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                              Installation of Elekta MR-linac initiated at Sunnybrook Health Sciences Centre

                              July 13, 2017
                              Transformative magnetic resonance radiation therapy system will focus on advanced image-guided radiotherapy for cancer patients 

                              TORONTO, July 13, 2017 – Elekta (EKTA-B.ST) and Sunnybrook Health Sciences Centre have initiated installation of Elekta’s MR-linac, an investigational magnetic resonance radiation therapy (MR/RT) system at the Odette Cancer Centre, Sunnybrook Health Sciences Centre in Toronto.

                              “This new equipment will allow us to better understand tumor response during treatment and give us a way of looking at the tumor that was not possible before,” said Dr. Gregory Czarnota, head of radiation oncology at Odette Cancer Centre.

                              The MR-linac is the only MR/RT system that integrates a premium (1.5 Tesla) MR scanner with an advanced linear accelerator and intelligent software. It is expected to deliver precisely targeted radiation doses while simultaneously capturing high-quality MR images, which will allow clinicians to visualize tumors at any time and adapt the treatment accordingly. 

                              “Real-time understanding of tumor response will help us adjust treatment, focus radiation on tumors with pinpoint precision, and spare healthy tissue from radiation,” said Dr. Arjun Sahgal, head of Odette’s Cancer Ablation Therapy Program. “We are proud of all the work that has taken place to bring this technology to Sunnybrook.”

                              Sunnybrook is a member of Elekta’s MR-linac Consortium, a global collaboration of institutions focused on uniting leaders in radiation oncology, MR-imaging, physics and radiotherapists. The mission of the Consortium is to investigate how MR-linac technology can lead to improved patient outcomes for existing radiation therapy indications and extend radiation therapy for additional indications.

                              Elekta introduced the MR-linac technology under the name of Unity during the ESTRO congress in Vienna, Austria in April this year.

                              Installation of Elekta’s MR-linac is complete at the six other consortium member sites including: University Medical Center Utrecht, the Netherlands; 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; the Froedtert & Medical College of Wisconsin Clinical Cancer Center at Froedtert Hospital, Milwaukee, Wisconsin; and The Christie NHS Foundation Trust, Manchester, UK.

                              Sunnybrook is the lead consortium site for developing applications of the MR-linac in the treatment of glioblastoma, the most common malignant brain tumor in adults. Dr. Sahgal and his team have developed a protocol to evaluate advanced imaging for primary cancers of the brain and have designed a clinical trial that will explore using the technology to adapt the radiation dose delivered to primary brain tumors on a daily basis. Sunnybrook anticipates that it will initiate patient treatments once the device is Health Canada approved.

                              “Sunnybrook is a leading innovator of advanced radiation therapies, and its support and commitment have been instrumental to our ongoing efforts to realize the potential of magnetic resonance radiation therapy,” said Kevin Brown, Elekta’s Global Vice President of Scientific Research. “Initiating installation of the MR-linac system at Odette Cancer Centre, the final consortium site to come on line, is an important milestone in the development of this transformative technology. We look forward to the contributions that Sunnybrook will make to advance the care of patients with glioblastoma.”

                              Elekta Unity is the only MR/RT system that integrates a premium quality (1.5 Tesla) MR scanner, from MR technology partner Philips, with an advanced linear accelerator and intelligently designed software. To learn more, visit www.elekta.com/Unity.

                              Elekta Unity 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, e-mail: gert.vansanten@elekta.com
                              Time zone: CET: Central European Time

                              Raven Canzeri, Global Public Relations Manager
                              Tel: +1 770 670 2524, e-mail: raven.canzeri@elekta.com
                              Time zone: ET: Eastern 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.