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A comparison of the incidence of ≥ grade 2 radiation pneumonitis between intensity-modulated radiotherapy and three-dimensional conformal radiotherapy in patients with unresectable non-small cell lung cancer treated with durvalumab after concurrent chemoradiotherapy

医学 放射治疗 杜瓦卢马布 肺炎 危险系数 放化疗 肺癌 回顾性队列研究 核医学 入射(几何) 置信区间 放射科 内科学 癌症 物理 免疫疗法 光学 无容量
作者
Masahiro Masuo,Eiko Shinohara,Masataka Kitano,Ryusuke Maruta,Satoshi Chonabayashi,Shun Endo,Suhei Matumoto,Naoki Nishiyama,Yumiko Machitori,Masayoshi Kobayashi
出处
期刊:Japanese Journal of Clinical Oncology [Oxford University Press]
卷期号:54 (3): 312-318 被引量:3
标识
DOI:10.1093/jjco/hyad158
摘要

Abstract Background Intensity-modulated radiation therapy (IMRT) has been increasingly used as a new radiation modality for unresectable non-small cell lung cancer (NSCLC). The risk factors for radiation pneumonitis (RP) during consolidation durvalumab following concurrent chemoradiotherapy (CCRT) using IMRT have not been thoroughly investigated. Methods This retrospective study analyzed medical record data from consecutive patients diagnosed with NSCLC who underwent CCRT and consolidation durvalumab at our institution between April 2018 and September 2022. Since we adopted IMRT for the treatment of NSCLC in April 2020, these patients were categorized into two groups: those treated with IMRT after April 2020 and those treated with three-dimensional conformal radiotherapy (3D-CRT) before April 2020. Results A total of 31 patients underwent IMRT (the IMRT group), while 25 patients underwent 3D-CRT (the 3D-CRT group). In both groups, the total dose was 60 Gy in 30 fractions. The cumulative incidence of ≥ grade 2 RP at 12 months was significantly lower in the IMRT group than in the 3D-CRT group (27.0% vs. 64.0%, hazard ratio [HR]: 0.338, 95% confidence interval [CI]: 0.144–0.793, p = 0.013). In the multivariable analysis, V20 (≥ 25.6%, HR: 2.706, 95% CI: 1.168–6.269, p = 0.020) and radiotherapy technique (IMRT, HR: 0.414, 95% CI: 0.172–0.994, p = 0.048) were identified as significant risk factors for ≥ grade 2 RP. Conclusions IMRT is associated with a lower rate of ≥ grade 2 RP in patients with NSCLC who received CCRT followed by durvalumab.

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