CT lung cancer screening approved by CMS

The U.S. Centers for Medicare and Medicaid Services (CMS) approved CT lung cancer screening, stating evidence is sufficient to justify screening for high-risk individuals.

Press release: CT lung cancer screening approved by CMS

Bremen/Germany, November 11, 2014 - Yesterday the U.S. Centers for Medicare and Medicaid Services (CMS) approved CT lung cancer screening, stating evidence is sufficient to justify screening for high-risk individuals. This decision - long awaited after the USPSTF grade B recommendation last year and the MEDCAC panel hearing in April - will finally clear the path to implement CT based lung cancer screening in the U.S. for the general public.

Lung cancer is the leading cancer killer. It causes more deaths than colon, breast, and pancreatic cancer combined. The prime challenge is that patients often present only when their condition is symptomatic - at a stage, where treatment has become difficult. Results of the U.S. National Lung Screening Trial (NLST) show a 20 percent reduction in mortality due to early detection provided by CT screening. Even though European studies like the Dutch-Belgian "Nelson" are still being evaluated, it is expected that European countries will follow in the near future.

With the CMS decision, lung screening will become available to over 8 million Americans. Providers of imaging services will have to overcome the challenge of handling the related workload. Precise reading tools, standardized reporting and efficient workflows will be needed to ensure diagnostic precision and cost effectiveness.

With Veolity, the medical software specialist MeVis Medical Solutions AG in Bremen/Germany, provides a dedicated workstation for lung cancer screening. Based on leading-edge research, Veolity optimizes reading workflows. It brings together lung CAD - computer-aided detection - of solid pulmonary nodules approved by the FDA, integration and automatic registration of prior studies, and efficient, state-of-the-art reporting. Reports are generated automatically according to current standards and guidelines, including current models for nodule malignancy prediction. Automated measurements, integration of incidental findings, determination of patient follow-up, and integration of screening worklists make the system a complete solution for reading lung screening CT data.

"Making CT lung screening available to high-risk population will be saving thousands of lives every year. We highly welcome this decision, not only because it sparks additional interest in our products, but mainly because of the tremendous benefit for the patients.", explains Bernd Kuemmerlen, Product Manager, MeVis Medical Solutions AG. "With Veolity, we aim to make the workload for the radiologists manageable, while at the same time improving quality and thus the benefit for the patient. Finding, measuring and comparing nodules to prior exams manually is tedious work. Veolity automates most of these steps, ensuring diagnostic precision by detecting nodules, providing objective measurements, and comparing with prior findings."

About
Veolity Veolity is the first dedicated workstation for lung cancer screening. Its features include FDA-approved vendor-neutral computer-aided detection (CAD) of lung nodules, automated measuring of nodules, integration and registration of prior studies, and reporting based on standards and guidelines.
www.veolity.com

Meet MeVis Medical Solutions AG at RSNA 2014
MeVis will showcase Veolity and further solutions for radiologists at booth 2965-F, in hall A, South Building, German Pavilion.
www.rsna.org

About MeVis Medical Solutions AG
www.mevis.de

Contact:
MeVis Medical Solutions AG
Press Relations
Martina Hallmann
Caroline-Herschel-Str. 1
28359 Bremen, Germany
Phone: +49 421 22495-301
E-mail: martina.hallmann(at)mevis.de

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