ALISO VIEJO, Calif. - Initial findings from the SAVI® Collaborative Research Project (SCRP), on SAVI radiation therapy for breast cancer, were presented at the recent annual meeting of the American Brachytherapy Society (ABS).

The SAVI Collaborative Research Project was established to produce additional research, presentations, and peer-reviewed, published literature on SAVI. The data collected thus far represents the largest subset of patients who have received accelerated partial breast irradiation (APBI) with the SAVI applicator.

The registry is lead by Catheryn Yashar, M.D., of the UC San Diego School of Medicine, and Robert R. Kuske, M.D., a pioneer in APBI and medical director at Arizona Breast Cancer Specialists.
"The SAVI registry is adding important scientific knowledge to the field of APBI," said Dr. Yashar, who presented the initial data in a podium presentation at ABS. "Because there are several forms of APBI, this research allows us to compare the various forms and better determine which devices are suited to particular types of patients."

The findings presented at ABS are the first to be reported from the SCRP. Based on a retrospective review of 294 patients treated at five clinical sites, researchers concluded the overall dosimetry of SAVI was excellent and that the data demonstrate SAVI's unique ability to sculpt the radiation dose away from the skin and ribs while selectively treating targeted tissue.

The SAVI multi-catheter applicator is available in four sizes designed to fit different surgical cavity sizes. The research presented at ABS showed that the two sizes used to treat larger cavities provide dosimetric coverage that is comparable to published data for various forms of "balloon" breast brachytherapy devices. The two sizes for women with smaller breasts and cavities were found to be useful in cases where anatomical restrictions might preclude use of a balloon device.

SAVI delivers accelerated partial breast irradiation APBI as part of breast conservation therapy (BCT). By specifically targeting radiation where the cancer is most likely to recur, SAVI reduces treatment time from six weeks with traditional whole-breast irradiation, to just five days.

The SAVI device allows physicians to customize radiation dose based on patient-specific anatomy, and is the ideal single-entry breast brachytherapy treatment method when the skin and ribs are close to the lumpectomy cavity. This unique ability can make the benefits of APBI available to twice as many women, as well as result in better outcomes including less skin toxicity, reduced risk of infection and improved cosmesis.

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