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Feasibility of dominant intraprostatic lesion boosting using advanced photon-, proton- or brachytherapy.

Authors :
Andrzejewski, Piotr
Kuess, Peter
Knäusl, Barbara
Pinker, Katja
Georg, Petra
Knoth, Johannes
Berger, Daniel
Kirisits, Christian
Goldner, Gregor
Helbich, Thomas
Pötter, Richard
Georg, Dietmar
Source :
Radiotherapy & Oncology. Dec2015, Vol. 117 Issue 3, p509-514. 6p.
Publication Year :
2015

Abstract

Background and purpose Advancements in imaging and dose delivery enable boosting of the dominant intraprostatic lesions (DIL), while maintaining organs-at-risk (OAR) tolerances. This study aimed to assess the feasibility of DIL boosting for volumetric modulated arc therapy (VMAT), intensity modulated proton therapy (IMPT) and high dose rate brachytherapy (HDR-BT). Material and methods DILs were defined on multiparametric magnetic resonance imaging and fused with planning CT for twelve patients. VMAT, IMPT and HDR-BT plans were created for each patient with an EQD2 α / β DIL aimed at 111.6 Gy, PTV initial D pres was 80.9 Gy (EBRT) with CTV D 90% = 81.9 Gy (HDR-BT). Hard dose constraints were applied for OARs. Results Higher boost doses were achieved with IMPT compared to VMAT, keeping major OAR doses at similar levels. Patient averaged EQD2 α / β D 50% to DIL were 110.7, 114.2 and 150.1 Gy(IsoE) for VMAT, IMPT and HDR-BT, respectively. Respective rectal wall D mean were 30.5 ± 5.0, 16.7 ± 3.6, 9.5 ± 2.5 Gy(IsoE) and bladder wall D mean were 21.0 ± 5.5, 15.6 ± 4.3 and 6.3 ± 2.2 Gy(IsoE). Conclusions DIL boosting was found to be feasible with all investigated techniques. Although OAR doses were higher than for standard treatment approach, the risk levels were reasonably low. HDR-BT was superior to VMAT and IMPT, both in terms of OAR sparing and DIL boosting. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01678140
Volume :
117
Issue :
3
Database :
Academic Search Index
Journal :
Radiotherapy & Oncology
Publication Type :
Academic Journal
Accession number :
111666244
Full Text :
https://doi.org/10.1016/j.radonc.2015.07.028