Dosimetric feasibility of stereotactic irradiation of primary prostate cancer at 5x9 Gy with a method of urethral sparing.


Journal

The British journal of radiology
ISSN: 1748-880X
Titre abrégé: Br J Radiol
Pays: England
ID NLM: 0373125

Informations de publication

Date de publication:
01 Nov 2021
Historique:
pubmed: 21 7 2021
medline: 30 10 2021
entrez: 20 7 2021
Statut: ppublish

Résumé

The most commonly used dose for prostate cancer stereotactic body radiotherapy (SBRT) is 5 × 7.25 Gy. The aim of this study was to evaluate the dosimetric feasibility of a 5 × 9 Gy SBRT regimen while still limiting the dose to the urethra to 5 × 7.25 Gy. This dosimetric study is part of the groundwork for a future Phase III randomized trial. The prostate, the urethra and the tumors were delineated on 20 dosimetric CT-scans with MRI-registration. The planning target volume (PTVp) was defined as a 5 mm expansion (3 mm posteriorly) of the prostate. The planning at risk volume (PRVu) was defined as a 2 mm expansion of the urethra. The tumors were delineated on the MRI (GTVt) and a 3 mm-margin was added to create a tumoral planning target volume (PTVt). IMRT plans were optimized to deliver 5 × 9 Gy to the PTVp, limiting the dose to the PRVu to 5 × 7.25 Gy. Results are presented using average (range) values. PTVp doses were D98% = 36.2 Gy (35.6-36.8), D2% = 46.9 Gy (46.5-47.5) and mean dose = 44.1 Gy (43.8-44.5). The dose to the PRVu was within tolerance limits for all 20 patients: V34.4Gy = 99.8% (99.2-100) and D5% = 38.7 Gy (38.6-38.8). Dose coverage of PTV-PRVu was D95% = 40.6 Gy (40.5-40.9), D5% = 46.6 Gy (46.2-47.2) and mean dose = 44.6 Gy (44.3-44.9). Dose to the PTVt reached 44.6 Gy (41.2-45.9). Doses to the OAR were respected, except V36Gy ≤1 cc for the rectum. A SBRT dose-escalation to 5 × 9 Gy on the prostate while sparing the urethra + 2 mm at 36.25 Gy is feasible without compromising dose coverage to the tumor. This radiation regimen will be used for a Phase-III trial. In prostate SBRT, dose optimization on the urethra is feasible and could decrease urinary toxicities.

Identifiants

pubmed: 34283647
doi: 10.1259/bjr.20210142
pmc: PMC8553191
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

20210142

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Auteurs

Salim Benhmida (S)

Department of Radiation Oncology, Centre Hospitalier Lyon Sud, Pierre Benite, France.

Amandine Beneux (A)

Department of Medical Physics and Radioprotection, Centre Hospitalier Lyon Sud, Pierre Benite, France.

Corina Udrescu (C)

Department of Radiation Oncology, Centre Hospitalier Lyon Sud, Pierre Benite, France.

Olivier Rouviere (O)

Department of Urological Radiology, Hopital Edouard Herriot, Lyon, France.

Samy Horn (S)

Department of Radiation Oncology, Centre Hospitalier Lyon Sud, Pierre Benite, France.

Ciprian Enachescu (C)

Department of Radiation Oncology, Centre Hospitalier Lyon Sud, Pierre Benite, France.

Ariane Lapierre (A)

Department of Radiation Oncology, Centre Hospitalier Lyon Sud, Pierre Benite, France.

Olivier Chapet (O)

Department of Radiation Oncology, Centre Hospitalier Lyon Sud, Pierre Benite, France.

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