A multi-institutional clinical trial of rectal dose reduction via injected polyethylene-glycol hydrogel during IMRT for prostate cancer: Analysis of dosimetric outcomes.
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Song, Danny Y.
Johns Hopkins School of Medicine, Baltimore, MD
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Herfarth, Klaus
Department of Radiooncology, University of Heidelberg, Heidelberg, Germany
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Uhl, Matthias
Department of Radiooncology, University of Heidelberg, Heidelberg, Germany
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Eble, Michael J.
Rheinisch-Westfaelische Technische Hochschule Aachen, Aachen, Germany
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Pinkawa, Michael
Rheinisch-Westfaelische Technische Hochschule Aachen, Aachen, Germany
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Van Triest, Baukelien
Netherlands Cancer Institute, Amsterdam, Netherlands
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Kalisvaart, Robin
Netherlands Cancer Institute/Antoni van Leeuwenhoek ziekenhuis, Amsterdam, Netherlands
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Weber, Damien C.
Geneva University Hospital, Department of Radiation Oncology and Centre de Recherche Clinique Dubois Ferrière Dinu Lipati, Geneva, Switzerland
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Miralbell, Raymond
Geneva University, Geneva, Switzerland
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DeWeese, Theodore L.
Johns Hopkins University School of Medicine, Baltimore, MD
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Ford, Eric
University of Washington Medical Center, Seattle, WA
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Published in:
- Journal of Clinical Oncology. - American Society of Clinical Oncology (ASCO). - 2013, vol. 31, no. 6_suppl, p. 35-35
English
35 Background: To characterize the effect of a prostate-rectum spacer on dose to rectum during external beam radiotherapy for prostate cancer, and to assess for factors correlated with rectal dose reduction. Methods: Fifty-two patients at 4 institutions were enrolled onto a prospective pilot clinical trial. Patients underwent baseline scans, then were injected with perirectal spacing hydrogel and re-scanned. IMRT plans were created on both scans for comparison. Objectives were to establish rates of creation of ≥7.5mm of prostate-rectal separation, and decrease in rectal V70 of ≥25%. Multiple regression analysis was performed to evaluate associations between pre- vs. post-injection changes in rectal V70 and changes in plan conformity, rectal volume, bladder volume, bladder V70, PTV volume, as well as post-injection mid-gland separation, gel volume, gel thickness, length of PTV/gel contact, or gel left-to-right symmetry. Results: Hydrogel resulted in > 7.5mm prostate-rectal separation in 95.8% of patients; 95.7% had decreased rectal V70 of > 25%, with mean reduction of 8.0 Gy. There were no significant differences in pre- and post-injection prostate, PTV, rectal, and bladder volumes. Plan conformities were significantly different pre- vs. post-injection (P = 0.02). In multiple regression analysis, change in plan conformity was negatively associated with reduction in V70 (P=0.01); plans with worse conformity indexes post-injection compared to pre-injection (n=13) still had improvements in rectal V70. Reductions in V70 did not significantly vary by institution, despite significant inter-institutional variations in plan conformity. There were no significant relationships between reduction in V70 and the other characteristics analyzed. Conclusions: Injection of hydrogel into prostate-rectal interface resulted in dose reductions to rectum for > 90% of patients treated. Rectal sparing was statistically significant across a range of 10-75 Gy, and was demonstrated within the presence of significant inter-institutional variability in plan conformity, target definitions, and injection results.
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green
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https://folia.unifr.ch/global/documents/161289
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