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                                  Members of the Elekta MR-linac Consortium present updates on magnetic resonance radiation therapy (MR/RT) at the ASTRO Annual Meeting

                                  September 27, 2017
                                  Consortium studies include evaluation of MR/RT in brain cancer and its potential to reduce treatment volumes and protect healthy tissue in response to tumor shape changes during radiation therapy

                                  Elekta (EKTA-B.ST) today announced that members of the Elekta MR-linac Consortium reported data related to the advancement of the company’s transformative MR/RT system at the American Society for Radiation Oncology (ASTRO) Annual Meeting, September 24-27 in San Diego.

                                  The Elekta MR-linac is the only MR/RT system that integrates a high-field (1.5 Tesla) MR scanner with an advanced linear accelerator and intelligently-designed software. The system is expected to deliver precisely targeted radiation doses while simultaneously capturing the highest-quality MR images. These features are expected to allow clinicians to visualize tumors at any time and adapt treatment.

                                  “The Consortium continues to make excellent progress in establishing MR/RT as a new approach to radiation therapy,” said Kevin Brown, Global VP Scientific Research at Elekta. “In bringing together clinicians, researchers and medical physicists and leading international cancer centers, the Consortium has developed truly innovative approaches to integrating the most advanced MR imaging and linear accelerator technologies. We deeply value their ongoing efforts to enable MR/RT as the next step in the evolution of radiation therapy.”

                                  Researchers at the Odette Cancer Centre, Sunnybrook Health Sciences Centre in Toronto, presented preliminary results of a study evaluating the potential of MR-linac in adapting to changes in tumor volume that can be observed using MR imaging during treatment of glioblastoma multiforme, an aggressive form of brain cancer (Abstract #3706). The study is designed to capture MR images from 20 patients at the treatment planning stage, at 10 and 20 days of radiation therapy and at one month following completion of treatment. Imaging data showing relative and absolute changes in gross tumor volume (GTV) are then used to simulate a new planning target volume (PTV) to assess the feasibility of treatment plan adaptation.

                                  Data for the first three patients evaluated in this study were presented by Sunnybrook’s Mark Ruschin, PhD, MCCPM. Two of the three patients showed decreases in GTV of 14% and 20% at Day 20 and 51% and 42% one month following completion of treatment. The image set containing the 20% GTV shrinkage at Day 20 was used to generate an adapted plan, resulting in a new PTV that was 31% smaller than the original. In the adapted plan, the smaller PTV contributed to a reduction in the maximum dose to the brainstem and optic chiasm by 37% and 39%, respectively. In addition to demonstrating a dosimetric advantage of adaptive brain radiotherapy, the present work is an important first step towards developing the tools and processes needed for clinical implementation of the new MR/RT technology. Future work involves the use of functional imaging to improve the quantification of tumor and normal tissue response to radiation and ultimately leads toward adapting treatment based on an individual patient’s biological response.

                                  “Reducing treatment volumes and sparing healthy tissue is a critical factor in improving the care and outcomes for patients treated with radiation therapy,” said Arjun Sahgal, MD, Deputy Chief of the Department of Radiation Oncology at Sunnybrook. “These preliminary data suggest that the integrated, high-field MR imaging capabilities of MR-linac could enable online plan adaptation in response to changes in tumor volume and surrounding structures during treatment. These adaptations could enable reduced treatment volumes and protection of critical organs and structures.”

                                  The potential of MR/RT to provide greater insights into the biology of cancer was also featured at the conference. Allen Li, PhD, Professor and Chief of Medical Physics at Froedtert & Medical College of Wisconsin moderated and participated in a panel discussion titled “MRI-guided adaptation: From anatomy to biology” (Panel 04). The discussion focused on recent advances in using MRI to assess treatment response and guide adaptive radiation therapy practices, including: a review of data that provide insight into using advanced MRI technologies to assess or monitor radiation therapy responses in selected tumor sites; algorithms and tools required for treatment plan adaptation based on treatment responses; and opportunities and challenges related to the use of advanced MRI in clinical practice.

                                  Additional abstracts related to the development of MR-linac presented at the conference include:

                                  • Quantifying complex abdominal organ motions in different time frames in radiation therapy (Abstract #3669)

                                  This abstract reports results of a study that investigated abdominal motion induced by respiration and peristalsis during various time durations relevant to radiation therapy. The study used a variety of CT and MRI techniques to acquire images of tumors and surrounding tissue in 31 patients with pancreatic or liver cancer. Images were captured while patients engaged in free breathing (FB) and breath hold (BH). Investigators conclude that the abdominal motions due to peristalsis in the time frames from seconds to minutes can be similar in magnitude to motion resulting from breathing. These motions can be irregular and persistent throughout the imaging and radiation therapy delivery procedures, and should be considered together with respiration motion during radiation therapy for abdominal tumors.

                                  • Acceleration of online adaptive replanning with workflow automation (Presentation #238)

                                  This abstract reports on the development of software tools to automate online adaptive re-planning (OARP) and the testing of these tools on both a conventional linear accelerator with an in-room CT scanner and an MR-linac. The research treatment-planning package has the ability to account for magnetic fields and includes fast replanning algorithms. The OARP process was broken down into five distinct modules: auto-segmentation based on daily CT or MRI scans; contour review and editing; adaptive plan generation; evaluation of the adaptive plan based on daily images; and transferring the new plan and performing quality assurance assessment prior to delivery. The automated tools and workflow were tested on 23 daily CT and MRI scans from five prostate cancer cases. Results show that OARP with the automation software tools, excluding the contour editing module, was 250 ±14 seconds, a 49% reduction in operation time compared with OARP conducted without the automated tools. The contour editing module, which was the most time consuming, ranged from five to ten minutes. Investigators conclude that the use of these automation tools substantially reduces the time for the online replanning process and eliminates user stresses and input errors during the online replanning process. The research team is working to improve the efficiency of the contour editing module.

                                  The founding members of the Elekta MR-linac Consortium are: University Medical Center Utrecht, the Netherlands (UMCU); The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, the Netherlands; The University of Texas MD Anderson Cancer Center, Houston, Texas; the Institute of Cancer Research, working with its clinical partner The Royal Marsden NHS Foundation Trust, London, England; Froedtert & the Medical College of Wisconsin Clinical Cancer Center at Froedtert Hospital, Milwaukee, Wisconsin; The Christie NHS Foundation Trust, Manchester, UK and the Odette Cancer Centre, Sunnybrook Health Sciences Centre in Toronto.

                                  To learn more about Elekta’s MR-linac, visit www.elekta.com.

                                  Elekta’s MR-linac is a work in progress and not available for sale or distribution.

                                  # # #

                                  For further information, please contact:
                                  Gert van Santen, Group Vice President Corporate Communications, Elekta AB
                                  Tel: +31 653 561 242, Email: [email protected]
                                  Time zone: CET: Central European Time
                                   
                                  Raven Canzeri, Global Public Relations Manager
                                  Tel: +1 770 670 2524, Email: [email protected]
                                  Time zone: EST: Eastern Standard Time
                                   
                                  About Elekta
                                  Elekta is proud to be the leading innovator of equipment and software used to improve, prolong and save the lives of people with cancer and brain disorders. Our advanced, effective solutions are created in collaboration with customers, and more than 6,000 hospitals worldwide rely on Elekta technology. Our treatment solutions and oncology informatics portfolios are designed to enhance the delivery of radiation therapy, radiosurgery and brachytherapy, and to drive cost efficiency in clinical workflows. Elekta employs 3,600 people around the world. Headquartered in Stockholm, Sweden, Elekta is listed on NASDAQ Stockholm. www.elekta.com

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                                  Important Safety Information: Radiation therapy is not appropriate for all patients. Radiation treatments may cause side effects that can vary depending on the part of the body being treated. In some patients, they can be severe. Treatment sessions may vary in complexity and time. Refer to individual product labeling (instructions for use) for more complete information on product safety and effectiveness for its intended use.