Gallogly James A, Jumaily Mejd, Faraji Farhoud, Mikulec Anthony A
Saint Louis University School of Medicine, Department of Otolaryngology - Head and Neck Surgery, 3635 Vista Ave, 6FDT, St. Louis, MO 63110, USA.
Am J Otolaryngol. 2018 Sep-Oct;39(5):561-566. doi: 10.1016/j.amjoto.2018.06.017. Epub 2018 Jun 22.
This study evaluates the rates of tumor control, hearing preservation and cranial nerve toxicity with the use of CyberKnife stereotactic radiotherapy consisting of 2100 cGy to the 80% isodose line delivered in three weekly fractions to treat vestibular schwannomas.
Retrospective chart review of vestibular schwannoma patients treated with CyberKnife stereotactic radiotherapy or undergoing watchful waiting between 2006 and 2017 was performed. For inclusion, patients receiving CyberKnife stereotactic radiotherapy must have had pretreatment magnetic resonance imaging and audiography, and 2 follow-up magnetic resonance imaging and audiograms. Watchful waiting patients must have had a minimum of 2 magnetic resonance imaging and 2 audiograms.
Forty patients met inclusion criteria. Twenty-two underwent CyberKnife stereotactic radiotherapy. Eighteen remain in watchful waiting. Crude tumor control was 86.4% at mean radiographic follow-up of 52.3 months. Kaplan-Meier progression-free survival was 76.9% at 5 years. Kaplan-Meier survival from radiographic growth was 61.5% at 5 years. Kaplan-Meier hearing preservation was 17.5% at 5 years. All patients undergoing watchful waiting presenting with serviceable hearing maintained serviceable hearing. Serviceable hearing among CyberKnife stereotactic radiotherapy patients was 42.9% prior to treatment and 14.2% through mean follow-up of 53.7 months. One patient experienced trigeminal nerve toxicity 45 months after SRT. 95.5% of CyberKnife stereotactic radiotherapy patients were complication-free.
Our fractionation regimen provides tumor control consistent with current literature. Hearing outcomes, however, should be discussed with patients prior to CyberKnife stereotactic radiotherapy.
本研究评估使用射波刀立体定向放射治疗(分三周三次给予 2100 cGy 至 80%等剂量线)治疗前庭神经鞘瘤时的肿瘤控制率、听力保留率和颅神经毒性。
对 2006 年至 2017 年间接受射波刀立体定向放射治疗或进行观察等待的前庭神经鞘瘤患者进行回顾性病历审查。纳入标准为,接受射波刀立体定向放射治疗的患者必须有治疗前的磁共振成像和听力图,以及两次随访磁共振成像和听力图。观察等待的患者必须至少有两次磁共振成像和两次听力图。
40 名患者符合纳入标准。22 名接受了射波刀立体定向放射治疗。18 名仍在观察等待。在平均影像学随访 52.3 个月时,粗略肿瘤控制率为 86.4%。5 年时的 Kaplan-Meier 无进展生存率为 76.9%。5 年时影像学生长后的 Kaplan-Meier 生存率为 61.5%。5 年时的 Kaplan-Meier 听力保留率为 17.5%。所有进行观察等待且听力尚可的患者均保持了尚可的听力。射波刀立体定向放射治疗患者治疗前的尚可听力为 42.9%,在平均随访 53.7 个月时为 14.2%。1 名患者在立体定向放射治疗后 45 个月出现三叉神经毒性。95.5%的射波刀立体定向放射治疗患者无并发症。
我们的分割方案提供了与当前文献一致的肿瘤控制。然而,在进行射波刀立体定向放射治疗前,应与患者讨论听力结果。