BTG, Mirada’s cancer treatment planning software nabs CE mark

London

Interventional medicine player BTG and imaging company Mirada Medical earned a CE mark for their dosimetry software for the planning of selective internal radiation therapy (SIRT) for patients with liver cancer.

The Simplicit90Y software offers digital processing, review and reporting of medical imaging, along with image manipulation and quantification analysis capabilities, according to a statement. These features allow for more standardized and consistent dosimetry planning for Yttrium-90 (90Y) SIRT and for the personalization of each patient’s treatment. The software is intended for nuclear medicine or radiology practitioners to process data from images from planar scans and tomographic scans, according to the statement.

“Dosimetry can be a time intensive and complex process and Simplicity90Y simplifies both dosimetry and post-treatment validation,” said Dr. Etienne Garin, chair professor of Nuclear Medicine, Cancer Institute, Centre Eugene Marquis Rennes, in the statement. “Knowing you can use this intuitive software to help deliver a more personalised treatment for each patient, achieving the best dose of 90Y radiation to the tumour while minimising exposure to healthy tissue, gives physicians more confidence.”

Event

Join the world's top medtech executives virtually for the leading event in medtech — The Virtual MedTech Conference by AdvaMed

Expect the same high-quality education, world-class speakers and valuable business development in a virtual format. Experience more of the conference with on demand content and partnering, as well as livestreamed sessions.

BTG markets a number of interventional oncology products, including TheraSphere, glass microspheres that deliver a targeted dose of Yttrium-90 to a tumor while minimizing harm to healthy tissue. It also markets the LC Bead Lumi, a radiopaque embolic bead for the embolization of hypervascular tumors, or the disruption of blood flow to such tumors to enable their shrinkage.

BTG teamed up with Philips in February this year to roll out the LC Bead Lumi in the U.S. The device is an upgrade to the LC Bead, which is not visible via imaging.

Read more on

Suggested Articles

Takeda tapped Roche’s Foundation Medicine to develop tissue- and blood-based companion diagnostic tests for its portfolio of lung cancer therapies.

Cellex has announced plans to develop a rapid coronavirus test that people can fully perform at home, from sample collection to result, using an app.

More than 20 states either don’t release or have incomplete data on the rapid antigen tests now considered key to containing the coronavirus.