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Int J Radiat Oncol Biol Phys. 2008 Dec 1;72(5):1385-95. doi: 10.1016/j.ijrobp.2008.03.007. Epub 2008 May 15.

Effects of interfractional motion and anatomic changes on proton therapy dose distribution in lung cancer.

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  • 1Department of Radiation Phyiscs, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.

Abstract

PURPOSE:

Proton doses are sensitive to intra- and interfractional anatomic changes. We analyzed the effects of interfractional anatomic changes in doses to lung tumors treated with proton therapy.

METHODS AND MATERIALS:

Weekly four-dimensional computed tomography (4D-CT) scans were acquired for 8 patients with mobile Stage III non-small cell lung cancer who were actually treated with intensity-modulated photon radiotherapy. A conformal proton therapy passive scattering plan was designed for each patient. Dose distributions were recalculated at end-inspiration and end-expiration breathing phases on each weekly 4D-CT data set using the same plans with alignment based on bone registration.

RESULTS:

Clinical target volume (CTV) coverage was compromised (from 99% to 90.9%) in 1 patient because of anatomic changes and motion pattern variation. For the rest of the patients, the mean CTV coverage on the repeated weekly 4D-CT data sets was 98.4%, compared with 99% for the original plans. For all 8 patients, however, a mean 4% increase in the volume of the contralateral lung receiving a dose of at least 5 Gy (V5) and a mean 4.4-Gy increase in the spinal cord maximum dose was observed in the repeated 4D-CT data sets. A strong correlation between the CTV density change resulting from tumor shrinkage or anatomic variations and mean contralateral lung dose was observed.

CONCLUSIONS:

Adaptive re-planning during proton therapy may be indicated in selected patients with non-small cell lung cancer. For most patients, however, CTV coverage is adequate if tumor motion is taken into consideration in the original simulation and planning processes.

PMID:
18486357
[PubMed - indexed for MEDLINE]
PMCID:
PMC3401022
Free PMC Article
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