Hamilton Sarah Nicole, Nichol Alan, Truong Pauline, McKenzie Michael, Hsu Fred, Cheung Arthur, Dolman Peter, Gete Ermias, Ma Roy
British Columbia Cancer Agency (BCCA).
University of British Columbia, Vancouver, British Columbia, Canada.
Ophthalmic Plast Reconstr Surg. 2018 May/Jun;34(3):217-221. doi: 10.1097/IOP.0000000000000914.
To review the outcomes of patients with optic nerve sheath meningiomas (ONSM) treated with fractionated stereotactic radiotherapy.
Patient characteristics, treatment, and outcomes were analyzed for all patients with primary and secondary ONSM treated from 2001 to 2012. Clinically significant visual acuity change was defined as a 2-line change on the Snellen eye chart from pre-fractionated stereotactic radiotherapy.
Forty-one patients were treated: 23 patients with primary ONSM and 18 patients with secondary ONSM. The median age at diagnosis was 56 years. The median visual follow up was 3.8 years and the median radiologic follow up was 4.4 years. At diagnosis, 36% had normal vision (20/20-20/40), 10% had mild impairment (<20/40-20/60), 20% had moderate visual impairment (<20/60-20/200), 27% had severe impairment (<20/200), and 7% had no light perception. Common acute side effects were headache (32%) and nausea (15%); 15% of patients required corticosteroids during stereotactic radiotherapy. Chronic toxicities included retinopathy (7%), pituitary dysfunction (13%), chronic ocular pain (5%), and cataracts (2%). Visual acuity was stable in 65%, improved in 27%, and decreased in 8% of patients. Visual fields were stable in 70%, improved in 21%, and reduced in 9%. Actuarial 5-year local control rates were 100% for primary ONSM and 88% for secondary ONSM. Actuarial 5-year visual preservation rates were 100% for primary ONSM and 86% for secondary ONSM.
Fractionated stereotactic radiotherapy for primary and secondary ONSM was well tolerated and provides excellent local control and visual preservation. Longer follow up is required to determine the risk of late ocular and pituitary sequelae.
回顾接受分次立体定向放射治疗的视神经鞘膜瘤(ONSM)患者的治疗结果。
分析了2001年至2012年期间接受治疗的所有原发性和继发性ONSM患者的特征、治疗方法及结果。临床显著视力变化定义为与分次立体定向放射治疗前相比,Snellen视力表上视力下降2行。
共治疗41例患者,其中23例原发性ONSM患者,18例继发性ONSM患者。诊断时的中位年龄为56岁。视力随访的中位时间为3.8年,影像学随访的中位时间为4.4年。诊断时,36%视力正常(20/20 - 20/40),10%有轻度损害(<20/40 - 20/60),20%有中度视力损害(<20/60 - 20/200),27%有重度损害(<20/200),7%无光感。常见的急性副作用为头痛(32%)和恶心(15%);15%的患者在立体定向放射治疗期间需要使用皮质类固醇。慢性毒性包括视网膜病变(7%)、垂体功能障碍(13%)、慢性眼痛(5%)和白内障(2%)。65%的患者视力稳定,27%的患者视力改善,8%的患者视力下降;70%的患者视野稳定,21%改善,9%缩小。原发性ONSM的5年精算局部控制率为100%,继发性ONSM为88%。原发性ONSM的5年精算视力保留率为100%,继发性ONSM为86%。
原发性和继发性ONSM的分次立体定向放射治疗耐受性良好,能提供出色的局部控制和视力保留效果。需要更长时间的随访以确定眼部和垂体晚期后遗症的风险。