Grant: Idea to Innovation
Queen's University
$152,990.00
Intraoperative calibration (iCAL) fro prostate brachytherapy
FY 2011-12
Summary
Prostate cancer is the second most common cancer in North American men. Brachytherapy, applied in about 55,000 cases annually in North America, entails the permanent implantation of radioactive sources into the prostate, under real-time ultrasound image guidance. Although brachytherapy has resulted in an improved prognosis, radiation toxicity remains a significant challenge. Brachytherapy systems require careful calibration to ensure the correct spatial relationship between the implant needles and the ultrasound image. Incorrect calibration leads to faulty delivery of the radiation dose, reducing the efficacy of cancer control and directly contributing to negative side effects like rectal ulcers and incontinence.
Calibration today is a costly, laborious and manual process, involving a great deal of subjective judgment by the operator. It is performed periodically, outside the operating room, with the assumption that calibration parameters remain valid over time. In reality, however, calibration parameters change during storage, transportation and setup of the equipment. Calibration errors are virtually impossible to detect during the procedure so the surgeon can never be certain whether the system is functioning correctly.
To improve contemporary practice, we calibrate the system in the operating room while the patient is being prepared for surgery. Our method is fast, fully automated and based on computations alone, eliminating subjectivity and human error. From our research in NSERC I2I Phase-I, we demonstrated the concept and prototype. Under the Phase-IIb grant, we will create a fully functional brachytherapy calibration system, field test it and bring it to readiness for commercial distribution. The resulting product will simultaneously reduce treatment costs, increase safety and improve the accuracy of prostate cancer brachytherapy.
The commercial partner for this proposal is Precision Therapeutics Inc. (PTI), a medical device company based in Kingston, Ontario. PTI develops ultrasound image guided systems for the diagnosis and treatment of prostate cancer. Through established strategic alliances, PTI has direct access to the prostate brachytherapy market in North America and worldwide.
Program
Idea to Innovation
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
396253-2010
Name nom
Fichtinger, Gabor
Department département
Computing, School of
Organization id
29
Institution établissement
Queen's University
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2011
Competition year année de concours
2010
Award amount
152990
Program id
I2IPJ
Program nane en
Idea to Innovation
Program name fr
De l'idée à l'innovation
Group en
Research partnerships programs
Group fr
Programmes de partenariat
Committee code
96
Committee name en
RPP Internal Decision Cttee
Committee name fr
Cté de décision interne - PPR
Area of application code
518
Area of application group en
Manufacturing processes and products
Area of application group fr
Procédés et produits industriels
Area of application en
Medical equipment and apparatus
Area of application fr
Appareils et instruments médicaux
Research subject code
1900
Research subject group en
Biomedical engineering
Research subject group fr
Génie biomédical
Research subject en
Biomedical engineering
Research subject fr
Génie biomédical
Partie
2
Nb partie
2
Application title
Intraoperative calibration (iCAL) fro prostate brachytherapy
Keyword
NSERC
Application summary
Prostate cancer is the second most common cancer in North American men. Brachytherapy, applied in about 55,000 cases annually in North America, entails the permanent implantation of radioactive sources into the prostate, under real-time ultrasound image guidance. Although brachytherapy has resulted in an improved prognosis, radiation toxicity remains a significant challenge. Brachytherapy systems require careful calibration to ensure the correct spatial relationship between the implant needles and the ultrasound image. Incorrect calibration leads to faulty delivery of the radiation dose, reducing the efficacy of cancer control and directly contributing to negative side effects like rectal ulcers and incontinence.
Calibration today is a costly, laborious and manual process, involving a great deal of subjective judgment by the operator. It is performed periodically, outside the operating room, with the assumption that calibration parameters remain valid over time. In reality, however, calibration parameters change during storage, transportation and setup of the equipment. Calibration errors are virtually impossible to detect during the procedure so the surgeon can never be certain whether the system is functioning correctly.
To improve contemporary practice, we calibrate the system in the operating room while the patient is being prepared for surgery. Our method is fast, fully automated and based on computations alone, eliminating subjectivity and human error. From our research in NSERC I2I Phase-I, we demonstrated the concept and prototype. Under the Phase-IIb grant, we will create a fully functional brachytherapy calibration system, field test it and bring it to readiness for commercial distribution. The resulting product will simultaneously reduce treatment costs, increase safety and improve the accuracy of prostate cancer brachytherapy.
The commercial partner for this proposal is Precision Therapeutics Inc. (PTI), a medical device company based in Kingston, Ontario. PTI develops ultrasound image guided systems for the diagnosis and treatment of prostate cancer. Through established strategic alliances, PTI has direct access to the prostate brachytherapy market in North America and worldwide.