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立体定向体部放疗治疗大于 5cm 的非小细胞肺癌肿瘤:安全性和有效性。

Stereotactic Body Radiation Therapy for Non-Small Cell Lung Cancer Tumors Greater Than 5 cm: Safety and Efficacy.

机构信息

Department of Radiation Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.

Department of Radiation Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.

出版信息

Int J Radiat Oncol Biol Phys. 2015 Jun 1;92(2):325-31. doi: 10.1016/j.ijrobp.2015.01.045. Epub 2015 Apr 1.

Abstract

PURPOSE

The purpose of this study was to determine outcomes of patients with node-negative medically inoperable non-small cell lung cancer (NSCLC) whose primary tumors exceeded 5 cm and were treated with stereotactic body radiation therapy (SBRT).

METHODS AND MATERIALS

We surveyed our institutional prospective lung SBRT registry to identify treated patients with tumors >5 cm. Treatment outcomes for local control (LC), locoregional control (LRC), disease-free survival (DFS), and overall survival (OS) were assessed by Kaplan-Meier estimates. Toxicities were graded according to Common Terminology Criteria for Adverse Events version 4. Mean pretreatment pulmonary function test values were compared to mean posttreatment values.

RESULTS

From December 2003 to July 2014, 40 patients met study criteria. Median follow-up was 10.8 months (range: 0.4-70.3 months). Median age was 76 years (range: 56-90 years), median body mass index was 24.3 (range: 17.7-37.2), median Karnofsky performance score was 80 (range: 60-90), and median Charlson comorbidity index score was 2 (range: 0-5). Median forced expiratory volume in 1 second (FEV1) was 1.41 L (range: 0.47-3.67 L), and median diffusion capacity (DLCO) was 47% of predicted (range: 29%-80%). All patients were staged by fluorodeoxyglucose-positron emission tomography/computed tomography staging, and 47.5% underwent mediastinal staging by endobronchial ultrasonography. Median tumor size was 5.6 cm (range: 5.1-10 cm), median SBRT dose was 50 Gy (range: 30-60 Gy) in 5 fractions (range: 3-10 fractions). Eighteen-month LC, LRC, DFS, and OS rates were 91.2%, 64.4%, 34.6%, and 59.7%, respectively. Distant failure was the predominant pattern of failure (32.5%). Three patients (7.5%) experienced grade 3 or higher toxicity. Mean posttreatment FEV1 was not significantly reduced (P=.51), but a statistically significant absolute 6.5% (P=.03) reduction in DLCO was observed.

CONCLUSIONS

Lung SBRT for medically inoperable node-negative NSCLC with primary tumors larger than 5 cm is safe and provides excellent local control with limited toxicity. The predominant pattern of failure in this population was distant failure.

摘要

目的

本研究旨在确定接受立体定向体部放疗(SBRT)治疗的无法手术的局部晚期非小细胞肺癌(NSCLC)患者的治疗结局,这些患者的肿瘤直径大于 5cm,且无淋巴结转移。

方法和材料

我们调查了我们机构前瞻性的肺部 SBRT 登记处,以确定治疗肿瘤大于 5cm 的患者。通过 Kaplan-Meier 估计评估局部控制(LC)、局部区域控制(LRC)、无疾病生存(DFS)和总生存(OS)的治疗结果。毒性根据不良事件通用术语标准 4.0 版进行分级。比较治疗前和治疗后的平均肺功能测试值。

结果

2003 年 12 月至 2014 年 7 月,共有 40 名患者符合研究标准。中位随访时间为 10.8 个月(范围:0.4-70.3 个月)。中位年龄为 76 岁(范围:56-90 岁),中位体重指数为 24.3(范围:17.7-37.2),中位 Karnofsky 表现评分 80 分(范围:60-90 分),中位 Charlson 合并症指数评分为 2 分(范围:0-5 分)。中位用力呼气量 1 秒(FEV1)为 1.41L(范围:0.47-3.67L),弥散量(DLCO)中位值为预计值的 47%(范围:29%-80%)。所有患者均通过氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描分期,47.5%的患者通过支气管内超声进行纵隔分期。中位肿瘤大小为 5.6cm(范围:5.1-10cm),中位 SBRT 剂量为 50Gy(范围:30-60Gy),分 5 次(范围:3-10 次)。18 个月时的 LC、LRC、DFS 和 OS 率分别为 91.2%、64.4%、34.6%和 59.7%。远处失败是主要的失败模式(32.5%)。3 名患者(7.5%)出现 3 级或更高的毒性。治疗后 FEV1 无显著降低(P=.51),但 DLCO 绝对值显著降低 6.5%(P=.03)。

结论

对于无法手术的局部晚期无淋巴结转移 NSCLC 患者,肿瘤直径大于 5cm 时,采用立体定向体部放疗是安全的,可提供良好的局部控制,且毒性有限。该人群的主要失败模式是远处失败。

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