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首页> 外文期刊>Cancer radiotherapie: journal de la Soci閠?fran鏰ise de radiotherapie oncologique >Feasibility and efficacy of cyberknife radiotherapy for lung cancer: Early results
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Feasibility and efficacy of cyberknife radiotherapy for lung cancer: Early results

机译:射波刀放射治疗肺癌的可行性和有效性:早期结果

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Purpose. - High-dose robotic stereotactic irradiation can be achieved with high precision using the CyberknifeM system equipped with the Synchrony respiratory tracking device. Cyberknife irradiation can overcome some limitations of conventional radiotherapy including errors due to breathing motion and patient setup. High dose levels are of interest for tumours that have shown a dose-response relationship including lung tumours. We reviewed the treatments and outcomes for the first French patients with lung tumours treated at the Cyberknife centre of Nice.Patients and methods. - Thirty four patients were treated between November 2006 and November 2007 at the Cyberknife centre of Nice, Centre Lacassagne, France. Thirty had untreated primary lung cancer, 4 had colorectal metastasis to the lung. We evaluated the feasibility and reliability of fiducial placement, toxicity and early outcomes. Objective tumour response was assessed on thoracic CT scan every three months.Results. - There was no grade 1- toxicity. Toxicity (11%) mainly consisted of grade 1-2 asthenia. Crude overall tumour response rate was 96% for all assessable patients and 91% at 3 and 6 months, respectively. The use of one fiducial ensured minimal toxicity (no grade III pneumothorax) while allowing reliable tumour tracking as shown by the low infield failure rate (no geographic miss). Diagnostic procedure was performed during fiducial placement when required.
机译:目的。 -使用配备有同步呼吸跟踪设备的Cyber​​knifeM系统,可以高精度实现大剂量机器人立体定向照射。射波刀辐照可以克服传统放疗的一些局限性,包括由于呼吸运动和患者设置引起的错误。对于显示出包括肺肿瘤在内的剂量反应关系的肿瘤,高剂量水平是令人关注的。我们回顾了在尼斯的射波刀中心治疗的首批法国肺部肿瘤患者的治疗方法和结果。 -在2006年11月至2007年11月之间,法国拉卡萨涅中心尼斯的射波刀中心对34例患者进行了治疗。 30例未经治疗的原发性肺癌,4例发生了结直肠肺转移。我们评估了基准放置,毒性和早期结果的可行性和可靠性。每三个月通过胸部CT扫描评估客观肿瘤反应。 -没有1级毒性。毒性(11%)主要包括1-2级乏力。所有可评估患者的粗略总体肿瘤缓解率分别为96%和3个月和6个月时为91%。使用一种基准可确保最低的毒性(无III级气胸),同时可进行可靠的肿瘤追踪,如低内镜失败率(无地理遗漏)所示。必要时在基准放置期间执行诊断程序。

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