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Clinical outcomes of image-guided proton therapy for histologically confirmed stage I non-small cell lung cancer

机译:影像学指导的质子治疗在组织学上证实的I期非小细胞肺癌的临床结果

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Two prospective phase II trials were designed to assess the efficacy and safety of image-guided proton therapy (IGPT) for either medically inoperable or operable stage I non-small cell lung cancer (NSCLC). The present study reports the interim results of these trials. Fifty-five patients with histologically confirmed stage I NSCLC (IA in 33 patients and IB in 22 patients; inoperable in 21 patients and operable in 34 patients) who received IGPT between July 2013 and February 2017 were analyzed. The median patient age was 71?years (range: 48–88?years). IGPT with fiducial metallic marker matching was performed for suitable patients, and a respiratory gating method for motion management was used for all treatments. Peripherally located tumors were treated with 66?Gy relative biological effectiveness equivalents (Gy(RBE)) in 10 fractions (n?=?49) and centrally located tumors were treated with 72.6?Gy(RBE) in 22 fractions (n?=?6). Treatment associated toxicities were evaluated using Common Toxicity Criteria for Adverse Events (v.4.0). Median follow-up was 35?months (range: 12–54?months) for survivors. For all patients, the 3-year overall survival, progression-free survival, and local control rates were 87% (95% confidence interval: 73–94%), 74% (58–85%), and 96% (83–99%), respectively. Fiducial marker matching was used in 39 patients (71%). Grade 2 toxicities observed were radiation pneumonitis in 5 patients (9%), rib fracture in 2 (4%), and chest wall pain in 5 (9%). There were no grade 3 or higher acute or late toxicities. IGPT appears to be effective and well tolerated for all patients with stage I NSCLC. Lung-001, 13–02-09 (9), registered 11 June 2013 and Lung-002, 13–02-10 (10), registered 11 June 2013.
机译:设计了两项前瞻性II期临床试验,以评估图像指导质子治疗(IGPT)对于不可手术或不可手术的I期非小细胞肺癌(NSCLC)的疗效和安全性。本研究报告了这些试验的中期结果。分析了在2013年7月至2017年2月间接受IGPT的55例经组织学证实为I期NSCLC的患者(IA占33例,IB占22例; 21例不能手术,34例可手术)。患者中位年龄为71岁(范围:48-88岁)。对合适的患者进行了具有基准金属标记匹配的IGPT,并采用了用于运动控制的呼吸门控方法进行所有治疗。位于周围的肿瘤用10个组分中的66?Gy相对生物学等效量(Gy(RBE))(n?=?49)进行治疗,位于中心的肿瘤则以22个组分中的72.6?Gy(RBE)进行治疗(n?=?49)。 6)。使用与不良事件有关的通用毒性标准(v.4.0)评估与治疗相关的毒性。幸存者的中位随访时间为35个月(范围:12-54个月)。对于所有患者,3年总生存率,无进展生存率和局部控制率分别为87%(95%置信区间:73-94%),74%(58-85%)和96%(83- 99%)。 39例患者(71%)使用了基准标记匹配。观察到的2级毒性是放射性肺炎5例(9%),肋骨骨折2例(4%)和胸壁痛5例(9%)。没有3级或更高的急性或晚期毒性。对于所有I期NSCLC患者,IGPT似乎有效且耐受性良好。 2013年6月11日注册的Lung-001,13-02-09(9),2013年6月11日注册的Lung-002,13-02-02(10)。

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