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Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- WILD DOG PHYSICS, LLC
- Proposal award date
- 2021-04-01
- Contract end date
- 2023-06-30
- UEI
- L8D1CH5FK9X3
- Solicitation number
- PAR22-073
- Topic code
- NCI
Research abstract
Executive SummaryRadiation Therapy is an effective component of the treatment strategy for patients suffering from
cancer. Advanced techniques such as intensity modulated radiation therapy (IMRT), image-guided RT (IGRT),
stereotactic body RT (SBRT) and stereotactic radiosurgery (SRS) improve outcomes and are delivered using
medical linear accelerators (i.e., ‘linacs”). SBRT is especially appealing given that the precise treatments are
delivered in 1-5 daily treatment fractions, as opposed to the 20-40 fractions required for conventional
techniques. Providing SBRT in rural settings can improve access by administering these precise, abbreviated
treatments to patients who have difficulty traveling to large, regional medical centers. Further, adoption of
automated techniques for quality control and enhanced tele-dosimetry can support peer review, improve
quality, reduce dependence on (local) expertise and reduce operating costs.The quality assurance (QA) that medical physicists provide is critical for safe treatments, yet there is a
shortage of qualified medical physicists (QMPs), both in the US and globally. At the same time, more centers
are introducing modern techniques that are more precise but intrinsically have more risk, due the high doses
and geometric precision required. There is widespread noncompliance with industry standard QA protocols in
the US and internationally. Existing QA devices have not evolved sufficiently to provide the precision, versatility
and efficiency that is needed for high precision RT. Given these exacerbated safety risks, the market needs a
paradigm shift in how QA is performed in modern RT.Wild Dog Physics (WDP) proposes to design and test a new-generation QA device that addresses these
unmet medical needs. When complete, it will be more precise, efficient, and comprehensive than any QA
solution currently on the market. The proposed project seeks to develop a clinical prototype to be tested in the
Radiation Therapy clinic at the University of Kentucky, as well as regional partner organizations located in
rural, underserved areas. The prototype will be developed using the following milestones: Design and build i)
a novel, a small-form-factor optical tunnel (SFFOT), ii) a laminated side wall with a scintillating phosphor
screen and ‘switchable film’ outer layer to facilitate ambient light rejection and iii), a hybrid beam quality /
compact CT phantom. The project will culminate with the construction of an integrated prototype that will be
tested for technical and clinical performance.Towards this end, the specific aims of this project are:
Specific Aim 1: Build and test the 3 primary subcomponents of an integrated device; a) a SFFOT that can
collect an image(s) of the entire useful interior surface, transmit the image(s) to an electronic camera sensor
through a small form-factor (lt 5 cm diameter) passive optical chain; b) a laminated side wall consisting of an
outer, electronically polarizing optical layer, and an inner radio-luminescent layer, and c) a hybrid ‘dose
phantom’ to be integrated onto one side of the device which will serve as a tissue-equivalent phantom so that
beam quality metrics can be monitored and to host CT image quality test objects.
Specific Aim 2: Construct and test a clinical prototype; The system’s ability to monitor machine performance in
a clinical setting will be validated. Sensitivity to detecting changes in relative and absolute radiation output, as
well as field edge positioning will be measured, with success criteria defined as 0.5% and 0.5 mm. Data
acquisition time for monthly QA tests will be measured and success defined as less than 30 minutes.The consolidation of multiple device functions combined with the ease of use and measurement
precision enable a paradigm shift in how medical physics services and quality assurance are rendered. Sparse
but efficient daily QA protocols will be replaced with comprehensive data collection and automated analysis, at
no additional cost in time or staffing. High precision radiation treatments can be safely brought to rural and
underserved areas, with safety, efficiency and precision improved in any center using the innovation.To date, we have established the feasibility of constructing a single device that can acquire
comprehensive QA metrics in less than 60 minutes. Presently, all subsystems have been tested and found to
perform as required. A three-dimensional prototype has been built and is being validated by our clinical
partner at the UK Radiation Medicine department. WDP is in the process of seeking SBIR Phase 2 funding to
further develop the technology to the point of commercialization.
Technology keywords
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Other awards by this recipient
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Research funding history
2 SBIR/STTR records share this UEI (2021–2024). Reported award amounts total $2,449,089. Reported amounts are not federal obligations.
Phases: Phase II, Phase I
Agencies: Department of Health and Human Services
Agency intelligence
Department of Health and Human Services
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