CyberKnife Center of Miami, Miami, Florida, USA.
Clin Oncol (R Coll Radiol). 2009 Oct;21(8):623-31. doi: 10.1016/j.clon.2009.06.006. Epub 2009 Aug 13.
To determine the effectiveness of robotic stereotactic radiotherapy with image guidance and real-time respiratory tracking against early stage peripheral lung cancer.
We treated patients with stage I non-small cell lung cancer (NSCLC) with CyberKnife and analysed their clinical characteristics and outcomes. All patients had co-morbid conditions that precluded lobectomy. The clinical target volume (CTV) included the gross tumour volume (GTV) and a 6mm margin in all directions to account for microscopic extension. The planning target volume (PTV) equalled CTV+2mm in all directions for uncertainty. Tumour motion was tracked using a combination of Synchrony and Xsight Spine tracking methods with the aid of a single gold marker implanted in the centre of the tumour, or using the newer Xsight Lung method without markers for selected tumours. A 60-67.5 Gy dose was prescribed to the 60-80% isodose line (median 65%) and given in three to five fractions. Patients were followed every 3 months for a median of 27.5 months (range 24-53 months).
Of the 67 patients with NSCLC stage IA or IB treated between January 2004 and December 2008, we report the results of a cohort of 31 with peripheral stage I tumours of 0.6-71 cm(3) volume treated between January 2004 and December 2007 with total doses between 60 and 67.5 Gy in three to five fractions. The median D(max) was 88.2 Gy and the median V(95) of the PTV was 99.6% or 27.9 cm(3). No grade 3 or above toxicity was encountered. Four cases of radiation pneumonitis and one case of oesophagitis were observed. In those patients whose pre- and post-treatment results were available, no change in pulmonary function tests was observed. Actuarial local control was 93.2% for 1 year and 85.8% for up to 4.5 years. One-year overall survival was 93.6% and 83.5% for up to 4.5 years, as projected by Kaplan-Meier analyses.
In this small cohort of patients with stage I peripheral NSCLC, robotic stereotactic radiotherapy seems to be a safe and obviously superior alternative to conventionally fractionated radiotherapy, with results that may be approaching those obtained with lobectomy without the associated morbidity.
确定带图像引导和实时呼吸跟踪的机器人立体定向放射治疗早期周围型肺癌的疗效。
我们用 CyberKnife 治疗 I 期非小细胞肺癌(NSCLC)患者,并分析其临床特征和结果。所有患者均有合并症,不能行肺叶切除术。临床靶区(CTV)包括大体肿瘤靶区(GTV)和各方向 6mm 的边界以考虑显微镜下的扩展。计划靶区(PTV)等于CTV 各方向加 2mm 以考虑不确定性。使用单个植入肿瘤中心的金标记物或使用 Xsight Lung 方法(用于选定肿瘤)结合 Synchrony 和 Xsight Spine 跟踪方法来跟踪肿瘤运动。60-67.5Gy 剂量被规定用于 60-80%等剂量线(中位数 65%),并分 3-5 次给予。中位随访时间为 27.5 个月(范围 24-53 个月),每 3 个月随访一次。
2004 年 1 月至 2008 年 12 月期间,我们对 67 例 I 期或 IIA 期 NSCLC 患者进行了治疗,在此报告 2004 年 1 月至 2007 年 12 月期间对 31 例外周 I 期肿瘤(体积 0.6-71cm3)患者的结果,总剂量为 60-67.5Gy,分 3-5 次给予。中位 D(max)为 88.2Gy,PTV 的中位 V(95)为 99.6%或 27.9cm3。未发生 3 级或以上毒性。观察到 4 例放射性肺炎和 1 例食管炎。在那些有治疗前后结果的患者中,未观察到肺功能测试的变化。根据 Kaplan-Meier 分析,1 年和 4.5 年的局部控制率分别为 93.2%和 85.8%。1 年总生存率为 93.6%,4.5 年总生存率为 83.5%。
在这组 I 期外周型 NSCLC 患者中,机器人立体定向放疗似乎是一种安全的替代方法,明显优于常规分割放疗,结果可能接近无相关发病率的肺叶切除术。