Quantifying variability of intrafractional target motion in stereotactic body radiotherapy for lung cancers
| Autor: | Sherry C.Y. Ng, Eric W C Tam, Mark K.H. Chan, Dora L.W. Kwong, Anthony S. M. Tong |
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| Rok vydání: | 2013 |
| Předmět: |
Organs at Risk
Lung Neoplasms Movement medicine.medical_treatment Radiosurgery Motion (physics) Organ Motion Cyberknife medicine Humans Radiation Oncology Physics intrafractional variation of tumor motion Radiology Nuclear Medicine and imaging Four-Dimensional Computed Tomography Radiation treatment planning Instrumentation Physics Reproducibility Radiation business.industry Radiotherapy Planning Computer-Assisted Radiotherapy Dosage Tumor Burden Amplitude stereotactic body radiotherapy Nuclear medicine business Algorithms |
| Zdroj: | Journal of Applied Clinical Medical Physics |
| ISSN: | 1526-9914 |
| DOI: | 10.1120/jacmp.v14i5.4319 |
| Popis: | In lung stereotactic body radiotherapy (SBRT), variability of intrafractional target motion can negate the potential benefits of four‐dimensional (4D) treatment planning that aims to account for the dosimetric impacts of organ motion. This study used tumor motion data obtained from CyberKnife SBRT treatments to quantify the reproducibility of probability motion function (pmf) of 37 lung tumors. The reproducibility of pmf was analyzed with and without subtracting the intrafractional baseline drift from the original motion data. Statistics of intrafractional tumor motion including baseline drift, target motion amplitude and period, were also calculated. The target motion amplitude significantly correlates with variations (1 SD) of motion amplitude and baseline drift. Significant correlation between treatment time and variations (1 SD) of motion amplitude was observed in anterior‐posterior (AP) motion, but not in craniocaudal (CC) and left‐right (LR) motion. The magnitude of AP and LR baseline drifts significantly depend on the treatment time, while the CC baseline drift does not. The reproducibility of pmf as a function of time can be well described by a two‐exponential function with a fast and slow component. The reproducibility of pmf is over 60% for the CC motion and over 50% for the AP and LR motions when baseline variations were subtracted from the original motion data. It decreases to just over 30% for the CC motion and about 20% for the AP and LR motion, otherwise. 4D planning has obvious limitations due to variability of intrafractional target motion. To account for potential risks of overdosing critical organs, it is important to simulate the dosimetric impacts of intra‐ and interfractional baseline drift using population statistics obtained from SBRT treatments. PACS number: 87.55.‐x |
| Databáze: | OpenAIRE |
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