Department of Radiation Oncology, IRCCS Istituto Clinico Humanitas, Milano (Rozzano), Italy.
Radiat Oncol. 2010 Oct 15;5:94. doi: 10.1186/1748-717X-5-94.
To report acute toxicity, initial outcome results and planning therapeutic parameters in radiation treatment of advanced lung cancer (stage III) with volumetric modulated arcs using RapidArc (RA).
Twenty-four consecutive patients were treated with RA. All showed locally advanced non-small cell lung cancer with stage IIIA-IIIB and with large volumes (GTV:299 ± 175 cm3, PTV:818 ± 206 cm3). Dose prescription was 66Gy in 33 fractions to mean PTV. Delivery was performed with two partial arcs with a 6 MV photon beam.
From a dosimetric point of view, RA allowed us to respect most planning objectives on target volumes and organs at risk. In particular: for GTV D1% = 105.6 ± 1.7%, D99% = 96.7 ± 1.8%, D5%-D95% = 6.3 ± 1.4%; contra-lateral lung mean dose resulted in 13.7 ± 3.9Gy, for spinal cord D1% = 39.5 ± 4.0Gy, for heart V45Gy = 9.0 ± 7.0Gy, for esophagus D1% = 67.4 ± 2.2Gy. Delivery time was 133 ± 7s. At three months partial remission > 50% was observed in 56% of patients. Acute toxicities at 3 months showed 91% with grade 1 and 9% with grade 2 esophageal toxicity; 18% presented grade 1 and 9% with grade 2 pneumonia; no grade 3 acute toxicity was observed. The short follow-up does not allow assessment of local control and progression free survival.
RA proved to be a safe and advantageous treatment modality for NSCLC with large volumes. Long term observation of patients is needed to assess outcome and late toxicity.
报告使用容积旋转调强技术(RapidArc,RA)治疗晚期肺癌(III 期)的急性毒性、初步结果和治疗参数计划。
24 例连续患者接受 RA 治疗。所有患者均为局部晚期非小细胞肺癌,III 期 A 期至 IIIB 期,且肿瘤体积较大(GTV:299 ± 175 cm3,PTV:818 ± 206 cm3)。剂量处方为 66Gy,分 33 次给予平均 PTV。使用 6 MV 光子束进行两次部分弧治疗。
从剂量学角度来看,RA 使我们能够在靶区和危及器官上满足大多数计划目标。特别是:GTV D1% = 105.6 ± 1.7%,D99% = 96.7 ± 1.8%,D5%-D95% = 6.3 ± 1.4%;对侧肺平均剂量为 13.7 ± 3.9Gy,脊髓 D1% = 39.5 ± 4.0Gy,心脏 V45Gy = 9.0 ± 7.0Gy,食管 D1% = 67.4 ± 2.2Gy。治疗时间为 133 ± 7s。3 个月时,56%的患者观察到部分缓解>50%。3 个月时的急性毒性反应显示,91%的患者为 1 级,9%的患者为 2 级食管毒性;18%的患者出现 1 级,9%的患者出现 2 级肺炎;未观察到 3 级急性毒性。短期随访不能评估局部控制和无进展生存期。
RA 被证明是治疗大体积非小细胞肺癌的一种安全且有利的治疗方式。需要对患者进行长期观察,以评估结果和迟发性毒性。