Literature DB >> 22560548

Evaluation of tumor shape variability in head-and-neck cancer patients over the course of radiation therapy using implanted gold markers.

Olga Hamming-Vrieze1, Simon Robert van Kranen, Suzanne van Beek, Wilma Heemsbergen, Marcel van Herk, Michiel Wilhelmus Maria van den Brekel, Jan-Jakob Sonke, Coenraad Robert Nico Rasch.   

Abstract

PURPOSE: This study quantifies tumor shape variability in head-and-neck cancer patients during radiation therapy using implanted markers. METHODS AND MATERIALS: Twenty-seven patients with oropharyngeal tumors treated with (chemo)radiation were included. Helical gold markers (0.35 × 2 mm, 3-10/patient, average 6) were implanted around the tumor. Markers were identified on planning computed tomography (CT) and daily cone beam CT (CBCT). After bony anatomy registration, the daily vector length on CBCT in reference to the planning CT and daily marker movement perpendicular to the gross tumor volume (GTV) surface at planning CT (d(normal)) of each marker were analyzed. Time trends were assessed with linear regression of the <d(normal)>(markers). In 2 patients, 2 markers were implanted in normal tissue to evaluate migration by measuring intermarker distances.
RESULTS: Marker implantation was feasible without complications. Three-dimensional vectors (4827 measurements, mean 0.23 cm, interquartile ratio 0.24 cm) were highest in base of tongue sublocalization (P<.001) and bulky tumors (vectors exceeded 0.5 cm in 5.7% [0-20 mL], 12.0% [21-40 mL], and 21.7% [≥ 41 mL], respectively [P<.001] of measurements). The measured inward time trend in 11/27 patients correlated with the visual observed marker pattern. In patients with an outward trend (5/27) or no trend (11/27), visual observation showed predominantly an inhomogeneous pattern. Remarkably, in 6 patients, outward marker movement was observed in the posterior pharyngeal wall. The difference in distance between normal tissue markers (1 SD) was 0.05-0.06 cm without time trend, indicating that implanted markers did not migrate.
CONCLUSIONS: During head-and-neck radiation therapy, normal tissue markers remained stable. Changes in position of tumor markers depended on sublocalization and tumor volume. Large differences in marker patterns between patients as well as within patients were observed. Based on our study, the cranial and caudal border in the posterior pharyngeal wall are at highest risk to be covered insufficiently. Furthermore, implanted markers could help identify patients with an actual shrinkage of the GTV who might benefit from mid-radiation therapy redelineation to reduce toxicity.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22560548     DOI: 10.1016/j.ijrobp.2012.03.014

Source DB:  PubMed          Journal:  Int J Radiat Oncol Biol Phys        ISSN: 0360-3016            Impact factor:   7.038


  8 in total

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Journal:  Strahlenther Onkol       Date:  2016-06-20       Impact factor: 3.621

3.  The tumor shape changes of nasopharyngeal cancer during chemoradiotherapy: the estimated margin to cover the geometrical variation.

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5.  Estimation of daily interfractional larynx residual setup error after isocentric alignment for head and neck radiotherapy: quality assurance implications for target volume and organs-at-risk margination using daily CT on- rails imaging.

Authors:  Charles A Baron; Musaddiq J Awan; Abdallah S R Mohamed; Imad Akel; David I Rosenthal; G Brandon Gunn; Adam S Garden; Brandon A Dyer; Laurence Court; Parag R Sevak; Esengul Kocak-Uzel; Clifton D Fuller
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Journal:  Life (Basel)       Date:  2022-02-06

7.  Accuracy quantification of a deformable image registration tool applied in a clinical setting.

Authors:  Christoph Hoffmann; Sonja Krause; Eva M Stoiber; Angela Mohr; Stefan Rieken; Oliver Schramm; Jürgen Debus; Florian Sterzing; Rolf Bendl; Kristina Giske
Journal:  J Appl Clin Med Phys       Date:  2014-01-06       Impact factor: 2.102

8.  Protocolised way to cope with anatomical changes in head & neck cancer during the course of radiotherapy.

Authors:  Suzanne van Beek; Marcel Jonker; Olga Hamming-Vrieze; Abrahim Al-Mamgani; Arash Navran; Peter Remeijer; Jeroen B van de Kamer
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  8 in total

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