UNASSIGNED: We performed a retrospective review of records of 116 patients diagnosed with TN who underwent frameless IGRS using a linear accelerator (LINAC) over 10 years (March 2012-February 2023). All patients had failed medical management for TN. Facial pain was graded using the Barrow Neurological Institute (BNI) scoring system. Each patient received a BNI score before frameless IGRS and following treatment. Failure was defined as a BNI score IV-V at the last follow-up and/or undergoing a salvage procedure following IGRS.
UNASSIGNED: All patients had a BNI score of either IV or V before the frameless IGRS. The mean follow-up duration for all 116 patients following IGRS was 44.1 months. Most patients (81 [69.8%]) had not undergone surgery (microvascular decompression [MVD] or rhizotomy) or stereotactic radiosurgery (SRS) for TN before frameless IGRS. A total of 41 (35.3%) patients underwent a salvage procedure (MVD, rhizotomy, or an additional IGRS) following frameless IGRS. The mean duration between the initial frameless IGRS and salvage procedure was 20.1 months. At the last follow-up, a total of 110 (94.8%) patients had a BNI score of I-III. No complications were reported after the frameless IGRS. The BNI score at the last follow-up was lower compared to the initial BNI for patients regardless of prior intervention (P < 0.001). Patients who failed IGRS had a higher BNI score at the last follow-up compared to those who did not fail IGRS (2.8 vs. 2.5, P = 0.05). Patients with pain relief had a shorter follow-up compared to those with pain refractory to SRS (38.0 vs. 55.1, P = 0.005).
UNASSIGNED: In this large cohort of patients with medically refractory TN, frameless IGRS resulted in durable pain control in the majority of patients without any toxicity.
■我们对116例诊断为TN的患者的记录进行了回顾性审查,这些患者使用线性加速器(LINAC)进行了10年(2012年3月至2023年2月)的无框IGRS。所有患者的TN医疗管理失败。使用巴罗神经研究所(BNI)评分系统对面部疼痛进行评分。每位患者在无框IGRS之前和治疗后接受BNI评分。失败定义为在最后一次随访和/或在IGRS后接受抢救程序时的BNI评分IV-V。
■所有患者在无框IGRS之前的BNI评分为IV或V。所有116例IGRS患者的平均随访时间为44.1个月。大多数患者(81[69.8%])在无框IGRS之前没有接受过TN手术(微血管减压术[MVD]或根际切开术)或立体定向放射外科(SRS)。共有41例(35.3%)患者接受了抢救程序(MVD,根际切断术,或额外的IGRS)跟随无框IGRS。初始无框IGRS和救助程序之间的平均持续时间为20.1个月。在最后一次随访中,共有110例(94.8%)患者的BNI评分为I-III.无框IGRS术后无并发症报告。与患者的初始BNI相比,末次随访时的BNI评分较低(P<0.001)。与IGRS未失败的患者相比,IGRS失败的患者在最后一次随访中的BNI评分更高(2.8vs.2.5,P=0.05)。与疼痛难治的SRS患者相比,疼痛缓解患者的随访时间较短(38.0vs.55.1,P=0.005)。
■在这个庞大的医学难治性TN患者队列中,无框IGRS可在大多数患者中实现持久的疼痛控制,无任何毒性.