Kim Myungsoo, Lee Jihae, Ha Boram, Lee Rena, Lee Kyung-Ja, Suh Hyun Suk
Department of Radiation Oncology, Ewha Womans University School of Medicine, Seoul, Korea.
Radiat Oncol J. 2011 Sep;29(3):181-90. doi: 10.3857/roj.2011.29.3.181. Epub 2011 Sep 30.
Thoracic radiotherapy is a major treatment modality of stage III non-small cell lung cancer. The normal lung tissue is sensitive to radiation and radiation pneumonitis is the most important dose-limiting complication of thoracic radiation therapy. This study was performed to identify the clinical and dosimetric parameters related to the risk of radiation pneumonitis after definitive radiotherapy in stage III non-small cell cancer patients.
The medical records were reviewed for 49 patients who completed definitive radiation therapy for locally advanced non-small cell lung cancer from August 2000 to February 2010. Radiation therapy was delivered with the daily dose of 1.8 Gy to 2.0 Gy and the total radiation dose ranged from 50.0 Gy to 70.2 Gy (median, 61.2 Gy). Elective nodal irradiation was delivered at a dose of 45.0 Gy to 50.0 Gy. Seven patients (14.3%) were treated with radiation therapy alone and forty two patients (85.7%) were treated with chemotherapy either sequentially or concurrently.
Twenty-five cases (51.0%) out of 49 cases experienced radiation pneumonitis. According to the radiation pneumonitis grade, 10 (20.4%) were grade 1, 9 (18.4%) were grade 2, 4 (8.2%) were grade 3, and 2 (4.1%) were grade 4. In the univariate analyses, no clinical factors including age, sex, performance status, smoking history, underlying lung disease, tumor location, total radiation dose and chemotherapy were associated with grade ≥2 radiation pneumonitis. In the subgroup analysis of the chemotherapy group, concurrent rather than sequential chemotherapy was significantly related to grade ≥2 radiation pneumonitis comparing sequential chemotherapy. In the univariate analysis with dosimetric factors, mean lung dose (MLD), V(20), V(30), V(40), MLDipsi, V(20)ipsi, V(30)ipsi, and V(40)ipsi were associated with grade ≥2 radiation pneumonitis. In addition, multivariate analysis showed that MLD and V30 were independent predicting factors for grade ≥2 radiation pneumonitis.
Concurrent chemotherapy, MLD and V(30) were statistically significant predictors of grade ≥2 radiation pneumonitis in patients with stage III non-small cell lung cancer undergoing definitive radiotherapy. The cutoff values for MLD and V(30) were 16 Gy and 18%, respectively.
胸部放疗是Ⅲ期非小细胞肺癌的主要治疗方式。正常肺组织对辐射敏感,放射性肺炎是胸部放疗最重要的剂量限制性并发症。本研究旨在确定Ⅲ期非小细胞癌患者根治性放疗后与放射性肺炎风险相关的临床和剂量学参数。
回顾了2000年8月至2010年2月间完成局部晚期非小细胞肺癌根治性放疗的49例患者的病历。放疗每日剂量为1.8 Gy至2.0 Gy,总辐射剂量为50.0 Gy至70.2 Gy(中位数,61.2 Gy)。选择性淋巴结照射剂量为45.0 Gy至50.0 Gy。7例患者(14.3%)仅接受放疗,42例患者(85.7%)接受序贯或同步化疗。
49例患者中有25例(51.0%)发生放射性肺炎。根据放射性肺炎分级,1级10例(20.4%),2级9例(18.4%),3级4例(8.2%),4级2例(4.1%)。单因素分析中,包括年龄、性别、体能状态、吸烟史、基础肺部疾病、肿瘤位置、总辐射剂量和化疗在内的临床因素均与≥2级放射性肺炎无关。在化疗组的亚组分析中,与序贯化疗相比,同步化疗与≥2级放射性肺炎显著相关。剂量学因素的单因素分析中,平均肺剂量(MLD)、V(20)、V(30)、V(40)、MLDipsi、V(20)ipsi、V(30)ipsi和V(40)ipsi与≥2级放射性肺炎相关。此外,多因素分析显示MLD和V30是≥2级放射性肺炎的独立预测因素。
同步化疗、MLD和V(30)是接受根治性放疗的Ⅲ期非小细胞肺癌患者≥2级放射性肺炎的统计学显著预测因素。MLD和V(30)的临界值分别为16 Gy和18%。