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  4. Clinical outcomes and toxicity predictors of thoracic re-irradiation for locoregionally recurrent lung cancer
 
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Clinical outcomes and toxicity predictors of thoracic re-irradiation for locoregionally recurrent lung cancer

Journal
Clinical and Translational Radiation Oncology
Journal Volume
22
Pages
76-82
Date Issued
2020
Author(s)
WEN-CHI YANG  
FENG-MING HSU  
YU-HSUAN CHEN  
JIN-YUAN SHIH  
CHONG-JEN YU  
Lu S.-H.
ZHONG-ZHE LIN  
CHIH-HSIN YANG  
ANN-LII CHENG  
SUNG-HSIN KUO  
DOI
10.1016/j.ctro.2020.03.008
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85082684582&doi=10.1016%2fj.ctro.2020.03.008&partnerID=40&md5=1eea859ece04b2e064c9caa1300b5f8e
https://scholars.lib.ntu.edu.tw/handle/123456789/494445
Abstract
Background and purpose: Thoracic re-irradiation may be an alternative treatment for lung cancer patients who develop intrathoracic locoregional recurrence without systemic progression. This study aimed to retrospectively assess locoregional control, clinical outcomes, and toxicities in lung cancer patients who received thoracic re-irradiation. Materials and methods: We retrospectively reviewed 50 lung cancer patients who received thoracic re-irradiation using conventional photon radiotherapy (RT) and stereotactic body radiotherapy (SBRT) between 2009 and 2017. The correlations of clinicopathologic factors, treatment factors, and dosimetric factors of RT with time to local progression (TTLP), progression-free survival (PFS), and overall survival (OS) after starting thoracic re-irradiation were calculated using log-rank tests and Cox regression models. Results: The median re-irradiation dose in equivalent dose in 2-Gy fractions was 51.1 Gy, and the mean re-irradiation planning target volume was 201.58 ml. The median mean lung dose (MLD) was 4.18 Gy, and the total lung volumes receiving a dose of 5 Gy (lung V5) and of 20 Gy (V20) were 19.8% and 5.85%, respectively. The TTLP, PFS, and OS were 18.0, 5.9, and 25.1 months, respectively. Lung V5 (p < 0.001), V20 (p = 0.011), and MLD (p = 0.002) were significantly associated with grade ?2 lung toxicity. Seven (14%) patients developed lethal lung events. Subsequent chemotherapy following thoracic re-irradiation was significantly correlated with lethal lung events (p = 0.009). Conclusion: Promising local control can be achieved with thoracic re-irradiation in lung cancer patients with locoregional recurrence. However, unexpected lethal lung events may occur, especially in patients receiving systemic therapy following thoracic re-irradiation. ? 2020 The Authors
SDGs

[SDGs]SDG3

Other Subjects
aged; Article; cancer chemotherapy; cancer control; cancer growth; cancer radiotherapy; clinical article; clinical outcome; female; human; lung toxicity; male; non small cell lung cancer; overall survival; photon therapy; planning target volume; pneumonia; progression free survival; radiation dose; radiation dose distribution; radiation response; re-irradiation; retrospective study; small cell lung cancer; stereotactic body radiation therapy; total lung capacity
Publisher
Elsevier Ireland Ltd
Type
journal article

臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

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開放取用是從使用者角度提升資訊取用性的社會運動,應用在學術研究上是透過將研究著作公開供使用者自由取閱,以促進學術傳播及因應期刊訂購費用逐年攀升。同時可加速研究發展、提升研究影響力,NTU Scholars即為本校的開放取用典藏(OA Archive)平台。(點選深入了解OA)

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