Stereotactic Ablative Radiotherapy for stage I histologically proven non-small cell lung cancer: An Italian multicenter observational study

被引:66
作者
Ricardi, Umberto [1 ]
Frezza, Giovanni [2 ]
Filippi, Andrea Riccardo [1 ]
Badellino, Serena [1 ]
Levis, Mario [1 ]
Navarria, Piera [3 ]
Salvi, Fabrizio [2 ]
Marcenaro, Michela [4 ]
Trovo, Marco [5 ]
Guarneri, Alessia [1 ]
Corvo, Renzo [4 ]
Scorsetti, Marta [3 ]
机构
[1] Univ Turin, Dept Oncol, I-10126 Turin, Italy
[2] Bellaria Hosp, I-40139 Bologna, Italy
[3] Humanitas Canc Ctr, Radiotherapy & Radiosurgely Unit, I-20089 Rozzano, Italy
[4] Univ Genoa, Inst Canc Res & Treatment IST, I-16132 Genoa, Italy
[5] Inst Canc Res & Treatment CRO, I-33081 Aviano, Italy
关键词
Stereotactic ablative radiotherapy; Stereotactic body radiotherapy; Early stage; Non-small cell lung cancer; Radiotherapy; Lung cancer; BODY RADIATION-THERAPY; PHASE-II; PATTERNS; OUTCOMES; SURGERY; IMPACT; CARE;
D O I
10.1016/j.lungcan.2014.02.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: Aim of this retrospective multicenter observational study was to provide data on outcomes and prognostic factors in patients affected with stage I histologically confirmed NSCLC treated with Stereotactic Ablative Radiotherapy (SABR, or Stereotactic Body Radiotherapy, SBRT) outside clinical trials. Materials and Methods: We analyzed a cohort of 196 patients with histological/cytological diagnosis of NSCLC. Median age at treatment was 75 years old; median tumor diameter was 2.48 cm, and median GTV 13.3 cc. One hundred fifty-five patients had stage IA disease (79.1%) and 41 patients stage IB disease (20.9%). Total doses ranged from 48 to 60 Gy in 3-8 fractions. Primary endpoints of the study were safety (acute and late toxicity) and efficacy (Local Control, Disease-Free Survival, Overall and Cancer-SpecificSurvival). Results: Median follow-up time was 30 months. The percentage of grade >= 2 pulmonary toxicity was 3%, and the 30 and 60 days mortality rate was 0%. Local Recurrence-Free Survival was 89.7% at 3 years. Fifty-nine patients (30.1%) had at least one failure (local and/ornodaland/ordistant),with a Disease-Free Survival (DFS) rate at 3 years of 65.5%. Overall Survival (OS) and Cancer-Specific Survival (CSS) rates were 68% and 82.1% at 3 years, respectively. Median time to any recurrence was 15 months, while median overall survival time was 54 months. At multivariate analysis, stage IB was the only variable associated to a decrease in DFS, OS and CSS (HR 2.77, p = 0.006; HR 2.38, p = 0.009; HR 4.06, p <= 0.001, respectively). A difference in survival according to stage was also evident at the log-rank test (p <= 0.0001 for CSS and OS). Conclusion: The results of the present study support the routine use of SABR for stage I NSCLC in a daily practice environment. The only prognostic factor that has been confirmed by our analysis was tumor stage (IA vs. IB). (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:248 / 253
页数:6
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