Pennathur Arjun, Luketich James D, Heron Dwight E, Abbas Ghulam, Burton Steven, Chen Mang, Gooding William E, Ozhasoglu Cihat, Landreneau Rodney J, Christie Neil A
Heart, Lung, and Esophageal Surgery Institute, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.
J Thorac Cardiovasc Surg. 2009 Mar;137(3):597-604. doi: 10.1016/j.jtcvs.2008.06.046.
Surgical resection is the standard of care for patients with stage I non-small cell lung cancer. For high-risk patients, however, stereotactic radiosurgery may offer an alternative. We report our initial experience with stereotactic radiosurgery for treatment of stage I non-small cell lung cancer by a team of thoracic surgeons and radiation oncologists.
Patients medically ineligible for operation were offered stereotactic radiosurgery. Thoracic surgeons evaluated all patients, placed fiducials, and performed treatment planning in collaboration with radiation oncologists. Median dose of 20 Gy to 80% isodose line was administered as single fraction (range 20-60 Gy,1-3 fractions). Initial response rate, progression, and survival were monitored.
Twenty-one patients underwent stereotactic radiosurgery in 3 years. Fiducial placement resulted in pneumothorax requiring a pigtail catheter in 10 of 21 patients (47%). Disease showed initial response in 12 of 21 patients (57%), was stable in 5 (24%), progressed in 3 (14%), and was not evaluable in 1 (5%). Procedure-related mortality was zero. With mean 24-month follow-up, estimated 1-year survival probability was 81% (68% confidence interval 0.73-0.90). Median survival was 26.4 months (confidence interval 19.6 months-not reached). Local progression occurred in 9 patients (42%). Median time to local progression was 12.3 months (confidence interval 12 months-not reached).
Preliminary experience indicates that stereotactic radiosurgery (median dose 20 Gy) is safe in this high-risk group; however, it was associated with significant local progression. Further prospective studies with multiple fractions are needed to evaluate its efficacy in this population.
手术切除是Ⅰ期非小细胞肺癌患者的标准治疗方法。然而,对于高危患者,立体定向放射外科可能是一种替代方案。我们报告了一组胸外科医生和放射肿瘤学家使用立体定向放射外科治疗Ⅰ期非小细胞肺癌的初步经验。
对医学上不适合手术的患者提供立体定向放射外科治疗。胸外科医生对所有患者进行评估,放置基准标记,并与放射肿瘤学家合作进行治疗计划。对80%等剂量线给予20 Gy的中位剂量,作为单次分割剂量(范围20 - 60 Gy,1 - 3次分割)。监测初始缓解率、疾病进展和生存率。
21例患者在3年内接受了立体定向放射外科治疗。在21例患者中有10例(47%)因放置基准标记导致气胸,需要放置猪尾导管。21例患者中有12例(57%)疾病出现初始缓解,5例(24%)病情稳定,3例(14%)病情进展,1例(5%)无法评估。与手术相关的死亡率为零。平均随访24个月,估计1年生存率为81%(68%置信区间0.73 - 0.90)。中位生存期为26.4个月(置信区间19.6个月 - 未达到)。9例患者(42%)出现局部进展。局部进展的中位时间为12.3个月(置信区间12个月 - 未达到)。
初步经验表明,立体定向放射外科(中位剂量20 Gy)在这一高危组中是安全的;然而,它与显著的局部进展相关。需要进一步进行多分割的前瞻性研究来评估其在该人群中的疗效。