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Dose differentiated high-dose-rate prostate brachytherapy: a feasibility assessment of MRI-guided dose escalation to dominant intra-prostatic lesions.
Luminais, Christopher K; Nourzadeh, Hamidreza; Aliotta, Eric; Ward, Kristin; Cousins, David; Showalter, Timothy N; Libby, Bruce.
Afiliación
  • Luminais CK; Department of Radiation Oncology, University of Virginia, Charlottesville, Virginia, USA.
  • Nourzadeh H; Department of Radiation Oncology, University of Virginia, Charlottesville, Virginia, USA.
  • Aliotta E; Department of Radiation Oncology, University of Virginia, Charlottesville, Virginia, USA.
  • Ward K; Department of Radiation Oncology, University of Virginia, Charlottesville, Virginia, USA.
  • Cousins D; Department of Radiation Oncology, University of Virginia, Charlottesville, Virginia, USA.
  • Showalter TN; Department of Radiation Oncology, University of Virginia, Charlottesville, Virginia, USA.
  • Libby B; Moffitt Cancer Center, University of South Florida, USA.
J Contemp Brachytherapy ; 14(5): 423-428, 2022 Oct.
Article en En | MEDLINE | ID: mdl-36478705
ABSTRACT

Purpose:

Prostate brachytherapy is routinely performed with trans-rectal ultrasound (TRUS)- or computed tomography (CT)-based planning that cannot delineate dominant intra-prostatic lesions (DILs). In contrast, magnetic resonance imaging (MRI)-based planning allows for more accurate DIL delineation and dose escalation. This study assessed the maximum achievable dose escalation to DILs. Material and

methods:

We retrospectively identified 24 patients treated with high-dose-rate (HDR) prostate brachytherapy boost (15 Gy in 1 fraction). All patients had a pre-treatment prostate MRI with 1-3 DILs. MRIs were used to delineate DILs and were co-registered to TRUS intra-procedure. Treatment plans were experimentally re-optimized to escalate DIL dose. Dosimetric indices from the original and re-optimized plans were compared using two-tailed paired t-test. Re-optimized plans were deemed acceptable if they achieved all of the following criteria prostate D90 > 100%, prostate V100 > 90%, urethra D10 < 118%, rectum V80 < 0.5 cc, bladder D1cc < 75%, or if they did not exceed organs at risk (OARs) doses of the original plan.

Results:

The mean DIL D90 was significantly increased from 134% of the prescription dose on the original plans to 154% on the re-optimized plans. The mean urethra D10 and mean bladder D1cc were significantly reduced from 123% to 117% and from 72% to 65%, respectively. Prostate D90 was reduced from 106% to 102%, and prostate V100 was reduced from 93% to 91%.

Conclusions:

We re-optimized HDR brachytherapy plans to escalate DILs dose to a mean D90 of > 150% while maintaining favorable prostate coverage and OARs doses. We propose DIL D90 dose of > 150% (22.5 Gy) as an achievable goal.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Contemp Brachytherapy Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Contemp Brachytherapy Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
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