Dosimetric impact of organ at risk daily variation during prostate stereotactic ablative radiotherapy.


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:
Apr 2020
Historique:
pubmed: 24 1 2020
medline: 27 3 2020
entrez: 24 1 2020
Statut: ppublish

Résumé

Prostate stereotactic ablative radiotherapy (SABR) delivers large doses using a fast dose rate. This amplifies the effect geometric uncertainties have on normal tissue dose. The aim of this study was to determine whether the treatment dose-volume histogram (DVH) agrees with the planned dose to organs at risk (OAR). 41 low-intermediate risk prostate cancer patients were treated with SABR using a linac based technique. Dose prescribed was 35 Gy in five fractions delivered on alternate days, planned using volumetric modulated arc therapy (VMAT) with 10X flattening filter free (FFF). On treatment, prostate was matched to fiducial markers on cone beam CT (CBCT). OAR were retrospectively delineated on 205 pre-treatment CBCT images. Daily CBCT contours were overlaid on the planning CT for dosimetric analysis. Verification plan used to evaluate the daily DVH for each structure. The daily doses received by OAR were recorded using the D%. The median rectum and bladder volumes at planning were 67.1 cm In this cohort of prostate SABR patients, we estimate the OAR treatment DVH was higher than planned. This was due to rectal and bladder organ variation. OAR variation in prostate SABR using a FFF technique, may cause the treatment DVH to be higher than planned.

Identifiants

pubmed: 31971829
doi: 10.1259/bjr.20190789
pmc: PMC7362910
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

20190789

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Auteurs

Lynsey Devlin (L)

Department of Clinical Oncology, Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.

David Dodds (D)

Department of Clinical Oncology, Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.

Azmat Sadozye (A)

Department of Clinical Oncology, Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.

Philip McLoone (P)

Institute of Health & Wellbeing, University of Glasgow, Glasgow, United Kingdom.

Nicholas MacLeod (N)

Department of Clinical Oncology, Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.

Carolynn Lamb (C)

Department of Clinical Oncology, Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.

Suzanne Currie (S)

Department of Clinical Physics and Bioengineering, Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.

Stefanie Thomson (S)

Department of Clinical Physics and Bioengineering, Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.

Aileen Duffton (A)

Department of Clinical Oncology, Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.

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