Project Funding Details


Title
Optimizing the Delivery of Intensity-Modulated Radiation Therapy to Lung Tumours Influenced by Respiratory Motion
Alt. Award Code
13979_1
Funding Organization
Ontario Institute for Cancer Research
Budget Dates
2010-04-01 to 2013-03-31
Principal Investigator
Gaede, Stewart ORCiD Logo 0000-0001-9941-4905
(ORCiD iD)
Institution
London Health Sciences Centre
Region
North America
Location
London, ON, CA

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Technical Abstract

Lay abstract (no permission to release technical abstract): There is conflicting evidence regarding the impact of motion on IMRT delivery. The interplay between moving tumours and moving multi-leaf collimators (MLC) can cause discrepancies between delivered and calculated dose. It appears through simplified models for fixed beam IMRT that this effect may average out over a course of treatment. However, technological advances has recently classified IMRT into three categories: 1) fixed beam IMRT; 2) tomotherapy; and 3) volumetric modulated arc therapy (VMAT). Fixed-beam IMRT holds the beam direction fixed while intensity-modulation is accomplished by changing the MLC shape during treatment. Tomotherapy is accomplished by moving the patient through a thin radiation beam that is constantly rotating around the patient. An MLC in which the 64 leaves are independently opened or closed modulate the beam. For VMAT, the MLC, the gantry rotation speed, and the dose rate are all changing during as a broad radiation beam is rotated around the patient who is lying on a fixed couch. We hypothesize that the dosimetric impact of respiratory motion will be significantly different for each delivery method. This study aims to investigate the dosimetric effects of moving lung tumours to each class of Intensity-Modulated Radiation Therapy (IMRT) delivery. We will combine the use of a commercially available phantom designed to verify arc-based IMRT with a respiratory motion platform capable moving the phantom similar to real-patient motion waveforms. IMRT plans of multiple patients of varying tumour size and motion will be generated for both simple sinusoidal motion with varying amplitude, and for multiple patients with realistic tumour motion detected by 4D-CT imaging. All measurements will be repeated 30 times to simulate a patient's full course of treatment. The measurements will be accumulated and compared to the calculated radiation dose. Action levels for each IMRT method will be determined. Next, we will investigate respiratory-gated radiotherapy, where the radiation beam only triggers at a certain predetermined phase of the breathing cycle, in hopes that it will reduce the dosimetric inaccuracies of free-breathing IMRT. Finally, we will develop a tool that will predict the best treatment method based on pre-treatment imaging. Once this pre-clinical study is complete, we will then implement an in-house clinical trial to investigate radiation dose escalation to moving lung tumours. This transition from benchtop to bedside fits the OICR mandate as translational research designed to improve the management of lung cancer.

Public Abstract

See Tech Abstract

Cancer Types

  • Lung Cancer

Common Scientific Outline (CSO) Research Areas

  • 5.2 Treatment Localized Therapies - Clinical Applications