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작성일 : 14-12-26 10:16
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MEDIA ALERT - Mevion and Philips Radiation Oncology Systems collaborate to offer advanced treatment planning solutions for Mevion’s new pencil beam scanning technology
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 http://www.mevion.com/news/1079-new-pencial-bearm-technology [2130] |
Companies to Develop Pinnacle³ Proton Planning for the MEVION S250 Proton Therapy System Featuring HYPERSCAN
October 27, 2014 – Mevion Medical Systems and Philips Radiation Oncology Systems are collaborating to combine the treatment planning capability of Philips’ Pinnacle³ radiation therapy planning system with the MEVION S250 solution with HYPERSCAN, Mevion’s new pencil beam scanning technology that is capable of scanning a tumor in seconds.
Pinnacle³ currently supports the MEVION S250, the world’s smallest proton therapy platform. The new collaboration will focus on enabling the Pinnacle³ system to also support HYPERSCAN.
“HYPERSCAN is an advanced form of pencil-beam scanning and is only available on the MEVION S250. Since Pinnacle³ is already being used by certain Mevion S250 users, it’s only fitting that we work together to develop planning for HYPERSCAN,” said Joe Jachinowski, the president and chief executive officer of Mevion Medical Systems.
“We’re really pleased to be collaborating with Mevion as it introduces HYPERSCAN,” said Sue Wallace, PhD, general manager of Philips Radiation Oncology Systems. “At Philips, treatment planning is a critical element of informed therapy guidance, and the integration of Philips imaging and planning with therapy delivery systems is essential.”
The first site to use Pinnacle³ with the MEVION S250 is the UF Health Cancer Center at Orlando Health. Omar Zeidan, PhD, the center’s chief of proton therapy physics, noted, “The collaboration between Philips and Mevion will give world-class cancer centers like ours the ability to offer patients all the benefits of HYPERSCAN combined with the accuracy and reliability of Pinnacle³.” Zeidan added, “This will help lead to well-planned and well-executed proton therapy sessions that accurately target tumors.”
HYPERSCAN has not been cleared by the USFDA for clinical use.
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