Among the various IMRT techniques that have been proposed or implemented, IMAT, or intensity-modulated arc therapy, is one of the most promising approaches for achieving superior dose conformity with a minimized treatment time. However, due to the many degrees of freedom in IMAT planning, optimizing an IMAT plan is computationally difficult, and an effective method for IMAT planning is not yet available. Moreover, methods for IMAT (and other rotational delivery schemes) to handle breathing induced target motion are also lacking. The goal of this proposal is to develop a clinically practical IMAT planning system that allows tumor tracking and image guidance through a bioengineering research partnership (NIH PAR-04- 023). We hypothesize that by using advanced graph algorithmic techniques in computer science, we can develop a robust and effective IMAT planning software for both static and moving targets. A breathing synchronized delivery technique will ensure optimal treatment for all breathing phases in a breathing cycle.
The specific aims of this proposal are:
Specific Aim I : To assess the advantages and disadvantages of IMAT over other IMRT methods using the current IMAT planning tool, and to integrate our Monte-Carlo based dose calculation engine with IMAT planning.
Specific Aim II : To develop a 4D IMAT planning system and a breathing synchronized delivery mechanism under image guidance.
Specific Aim III : Verify clinical feasibility of the planning and delivery scheme developed in Aim II using a 4D phantom to ensure that the IMAT plans with breathing motion compensation can be delivered accurately using motion synchronized IMAT delivery scheme. We believe that the full use of 4D CT images to make a plan that ensures optimality at all breathing phases is a significant advancement of the existing art of radiotherapy. Successful achievement of the aforementioned project aims will provide planning and practical image guidance for the safe and efficient delivery of IMAT, and significantly improve cancer treatments. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
1R01CA117997-01A2
Application #
7236449
Study Section
Special Emphasis Panel (ZRG1-SBIB-Q (50))
Program Officer
Deye, James
Project Start
2007-06-01
Project End
2011-04-30
Budget Start
2007-06-01
Budget End
2008-05-31
Support Year
1
Fiscal Year
2007
Total Cost
$321,246
Indirect Cost
Name
University of Maryland Baltimore
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
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