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Intensity-modulated proton therapy for elective nodal irradiation and involved-field radiation in the definitive treatment of locally advanced non-small-cell lung cancer: a dosimetric study.

Authors :
Kesarwala AH
Ko CJ
Ning H
Xanthopoulos E
Haglund KE
O'Meara WP
Simone CB 2nd
Rengan R
Source :
Clinical lung cancer [Clin Lung Cancer] 2015 May; Vol. 16 (3), pp. 237-44. Date of Electronic Publication: 2014 Dec 09.
Publication Year :
2015

Abstract

Background: Photon involved-field (IF) radiation therapy (IFRT), the standard for locally advanced (LA) non-small cell lung cancer (NSCLC), results in favorable outcomes without increased isolated nodal failures, perhaps from scattered dose to elective nodal stations. Because of the high conformality of intensity-modulated proton therapy (IMPT), proton IFRT could increase nodal failures. We investigated the feasibility of IMPT for elective nodal irradiation (ENI) in LA-NSCLC.<br />Patients and Methods: IMPT IFRT plans were generated to the same total dose of 66.6-72 Gy received by 20 LA-NSCLC patients treated with photon IFRT. IMPT ENI plans were generated to 46 cobalt Gray equivalent (CGE) to elective nodal planning treatment volumes (PTV) plus 24 CGE to IF-PTVs.<br />Results: Proton IFRT and ENI improved the IF-PTV percentage of volume receiving 95% of the prescribed dose (D95) by 4% (P < .01) compared with photon IFRT. All evaluated dosimetric parameters improved significantly with both proton plans. The lung percentage of volume receiving 20 Gy/CGE (V20) and mean lung dose decreased 18% (P < .01) and 36% (P < .01), respectively, with proton IFRT, and 11% (P = .03) and 26% (P < .01) with ENI. The mean esophagus dose decreased 16% with IFRT and 12% with ENI; heart V25 decreased 63% with both (all P < .01).<br />Conclusion: This study demonstrates the feasibility of IMPT for LA-NSCLC ENI. Potential decreased toxicity indicates that IMPT could allow ENI while maintaining a favorable therapeutic ratio compared with photon IFRT.<br /> (Published by Elsevier Inc.)

Details

Language :
English
ISSN :
1938-0690
Volume :
16
Issue :
3
Database :
MEDLINE
Journal :
Clinical lung cancer
Publication Type :
Academic Journal
Accession number :
25604729
Full Text :
https://doi.org/10.1016/j.cllc.2014.12.001