Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/32230
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    Title: Evaluating the optimal radiation dose for definitive chemoradiotherapy for esophageal squamous cell carcinoma A single institution experience
    Authors: Ke, Te-Min
    Fong, Yao
    Lin, Li-Ching
    Chien, Yu-Wun
    Yang, Ching-Chieh
    Lin, Chia-Hui
    Lin, Kuei-Li
    Que, Jenny
    Contributors: Chi Mei Med Ctr, Dept Radiat Oncol
    Chi Mei Med Ctr, Dept Thorac Surg
    Chung Hwa Univ Med Technol, Dept Optometry
    Taipei Med Univ, Sch Med
    Natl Cheng Kung Univ, Coll Med, Natl Cheng Kung Univ Hosp, Dept Publ Hlth
    Natl Cheng Kung Univ, Coll Med, Natl Cheng Kung Univ Hosp, Dept Occupat & Environm Med
    Chia Nan Univ Pharm & Sci, Dept Pharm
    Chia Nan Univ Pharm & Sci, Dept Hosp & Hlth Care Adm
    Keywords: chemoradiotherapy
    esophageal squamous cell carcinoma
    radiation dose
    Date: 2018-11
    Issue Date: 2019-11-15 15:46:01 (UTC+8)
    Publisher: LIPPINCOTT WILLIAMS & WILKINS
    Abstract: The optimal radiation dose for definitive chemoradiotherapy in inoperable esophageal squamous cell carcinoma (ESCC) has been long debated. In this study, we evaluated the effect of doses greater than the conventional radiation dose (50.4 Gy) on tumor control, tumor response, overall survival (OS), and disease-free survival (DFS). The database of patients diagnosed with inoperable ESCC from 2007 to 2015 was obtained from the cancer registry of Chi-Mei Medical Center. All categorical variables were compared using Chi-squared test. The risk of OS and DFS were estimated using Cox proportional hazards regression, and Kaplan-Meier plots presented the trend of OS and DFS with log-rank tests used to compare differences. All significance levels were set at P<.05. A total of 84 patients were retrospectively analyzed, with 42 (50%) receiving > 50.4 Gy and 42 (50%) receiving <= 50.4 Gy (50%) concurrently with chemotherapy. Univariate and multivariate analysis revealed no significant differences between higher dose and conventional dose in OS (P=.21) and DFS (P=.26). Further dose analysis of < 50, 50 to 50.4, 51 to 60, and > 60 Gy showed no significant differences in OS or DFS. Higher doses conveyed no significant benefit on the failure pattern, either local regional failure or distant failure (P=.42). Major prognostic factors associated with better OS on multivariate analysis were stages I and II patients (P=.03) and radiation technique using arc therapy (P=.04). No acute toxicity of grade III or higher was recorded. The results of our study show that providing higher than conventional radiation doses concurrent with chemotherapy for inoperable ESCC does not impact OS or DSF, nor does it improve locoregional failure or distant failure. Although tumor response might be improved by radiation doses > 50.4 Gy, the impact on OS and DFS remain to be studied.
    ???metadata.dc.relation.uri???: http://dx.doi.org/10.1097/MD.0000000000013214
    Relation: Medicine, v.97, n.46, e13214
    Appears in Collections:[Dept. of Pharmacy] Periodical Articles
    [Dept. of Hospital and Health (including master's program)] Periodical Articles

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