Miften, Moyed; Vinogradskiy, Yevgeniy; Moiseenko, Vitali et al. (2018) Radiation Dose-Volume Effects for Liver SBRT. Int J Radiat Oncol Biol Phys :

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