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      Dosimetric Effects of the Interfraction Variations during Whole Breast Radiotherapy: A Prospective Study

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          Abstract

          Introduction

          The aim of this work was to assess the dosimetric impact of the interfraction variations during breast radiotherapy.

          Materials and methods

          Daily portal imaging measurements were prospectively performed in 10 patients treated with adjuvant whole breast irradiation (50 Gy/25 fractions). Margins between the clinical target volume and the planning target volume (PTV) were 5 mm in the three dimensions. Parameters of interest were the central lung distance (CLD) and the inferior central margin (ICM). Daily movements were applied to the baseline treatment planning (TP1) to design a further TP (TP2). The PTV coverage and organ at risk exposure were measured on both TP1 and TP2, before being compared.

          Results

          A total of 241 portal images were analyzed. The random and systematic errors were 2.6 and 3.7 mm for the CLD, 4.3 and 6.9 mm for the ICM, respectively. No significant consequence on the PTV treatments was observed (mean variations: +0.1%, p = 0.56 and −1.8%, p = 0.08 for the breast and the tumor bed, respectively). The ipsilateral lung and heart exposure was not significantly modified.

          Conclusion

          In our series, the daily interfraction variations had no significant effect on the PTV coverage or healthy tissue exposure during breast radiotherapy.

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          Most cited references35

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          Breast patient setup error assessment: comparison of electronic portal image devices and cone-beam computed tomography matching results.

          To quantify the differences in setup errors measured with the cone-beam computed tomography (CBCT) and electronic portal image devices (EPID) in breast cancer patients. Repeat CBCT scan were acquired for routine offline setup verification in 20 breast cancer patients. During the CBCT imaging fractions, EPID images of the treatment beams were recorded. Registrations of the bony anatomy for CBCT to planning CT and EPID to digitally reconstructed-radiographs (DRRs) were compared. In addition, similar measurements of an anthropomorphic thorax phantom were acquired. Bland-Altman and linear regression analysis were performed for clinical and phantom registrations. Systematic and random setup errors were quantified for CBCT and EPID-driven correction protocols in the EPID coordinate system (U, V), with V parallel to the cranial-caudal axis and U perpendicular to V and the central beam axis. Bland-Altman analysis of clinical EPID and CBCT registrations yielded 4 to 6-mm limits of agreement, indicating that both methods were not compatible. The EPID-based setup errors were smaller than the CBCT-based setup errors. Phantom measurements showed that CBCT accurately measures setup error whereas EPID underestimates setup errors in the cranial-caudal direction. In the clinical measurements, the residual bony anatomy setup errors after offline CBCT-based corrections were Σ(U) = 1.4 mm, Σ(V) = 1.7 mm, and σ(U) = 2.6 mm, σ(V) = 3.1 mm. Residual setup errors of EPID driven corrections corrected for underestimation were estimated at Σ(U) = 2.2mm, Σ(V) = 3.3 mm, and σ(U) = 2.9 mm, σ(V) = 2.9 mm. EPID registration underestimated the actual bony anatomy setup error in breast cancer patients by 20% to 50%. Using CBCT decreased setup uncertainties significantly. Copyright © 2010 Elsevier Inc. All rights reserved.
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            Quantifying the effect of intrafraction motion during breast IMRT planning and dose delivery.

            Respiratory motion during intensity modulated radiation therapy (IMRT) causes two types of problems. First, the clinical target volume (CTV) to planning target volume (PTV) margin needed to account for respiratory motion means that the lung and heart dose is higher than would occur in the absence of such motion. Second, because respiratory motion is not synchronized with multileaf collimator (MLC) motion, the delivered dose is not the same as the planned dose. The aims of this work were to evaluate these problems to determine (a) the effects of respiratory motion and setup error during breast IMRT treatment planning, (b) the effects of the interplay between respiratory motion and multileaf collimator (MLC) motion during breast IMRT delivery, and (c) the potential benefits of breast IMRT using breath-hold, respiratory gated, and 4D techniques. Seven early stage breast cancer patient data sets were planned for IMRT delivered with a dynamic MLC (DMLC). For each patient case, eight IMRT plans with varying respiratory motion magnitudes and setup errors (and hence CTV to PTV margins) were created. The effects of respiratory motion and setup error on the treatment plan were determined by comparing the eight dose distributions. For each fraction of these plans, the effect of the interplay between respiratory motion and MLC motion during IMRT delivery was simulated by superimposing the respiratory trace on the planned DMLC leaf motion, facilitating comparisons between the planned and expected dose distributions. When considering respiratory motion in the CTV-PTV expansion during breast IMRT planning, our results show that PTV dose heterogeneity increases with respiratory motion. Lung and heart doses also increase with respiratory motion. Due to the interplay between respiratory motion and MLC motion during IMRT delivery, the planned and expected dose distributions differ. This difference increases with respiratory motion. The expected dose varies from fraction to fraction. However, for the seven patients studied and respiratory trace used, for no breathing, shallow breathing, and normal breathing, there were no statistically significant differences between the planned and expected dose distributions. Thus, for breast IMRT, intrafraction motion degrades treatment plans predominantly by the necessary addition of a larger CTV to PTV margin than would be required in the absence of such motion. This motion can be limited by breath-hold, respiratory gated, or 4D techniques.
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              Effects of setup errors and shape changes on breast radiotherapy.

              The purpose of the present study was to quantify the robustness of the dose distributions from three whole-breast radiotherapy (RT) techniques involving different levels of intensity modulation against whole patient setup inaccuracies and breast shape changes. For 19 patients (one computed tomography scan and five cone beam computed tomography scans each), three treatment plans were made (wedge, simple intensity-modulated RT [IMRT], and full IMRT). For each treatment plan, four dose distributions were calculated. The first dose distribution was the original plan. The other three included the effects of patient setup errors (rigid displacement of the bony anatomy) or breast errors (e.g., rotations and shape changes of the breast with respect to the bony anatomy), or both, and were obtained through deformable image registration and dose accumulation. Subsequently, the effects of the plan type and error sources on target volume coverage, mean lung dose, and excess dose were determined. Systematic errors of 1-2 mm and random errors of 2-3 mm (standard deviation) were observed for both patient- and breast-related errors. Planning techniques involving glancing fields (wedge and simple IMRT) were primarily affected by patient errors (∼6% loss of coverage near the dorsal field edge and ∼2% near the skin). In contrast, plan deterioration due to breast errors was primarily observed in planning techniques without glancing fields (full IMRT, ∼2% loss of coverage near the dorsal field edge and ∼4% near the skin). The influences of patient and breast errors on the dose distributions are comparable in magnitude for whole breast RT plans, including glancing open fields, rendering simple IMRT the preferred technique. Dose distributions from planning techniques without glancing open fields were more seriously affected by shape changes of the breast, demanding specific attention in partial breast planning techniques. Copyright © 2011 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                Journal
                Front Oncol
                Front Oncol
                Front. Oncol.
                Frontiers in Oncology
                Frontiers Media S.A.
                2234-943X
                16 September 2015
                2015
                : 5
                : 199
                Affiliations
                [1] 1Department of Radiotherapy, Gustave Roussy , Villejuif, France
                [2] 2Department of Biostatistics and Epidemiology, Gustave Roussy , Villejuif, France
                [3] 3University Paris-Sud , Kremlin-Bicêtre, France
                [4] 4Department of Physics, Gustave Roussy , Villejuif, France
                [5] 5Department of Oncologic Radiotherapy, Institut du Cancer de Montpellier , Montpellier, France
                Author notes

                Edited by: Jijo Paul, Medical College of Wisconsin, USA

                Reviewed by: Radka Stoyanova, University of Miami, USA; Sonali Rudra, Medstar Georgetown University Hospital, USA

                *Correspondence: Julian Jacob, Department of Radiotherapy, Gustave Roussy, 114 rue Edouard Vaillant, Villejuif Cedex 94 805, France, julian.jacob28@ 123456gmail.com

                Specialty section: This article was submitted to Radiation Oncology, a section of the journal Frontiers in Oncology

                Article
                10.3389/fonc.2015.00199
                4584980
                4cbdf377-1a9c-4819-a123-864b153ed882
                Copyright © 2015 Jacob, Heymann, Borget, Dumas, Riahi, Maroun, Ezra, Roberti, Rivera, Deutsch and Bourgier.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 25 May 2015
                : 31 August 2015
                Page count
                Figures: 1, Tables: 4, Equations: 0, References: 38, Pages: 7, Words: 5666
                Categories
                Oncology
                Original Research

                Oncology & Radiotherapy
                dosimetry,interfraction variations,breast radiotherapy,central lung distance,inferior central margin

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