CyberKnife Prostate Clinical Trial

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Prostate HDR Brachytherapy versus Prostate CyberKnife: Practical Comparison
Donald B. Fuller, M.D., April 17, 2008

Prostate Abstract Summary

Comparison HDR Brachytherapy CyberKnife
 
   DOSE DELIVERY

   Radiobiological Power (Hypofractionation)

Yes Yes

   May deliver identical radiation fractionation

Yes Yes

   Dose molding matches cancer distribution

Yes Yes

   Spares urethra from high dose\

Yes Yes

   Able to curve dose around rectum

Yes Yes

   Can modulate dose to spare nerves

Yes Yes

   Typical Accuracy

+/- 1 mm* +/- 1 mm**
 
SPECIFIC PROCEDURAL ASPECTS

   Hospitalization

Yes No

   Invasive

Yes No

   Operating Room

Yes No

   Pain Management

Yes No

   Follow-up protocol after completion

Comparable Comparable

   Pubic bones block HDR catheter placement

Occasional Not a factor
 
   SIDE EFFECTS

   Organs affected

Primarily urological Primarily urological

   Typical magnitude

Mild to moderate Mild to moderate

   Erectile Preservation

Favorable Favorable

   Complications

Rare Rare
 
OUTCOME ASSESSMENT

   PSA Response Year One

Appears identical Appears identical

   PSA Response Intermediate-term (2-3 yr)

Appears identical Appears identical

   PSA Response Long-term (>= 5 years)

Durable Not defined yet


*   Potential source of error > 1 mm – HDR delivery catheter migration; prostate swelling
**   Potential source of error > 1 mm – Prostate rotation and deformation

Summary: The radiation dose molding and delivery accuracy properties of HDR brachytherapy and CyberKnife radiosurgery are extremely similar. CyberKnife is more patient friendly in the short run. HDR brachytherapy has long-term documentation of durable efficacy, which CyberKnife presently lacks, due to the newness of the technology. Because of the capability of CyberKnife to effectively “clone” HDR brachytherapy radiation dose distribution and fractionation, there is an expectation that it will produce an identical long-term efficacy result compared with HDR brachytherapy, when used in comparably selected patients, pending confirmation by clinical trials.

Written by Donald B. Fuller, M.D. – Radiation Oncologist

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