Radiotherapy provider Nucletron has received Food and Drug Administration 510(k) clearance for its Swift real-time intraoperative treatment-planning system for high-dose brachytherapy prostate cancer treatment. Swift, which is based on live ultrasound imaging, allows clinicians to generate a 3-D volume, create a treatment plan, place needles, evaluate and optimize needle placement and treatment dosages, and begin patient treatment within one hour, according to the Veenendaal, Netherlands-based firm.
Clinicians can use Swift to create a conformal treatment plan during the implantation procedure, allowing needle adjustment while in the operating room. This opens up the possibility of a first treatment being given while the patient is still in the operating room, Nucletron said.
By AuntMinnie.com staff writers
August 21, 2003
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