Radiation pneumonitis after definitive concurrent chemoradiotherapy with cisplatin/docetaxel for non‐small cell lung cancer: Analysis of dose‐volume parameters

Abstract Background Radiation pneumonitis (RP) is a major pulmonary adverse event of chest radiotherapy. The PACIFIC trial that identified durvalumab as an effective subsequent‐line therapy after concurrent chemoradiotherapy (CCRT) found that patients with grade 2 or higher RP may have to be exclude...

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Main Authors: Kuniaki Katsui, Takeshi Ogata, Kenta Watanabe, Norihisa Katayama, Masahiro Kuroda, Katsuyuki Kiura, Takao Hiraki, Yoshinobu Maeda, Shinichi Toyooka, Susumu Kanazawa
Format: Article
Language:English
Published: Wiley 2020-07-01
Series:Cancer Medicine
Subjects:
Online Access:https://doi.org/10.1002/cam4.3093
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spelling doaj-1311f4b5f643477bb60027f1b24c8d3c2020-11-25T02:38:10ZengWileyCancer Medicine2045-76342020-07-019134540454910.1002/cam4.3093Radiation pneumonitis after definitive concurrent chemoradiotherapy with cisplatin/docetaxel for non‐small cell lung cancer: Analysis of dose‐volume parametersKuniaki Katsui0Takeshi Ogata1Kenta Watanabe2Norihisa Katayama3Masahiro Kuroda4Katsuyuki Kiura5Takao Hiraki6Yoshinobu Maeda7Shinichi Toyooka8Susumu Kanazawa9Department of Proton Beam Therapy Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science Okayama JapanDepartment of Radiology Iwakuni Clinical Center Yamaguchi JapanDepartment of Radiology Okayama University Hospital Okayama JapanDepartment of Radiology Okayama University Hospital Okayama JapanDepartment of Radiological Technology Graduate School of Health Sciences Okayama University Okayama JapanDepartment of Allergy and Respiratory Medicine Okayama University Hospital Okayama JapanDepartment of Radiology Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science Okayama JapanDepartment of Hematology, Oncology, and Respiratory Medicine Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science Okayama JapanDepartments of General Thoracic Surgery and Breast and Endocrinological Surgery Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science Okayama JapanDepartment of Radiology Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science Okayama JapanAbstract Background Radiation pneumonitis (RP) is a major pulmonary adverse event of chest radiotherapy. The PACIFIC trial that identified durvalumab as an effective subsequent‐line therapy after concurrent chemoradiotherapy (CCRT) found that patients with grade 2 or higher RP may have to be excluded from treatment under certain criteria. The purpose of this study was to investigate the relationship between grade ≥2 RP and the parameters of dose‐volume histograms after CCRT with cisplatin/docetaxel for stage III non‐small cell lung cancer and conduct a subset analysis of severe RP that can lead to the permanent discontinuation of treatment per the PACIFIC trial criteria to help determine treatment strategy. Methods We calculated the percentage of the lung volume received at least 5 Gy (V5) and 20 Gy (V20), the mean lung dose (MLD), and the lung volume spared from a 5 Gy dose (VS5) to the total lung volume. Factors affecting the incidence of grade ≥2 RP were identified; severe RP was defined as grade ≥3 as well as grade 2 RP that required ≥10 mg prednisolone for at least 12 weeks. Results This study included 45 patients. On univariate analysis, all parameters and total lung volume were found to be significant predictors of grade ≥2 RP (P = .001, .003, .03, .004, and .02, respectively). On multivariate analysis, V20 was a significant predictive factor of grade ≥2 RP (P = .007). Severe RP developed in 6 of 37 patients (16.2%) whose V20 values were 35% or lower. On univariate analysis, only V20 was a significant predictor of severe RP in these patients (P = .01). Conclusions The best approach to reduce the rate of grade ≥2 RP is to maintain the V5, V20, MLD, and VS5 as low as possible during radiotherapy planning in patients receiving definitive CCRT with cisplatin/docetaxel.https://doi.org/10.1002/cam4.3093cisplatin/docetaxeldose‐volume histogramnon‐small cell lung cancerPACIFIC trialradiation pneumonitis
collection DOAJ
language English
format Article
sources DOAJ
author Kuniaki Katsui
Takeshi Ogata
Kenta Watanabe
Norihisa Katayama
Masahiro Kuroda
Katsuyuki Kiura
Takao Hiraki
Yoshinobu Maeda
Shinichi Toyooka
Susumu Kanazawa
spellingShingle Kuniaki Katsui
Takeshi Ogata
Kenta Watanabe
Norihisa Katayama
Masahiro Kuroda
Katsuyuki Kiura
Takao Hiraki
Yoshinobu Maeda
Shinichi Toyooka
Susumu Kanazawa
Radiation pneumonitis after definitive concurrent chemoradiotherapy with cisplatin/docetaxel for non‐small cell lung cancer: Analysis of dose‐volume parameters
Cancer Medicine
cisplatin/docetaxel
dose‐volume histogram
non‐small cell lung cancer
PACIFIC trial
radiation pneumonitis
author_facet Kuniaki Katsui
Takeshi Ogata
Kenta Watanabe
Norihisa Katayama
Masahiro Kuroda
Katsuyuki Kiura
Takao Hiraki
Yoshinobu Maeda
Shinichi Toyooka
Susumu Kanazawa
author_sort Kuniaki Katsui
title Radiation pneumonitis after definitive concurrent chemoradiotherapy with cisplatin/docetaxel for non‐small cell lung cancer: Analysis of dose‐volume parameters
title_short Radiation pneumonitis after definitive concurrent chemoradiotherapy with cisplatin/docetaxel for non‐small cell lung cancer: Analysis of dose‐volume parameters
title_full Radiation pneumonitis after definitive concurrent chemoradiotherapy with cisplatin/docetaxel for non‐small cell lung cancer: Analysis of dose‐volume parameters
title_fullStr Radiation pneumonitis after definitive concurrent chemoradiotherapy with cisplatin/docetaxel for non‐small cell lung cancer: Analysis of dose‐volume parameters
title_full_unstemmed Radiation pneumonitis after definitive concurrent chemoradiotherapy with cisplatin/docetaxel for non‐small cell lung cancer: Analysis of dose‐volume parameters
title_sort radiation pneumonitis after definitive concurrent chemoradiotherapy with cisplatin/docetaxel for non‐small cell lung cancer: analysis of dose‐volume parameters
publisher Wiley
series Cancer Medicine
issn 2045-7634
publishDate 2020-07-01
description Abstract Background Radiation pneumonitis (RP) is a major pulmonary adverse event of chest radiotherapy. The PACIFIC trial that identified durvalumab as an effective subsequent‐line therapy after concurrent chemoradiotherapy (CCRT) found that patients with grade 2 or higher RP may have to be excluded from treatment under certain criteria. The purpose of this study was to investigate the relationship between grade ≥2 RP and the parameters of dose‐volume histograms after CCRT with cisplatin/docetaxel for stage III non‐small cell lung cancer and conduct a subset analysis of severe RP that can lead to the permanent discontinuation of treatment per the PACIFIC trial criteria to help determine treatment strategy. Methods We calculated the percentage of the lung volume received at least 5 Gy (V5) and 20 Gy (V20), the mean lung dose (MLD), and the lung volume spared from a 5 Gy dose (VS5) to the total lung volume. Factors affecting the incidence of grade ≥2 RP were identified; severe RP was defined as grade ≥3 as well as grade 2 RP that required ≥10 mg prednisolone for at least 12 weeks. Results This study included 45 patients. On univariate analysis, all parameters and total lung volume were found to be significant predictors of grade ≥2 RP (P = .001, .003, .03, .004, and .02, respectively). On multivariate analysis, V20 was a significant predictive factor of grade ≥2 RP (P = .007). Severe RP developed in 6 of 37 patients (16.2%) whose V20 values were 35% or lower. On univariate analysis, only V20 was a significant predictor of severe RP in these patients (P = .01). Conclusions The best approach to reduce the rate of grade ≥2 RP is to maintain the V5, V20, MLD, and VS5 as low as possible during radiotherapy planning in patients receiving definitive CCRT with cisplatin/docetaxel.
topic cisplatin/docetaxel
dose‐volume histogram
non‐small cell lung cancer
PACIFIC trial
radiation pneumonitis
url https://doi.org/10.1002/cam4.3093
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