7-Year Follow-Up After Stereotactic Ablative Radiotherapy for Patients With Stage I Non-Small Cell Lung Cancer: Results of a Phase 2 Clinical Trial

被引:129
作者
Sun, Bing [1 ,5 ]
Brooks, Eric D. [1 ]
Komaki, Ritsuko U. [1 ]
Liao, Zhongxing [1 ]
Jeter, Melenda D. [1 ]
McAleer, Mary F. [1 ]
Allen, Pamela K. [1 ]
Balter, Peter A. [2 ]
Welsh, James D. [1 ]
O'Reilly, Michael S. [1 ]
Gomez, Daniel [1 ]
Hahn, Stephen M. [1 ]
Roth, Jack A. [3 ]
Mehran, Reza J. [3 ]
Heymach, John V. [4 ]
Chang, Joe Y. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Radiat Oncol, 1515 Holcombe Blvd, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Radiat Phys, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Thorac & Cardiovasc Surg, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
[5] Acad Mil Med Sci, Affiliated Hosp, Dept Radiat Oncol, Beijing, Peoples R China
基金
美国国家卫生研究院;
关键词
non-small cell lung cancer (NSCLC); patterns of failure; stage I disease; stereotactic ablative radiotherapy (SABR); stereotactic body radiotherapy; BODY RADIATION-THERAPY; ASSISTED THORACOSCOPIC SURGERY; PROPENSITY-MATCHED ANALYSIS; DISEASE RECURRENCE; RESECTION; LOBECTOMY; PATTERNS; SURVIVAL; OUTCOMES; MULTICENTER;
D O I
10.1002/cncr.30693
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: The authors evaluated the efficacy, patterns of failure, and toxicity of stereotactic ablative radiotherapy (SABR) for patients with medically inoperable, clinical stage I non-small cell lung cancer (NSCLC) in a prospective clinical trial with 7 years of follow-up. Clinical staging was performed according to the seventh edition of the American Joint Committee on Cancer TNM staging system. METHODS: Eligible patients with histologically confirmed NSCLC of clinical stage I as determined using positron emission tomography staging were treated with SABR (50 grays in 4 fractions). The primary endpoint was progression-free survival. Patients were followed with computed tomography and/or positron emission tomography/computed tomography every 3 months for the first 2 years, every 6 months for the next 3 years, and then annually thereafter. RESULTS: A total of 65 patients were eligible for analysis. The median age of the patients was 71 years, and the median follow-up was 7.2 years. A total of 18 patients (27.7%) developed disease recurrence at a median of 14.5 months (range, 4.3-71.5 months) after SABR. Estimated incidences of local, regional, and distant disease recurrence using competing risk analysis were 8.1%, 10.9%, and 11.0%, respectively, at 5 years and 8.1%, 13.6%, and 13.8%, respectively, at 7 years. A second primary lung carcinoma developed in 12 patients (18.5%) at a median of 35 months (range, 5-67 months) after SABR. Estimated 5-year and 7-year progression-free survival rates were 49.5% and 38.2%, respectively; the corresponding overall survival rates were 55.7% and 47.5%, respectively. Three patients (4.6%) experienced grade 3 treatment-related adverse events. No patients developed grade 4 or 5 adverse events (toxicity was graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events [version 3.0]). CONCLUSIONS: With long-term follow-up, the results of the current prospective study demonstrated outstanding local control and low toxicity after SABR in patients with clinical stage I NSCLC. Regional disease recurrence and distant metastases were the dominant manifestations of failure. Surveillance for second primary lung carcinoma is recommended. (C) 2017 American Cancer Society.
引用
收藏
页码:3031 / 3039
页数:9
相关论文
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