Stereotactic body radiotherapy for early stage non-small cell lung cancer in patients with subclinical interstitial lung disease

被引:9
|
作者
Liu, Yuanjun [1 ,2 ]
Zhu, Yaoyao [2 ]
Wu, Ran [2 ]
Hu, Min [2 ]
Zhang, Lingnan [3 ]
Lin, Qingren [4 ]
Weng, Denghu [4 ]
Sun, Xiaojiang [4 ]
Liu, Yu [2 ]
Xu, Yaping [1 ,2 ,4 ]
机构
[1] Wenzhou Med Univ, First Clin Med Sch, Wenzhou, Peoples R China
[2] Tongji Univ, Sch Med, Dept Radiat Oncol, Shanghai Pulm Hosp, 507 Zhengmin Rd, Shanghai, Peoples R China
[3] Univ Chinese Acad Sci, Dept Radiol, Canc Hosp, Zhejiang Canc Hosp,Inst Canc & Basic Med IBMC,Chi, Hangzhou, Peoples R China
[4] Univ Chinese Acad Sci, Dept Radiat Oncol, Canc Hosp, Zhejiang Canc Hosp,Inst Canc & Basic Med IBMC,Chi, Hangzhou, Peoples R China
关键词
Non-small cell lung cancer (NSCLC); outcome; stereotactic body radiotherapy (SBRT); toxicity; subclinical interstitial lung disease; IDIOPATHIC PULMONARY-FIBROSIS; RADIATION PNEUMONITIS; ACUTE EXACERBATION; THERAPY;
D O I
10.21037/tlcr-20-1050
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: For lung cancer patients with subclinical (untreated and asymptomatic) interstitial lung disease (ILD), there is a lack of relatively safe and effective treatment. Stereotactic body radiation therapy (SBRT) can achieve a high level of tumor control with low toxicity in early-stage non-small cell lung cancer (NSCLC). This study aimed to evaluate the efficacy and toxicity of early stage NSCLC patients with subclinical ILD receiving SBRT. Methods: A total of 109 early stage NSCLC patients receiving SBRT treatment between December 2011 and August 2016 were reviewed in our institutions; patients with clinical ILD were excluded. The median dose of SBRT was 50 Gy in 5 fractions. The median biologically effective dose (BED; alpha/beta=10) was 100 Gy (range, 72-119 Gy). An experienced radiation oncologist and an experienced radiologist reviewed the presence of subclinical ILD in the CT findings before SBRT. The relationships among the efficacy, radiation-induced lung injury (RILI) and subclinical ILD were explored. Results: In all, 38 (34.9%) of 109 patients were recognized with subclinical ILD before SBRT, 48 (44.0%) of 109 patients were recognized with grade 2-5 RILI after SBRT, and 18 (47.4%) of 38 patients with subclinical ILD were observed with grade 2-5 RILI. Subclinical ILD was not a significant factor of grade 2-5 RILI (P=0.608); however, 3 patients had extensive RILI, and they all suffered from subclinical ILD. Dosimetric factor of the lungs, such as mean lung dose (MLD) was significantly related with Grade 2-5 RILI in patients with subclinical ILD (P=0.042). The progression-free survival (PFS) rates at 3 years in the subclinical ILD patients and those without ILD were 61.6% and 66.8%, respectively (P=0.266). Conclusions: Subclinical ILD was not a significant factor for RILI or PFS in early stage NSCLC patients receiving SBRT; however, patients with subclinical ILD receiving SBRT may experience uncommon extensive RILI.
引用
收藏
页码:2328 / 2336
页数:10
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