Twelve-month prostate volume reduction after MRI-guided transurethral ultrasound ablation of the prostate.


Journal

European radiology
ISSN: 1432-1084
Titre abrégé: Eur Radiol
Pays: Germany
ID NLM: 9114774

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 08 01 2018
accepted: 01 06 2018
revised: 08 05 2018
pubmed: 27 6 2018
medline: 12 2 2019
entrez: 27 6 2018
Statut: ppublish

Résumé

To quantitatively assess 12-month prostate volume (PV) reduction based on T2-weighted MRI and immediate post-treatment contrast-enhanced MRI non-perfused volume (NPV), and to compare measurements with predictions of acute and delayed ablation volumes based on MR-thermometry (MR-t), in a central radiology review of the Phase I clinical trial of MRI-guided transurethral ultrasound ablation (TULSA) in patients with localized prostate cancer. Treatment day MRI and 12-month follow-up MRI and biopsy were available for central radiology review in 29 of 30 patients from the published institutional review board-approved, prospective, multi-centre, single-arm Phase I clinical trial of TULSA. Viable PV at 12 months was measured as the remaining PV on T2-weighted MRI, less 12-month NPV, scaled by the fraction of fibrosis in 12-month biopsy cores. Reduction of viable PV was compared to predictions based on the fraction of the prostate covered by the MR-t derived acute thermal ablation volume (ATAV, 55°C isotherm), delayed thermal ablation volume (DTAV, 240 cumulative equivalent minutes at 43°C thermal dose isocontour) and treatment-day NPV. We also report linear and volumetric comparisons between metrics. After TULSA, the median 12-month reduction in viable PV was 88%. DTAV predicted a reduction of 90%. Treatment day NPV predicted only 53% volume reduction, and underestimated ATAV and DTAV by 36% and 51%. Quantitative volumetry of the TULSA phase I MR and biopsy data identifies DTAV (240 CEM43 thermal dose boundary) as a useful predictor of viable prostate tissue reduction at 12 months. Immediate post-treatment NPV underestimates tissue ablation. • MRI-guided transurethral ultrasound ablation (TULSA) achieved an 88% reduction of viable prostate tissue volume at 12 months, in excellent agreement with expectation from thermal dose calculations. • Non-perfused volume on immediate post-treatment contrast-enhanced MRI represents only 64% of the acute thermal ablation volume (ATAV), and reports only 60% (53% instead of 88% achieved) of the reduction in viable prostate tissue volume at 12 months. • MR-thermometry-based predictions of 12-month prostate volume reduction based on 240 cumulative equivalent minute thermal dose volume are in excellent agreement with reduction in viable prostate tissue volume measured on pre- and 12-month post-treatment T2w-MRI.

Identifiants

pubmed: 29943185
doi: 10.1007/s00330-018-5584-y
pii: 10.1007/s00330-018-5584-y
doi:

Types de publication

Clinical Trial, Phase I Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

299-308

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Auteurs

David Bonekamp (D)

Department of Radiology (E010), German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany. d.bonekamp@dkfz-heidelberg.de.

M B Wolf (MB)

Department of Radiology (E010), German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.

M C Roethke (MC)

Department of Radiology (E010), German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.

S Pahernik (S)

Department of Urology, University Hospital Heidelberg, Heidelberg, Germany.

B A Hadaschik (BA)

Department of Urology, University Hospital Heidelberg, Heidelberg, Germany.

G Hatiboglu (G)

Department of Urology, University Hospital Heidelberg, Heidelberg, Germany.

T H Kuru (TH)

Department of Urology, University Hospital Heidelberg, Heidelberg, Germany.

I V Popeneciu (IV)

Department of Urology, University Hospital Heidelberg, Heidelberg, Germany.

J L Chin (JL)

Department of Urology, University of Western Ontario (UWO), London Health Sciences Center, Victoria Hospital, London, ON, Canada.

M Billia (M)

Department of Urology, University of Western Ontario (UWO), London Health Sciences Center, Victoria Hospital, London, ON, Canada.

J Relle (J)

Department of Urology, Beaumont Health System, Royal Oak, MI, USA.

J Hafron (J)

Department of Urology, Beaumont Health System, Royal Oak, MI, USA.

K R Nandalur (KR)

Department of Radiology, Beaumont Health System, Royal Oak, MI, USA.

R M Staruch (RM)

Clinical Science, Profound Medical Inc., Toronto, ON, Canada.

M Burtnyk (M)

Clinical Science, Profound Medical Inc., Toronto, ON, Canada.

M Hohenfellner (M)

Department of Urology, University Hospital Heidelberg, Heidelberg, Germany.

H-P Schlemmer (HP)

Department of Radiology (E010), German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.

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Classifications MeSH