In-vivo treatment accuracy analysis of active motion-compensated liver SBRT through registration of plan dose to post-therapeutic MRI-morphologic alterations.


Journal

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
ISSN: 1879-0887
Titre abrégé: Radiother Oncol
Pays: Ireland
ID NLM: 8407192

Informations de publication

Date de publication:
05 2019
Historique:
received: 17 10 2018
revised: 18 01 2019
accepted: 19 01 2019
entrez: 22 4 2019
pubmed: 22 4 2019
medline: 28 3 2020
Statut: ppublish

Résumé

In-vivo-accuracy analysis (IVA) of dose-delivery with active motion-management (gating/tracking) was performed based on registration of post-radiotherapeutic MRI-morphologic-alterations (MMA) to the corresponding dose-distributions of gantry-based/robotic SBRT-plans. Forty targets in two patient cohorts were evaluated: (1) gantry-based SBRT (deep-inspiratory breath-hold-gating; GS) and (2) robotic SBRT (online fiducial-tracking; RS). The planning-CT was deformably registered to the first post-treatment contrast-enhanced T1-weighted MRI. An isodose-structure cropped to the liver (ISL) and corresponding to the contoured MMA was created. Structure and statistical analysis regarding volumes, surface-distance, conformity metrics and center-of-mass-differences (CoMD) was performed. Liver volume-reduction was -43.1 ± 148.2 cc post-RS and -55.8 ± 174.3 cc post-GS. The mean surface-distance between MMA and ISL was 2.3 ± 0.8 mm (RS) and 2.8 ± 1.1 mm (GS). ISL and MMA volumes diverged by 5.1 ± 23.3 cc (RS) and 16.5 ± 34.1 cc (GS); the median conformity index of both structures was 0.83 (RS) and 0.80 (GS). The average relative directional errors were ≤0.7 mm (RS) and ≤0.3 mm (GS); the median absolute 3D-CoMD was 3.8 mm (RS) and 4.2 mm (GS) without statistically significant differences between the two techniques. Factors influencing the IVA included GTV and PTV (p = 0.041 and p = 0.020). Four local relapses occurred without correlation to IVA. For the first time a method for IVA was presented, which can serve as a benchmarking-tool for other treatment techniques. Both techniques have shown median deviations <5 mm of planned dose and MMA. However, IVA also revealed treatments with errors ≥5 mm, suggesting a necessity for patient-specific safety-margins. Nevertheless, the treatment accuracy of well-performed active motion-compensated liver SBRT seems not to be a driving factor for local treatment failure.

Sections du résumé

BACKGROUND/PURPOSE
In-vivo-accuracy analysis (IVA) of dose-delivery with active motion-management (gating/tracking) was performed based on registration of post-radiotherapeutic MRI-morphologic-alterations (MMA) to the corresponding dose-distributions of gantry-based/robotic SBRT-plans.
METHODS
Forty targets in two patient cohorts were evaluated: (1) gantry-based SBRT (deep-inspiratory breath-hold-gating; GS) and (2) robotic SBRT (online fiducial-tracking; RS). The planning-CT was deformably registered to the first post-treatment contrast-enhanced T1-weighted MRI. An isodose-structure cropped to the liver (ISL) and corresponding to the contoured MMA was created. Structure and statistical analysis regarding volumes, surface-distance, conformity metrics and center-of-mass-differences (CoMD) was performed.
RESULTS
Liver volume-reduction was -43.1 ± 148.2 cc post-RS and -55.8 ± 174.3 cc post-GS. The mean surface-distance between MMA and ISL was 2.3 ± 0.8 mm (RS) and 2.8 ± 1.1 mm (GS). ISL and MMA volumes diverged by 5.1 ± 23.3 cc (RS) and 16.5 ± 34.1 cc (GS); the median conformity index of both structures was 0.83 (RS) and 0.80 (GS). The average relative directional errors were ≤0.7 mm (RS) and ≤0.3 mm (GS); the median absolute 3D-CoMD was 3.8 mm (RS) and 4.2 mm (GS) without statistically significant differences between the two techniques. Factors influencing the IVA included GTV and PTV (p = 0.041 and p = 0.020). Four local relapses occurred without correlation to IVA.
CONCLUSIONS
For the first time a method for IVA was presented, which can serve as a benchmarking-tool for other treatment techniques. Both techniques have shown median deviations <5 mm of planned dose and MMA. However, IVA also revealed treatments with errors ≥5 mm, suggesting a necessity for patient-specific safety-margins. Nevertheless, the treatment accuracy of well-performed active motion-compensated liver SBRT seems not to be a driving factor for local treatment failure.

Identifiants

pubmed: 31005210
pii: S0167-8140(19)30028-3
doi: 10.1016/j.radonc.2019.01.023
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

158-165

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Judit Boda-Heggemann (J)

Department of Radiation Oncology, Universitätsmedizin Mannheim, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany. Electronic address: judit.boda-heggemann@umm.de.

Anika Jahnke (A)

Department of Radiation Oncology, Universitätsmedizin Mannheim, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

Mark K H Chan (MKH)

University Medical Center Schleswig-Holstein, Department of Radiation Oncology, Kiel, Germany.

Floris Ernst (F)

University of Lübeck, Institute for Robotic and Cognitive Systems, Lübeck, Germany.

Ardekani Leila Ghaderi (AL)

University Medical Center Schleswig-Holstein, Department of Radiation Oncology, Kiel, Germany.

Ulrike Attenberger (U)

IKRN, Universitätsmedizin Mannheim, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

Peter Hunold (P)

University Medical Center Schleswig-Holstein, Department of Radiology and Nuclear Medicine, Lübeck, Germany.

Jost Philipp Schäfer (JP)

University Medical Center Schleswig-Holstein, Department of Radiology and Neuroradiology, Kiel, Germany.

Stefan Wurster (S)

Saphir Radiosurgery Center, Güstrow, Germany; University Medicine Greifswald, Ambulatory Healthcare Center, Department of Radiation Oncology, Greifswald, Germany.

Dirk Rades (D)

University Medical Center Schleswig-Holstein, Department of Radiation Oncology, Lübeck, Germany.

Guido Hildebrandt (G)

University Medicine Rostock, Department of Radiation Oncology, Rostock, Germany.

Frank Lohr (F)

UO di Radioterapia, Dipartimento di Oncologia, Azienda Ospedaliero-Universitaria di Modena, Italy.

Jürgen Dunst (J)

University Medical Center Schleswig-Holstein, Department of Radiation Oncology, Kiel, Germany.

Frederik Wenz (F)

Department of Radiation Oncology, Universitätsmedizin Mannheim, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

Oliver Blanck (O)

University Medical Center Schleswig-Holstein, Department of Radiation Oncology, Kiel, Germany; Saphir Radiosurgery Center, Güstrow, Germany.

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