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Intensity-modulated radiation therapy with concurrent chemotherapy followed by durvalumab for stage III non-small cell lung cancer: A multi-center retrospective study

杜瓦卢马布 医学 肺炎 放射治疗 肿瘤科 内科学 放化疗 回顾性队列研究 阶段(地层学) 肺癌 多元分析 入射(几何) 癌症 无容量 免疫疗法 古生物学 物理 光学 生物
作者
Yoko Tsukita,Takaya Yamamoto,Hiroshi Mayahara,Akito Hata,Yuichiro Takeda,Hidetsugu Nakayama,Satoshi Tanaka,Junji Uchida,Kazuhiro Usui,Tatsuya Toyoda,Motohiro Tamiya,Masahiro Morimoto,Yuko Oya,Takeshi Kodaira,Eisaku Miyauchi,Keiichi Jingu,Hisatoshi Sugiura
出处
期刊:Radiotherapy and Oncology [Elsevier BV]
卷期号:160: 266-272 被引量:29
标识
DOI:10.1016/j.radonc.2021.05.016
摘要

Abstract Background and purpose Intensity-modulated radiation therapy (IMRT) is increasingly applied in concurrent chemoradiotherapy (CCRT) for locally-advanced non-small cell lung cancer (NSCLC), with improvement of target coverage and better sparing of normal tissue. IMRT tends to have a larger low-dose irradiation volume than 3D conformal radiotherapy, but the incidence of and risk factors for pneumonitis remain unclear, especially following the approval of durvalumab. Materials and methods We retrospectively reviewed the records of NSCLC patients treated by CCRT using IMRT at seven Japanese institutions. Primary outcomes were incidence of symptomatic pneumonitis and progression-free survival (PFS). Multivariate logistic regression analysis was used to identify risk factors for ≥grade 2 pneumonitis. Results Median follow-up from the start of CCRT was 14.3 months (n = 107 patients; median age 70 years, 29% female). Median lung V5 and V20 was 49.2% and 19.5%, respectively. Durvalumab was administered to 87 patients (81%). Pneumonitis developed in 95 (89%) patients of which 53% had grade 1, 28% grade 2, 6.5% grade 3, and 0.9% grade 4. Durvalumab had been discontinued in 16 patients (18.4%) due to pneumonitis. By multivariate analysis, age ≥70 years, male sex, and V5 ≥58.9% were identified as significantly associated with ≥grade 2 pneumonitis (p = 0.0065, 0.036 and 0.0013 respectively). The median PFS from the start of CCRT was not reached (95% CI, 14.2 months to not reached) in patients receiving durvalumab. Conclusion CCRT using IMRT followed by durvalumab was generally effective and tolerable; V5
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