Hydrogel Spacer Prospective Multicenter Randomized Controlled Pivotal Trial: Dosimetric and Clinical Effects of Perirectal Spacer Application in Men Undergoing Prostate Image Guided Intensity Modulated Radiation Therapy

Neil Mariados(SUNY Upstate Medical University), John Sylvester(21st Century Oncology (United States)), Dhiren Shah(Urology Associates), Lawrence I. Karsh(The Urology Center of Colorado), Richard Hudes(Chesapeake Urology Associates), David Beyer(Arizona Oncology), Steven Kurtzman(Urology Associates), Jeffrey A. Bogart(SUNY Upstate Medical University), R.A. Hsi(Peninsula Cancer Center), Michael Kos, Rodney J. Ellis(University Hospitals Cleveland Medical Center), Mark D. Logsdon(Sutter Health), S.H. Zimberg(Advanced Radiation Centers of New York), Kevin Forsythe(Oregon Urology Institute), Hong Zhang(University of Rochester), Edward Soffen(CentraState Healthcare Foundation), Patrick Francke(21st Century Oncology (United States)), C.A. Mantz(21st Century Oncology (United States)), Peter J. Rossi(Emory University), Theodore L. DeWeese(Johns Hopkins University), Daniel A. Hamstra(University of Michigan), Walter Bosch(Washington University in St. Louis), Hiram A. Gay(Washington University in St. Louis), Jeff M. Michalski(Washington University in St. Louis)
International Journal of Radiation Oncology*Biology*Physics
April 23, 2015
Cited by 422Open Access
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Abstract

PURPOSE: Perirectal spacing, whereby biomaterials are placed between the prostate and rectum, shows promise in reducing rectal dose during prostate cancer radiation therapy. A prospective multicenter randomized controlled pivotal trial was performed to assess outcomes following absorbable spacer (SpaceOAR system) implantation. METHODS AND MATERIALS: Overall, 222 patients with clinical stage T1 or T2 prostate cancer underwent computed tomography (CT) and magnetic resonance imaging (MRI) scans for treatment planning, followed with fiducial marker placement, and were randomized to receive spacer injection or no injection (control). Patients received postprocedure CT and MRI planning scans and underwent image guided intensity modulated radiation therapy (79.2 Gy in 1.8-Gy fractions). Spacer safety and impact on rectal irradiation, toxicity, and quality of life were assessed throughout 15 months. RESULTS: Spacer application was rated as "easy" or "very easy" 98.7% of the time, with a 99% hydrogel placement success rate. Perirectal spaces were 12.6 ± 3.9 mm and 1.6 ± 2.0 mm in the spacer and control groups, respectively. There were no device-related adverse events, rectal perforations, serious bleeding, or infections within either group. Pre-to postspacer plans had a significant reduction in mean rectal V70 (12.4% to 3.3%, P<.0001). Overall acute rectal adverse event rates were similar between groups, with fewer spacer patients experiencing rectal pain (P=.02). A significant reduction in late (3-15 months) rectal toxicity severity in the spacer group was observed (P=.04), with a 2.0% and 7.0% late rectal toxicity incidence in the spacer and control groups, respectively. There was no late rectal toxicity greater than grade 1 in the spacer group. At 15 months 11.6% and 21.4% of spacer and control patients, respectively, experienced 10-point declines in bowel quality of life. MRI scans at 12 months verified spacer absorption. CONCLUSIONS: Spacer application was well tolerated. Increased perirectal space reduced rectal irradiation, reduced rectal toxicity severity, and decreased rates of patients experiencing declines in bowel quality of life. The spacer appears to be an effective tool, potentially enabling advanced prostate RT protocols.


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