Department of Radiation Oncology, Stanford University School of Medicine, Stanford, California.
Division of Cardiovascular Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Pract Radiat Oncol. 2017 Nov-Dec;7(6):e525-e529. doi: 10.1016/j.prro.2017.04.005. Epub 2017 Apr 13.
Stereotactic ablative radiation therapy (SABR) is an established treatment for selected lung tumors. Sinoatrial node (SAN) toxicity after thoracic SABR has not been reported in the literature. We sought to understand the risk of SAN toxicity owing to incidental dose to the SAN from SABR.
We conducted a retrospective review of patients with early-stage lung cancer or limited pulmonary metastases who underwent thoracic SABR to a right-sided central lung tumor (within 2 cm of the mainstem bronchus or other mediastinal structures) between January 2008 and December 2014, analyzed a subset whose treatment imparted dose to the SAN exceeding 10% of the prescription dose, and examined patient and treatment dosimetric characteristics. Mean follow-up interval was 28 months. Time to toxicity was defined from start of SABR.
Of 47 patients with central tumors in the right lung treated with SABR reviewed, 13 met our study criteria. A contouring atlas of regional cardiac anatomy was created. One patient treated with SABR for non-small cell lung cancer at the right hilum developed symptomatic sick sinus syndrome, requiring pacemaker placement 6 months after treatment. Her acute presentation and short interval between SABR and onset of symptoms suggest that SAN toxicity was likely due to radiation-induced injury. Both her age and mean dose to her SAN were the third highest in our cohort. She remained free from cancer progression at 24 months' follow-up. Twelve additional patients who received significant dose to the SAN from SABR did not develop toxicity.
While uncommon, SAN toxicity from SABR to right-sided central thoracic tumors should be recognized and followed in future studies.
立体定向消融放疗(SABR)是一种治疗选定的肺部肿瘤的既定方法。在文献中尚未报道过胸部 SABR 后窦房结(SAN)毒性。我们试图了解由于 SABR 对 SAN 的偶然剂量而导致 SAN 毒性的风险。
我们对 2008 年 1 月至 2014 年 12 月期间接受右侧中央肺部肿瘤(主支气管或其他纵隔结构 2 厘米内)的胸部 SABR 的早期肺癌或局限性肺转移患者进行了回顾性研究,分析了部分患者的治疗方案,这些方案对 SAN 施加的剂量超过处方剂量的 10%,并检查了患者和治疗剂量学特征。平均随访时间为 28 个月。毒性发生时间定义为 SABR 开始后的时间。
在接受 SABR 治疗的 47 例右侧中央肿瘤患者中,有 13 例符合我们的研究标准。创建了区域心脏解剖轮廓图。1 例在右肺门接受 SABR 治疗非小细胞肺癌的患者出现症状性窦性心动过缓综合征,在治疗后 6 个月需要植入起搏器。她的急性表现和 SABR 与症状发作之间的短暂间隔表明,SAN 毒性可能是由于辐射引起的损伤。她的年龄和 SAN 的平均剂量均为我们队列中的第三高。在 24 个月的随访中,她仍然没有癌症进展。另外 12 名从 SABR 中接受大量 SAN 剂量的患者没有发生毒性。
虽然不常见,但应认识到并在未来的研究中跟踪 SABR 治疗右侧中央胸部肿瘤引起的 SAN 毒性。