Lanciano R, Fowble B, Sergott R C, Atlas S, Savino P J, Bosley T M, Rubenstein J
Department of Radiation Oncology, Hospital of the University of Pennsylvania, Philadelphia.
Int J Radiat Oncol Biol Phys. 1990 Feb;18(2):407-11. doi: 10.1016/0360-3016(90)90108-v.
Between January 1982 and March 1987, 23 patients (26 orbits) were treated for orbital pseudotumor with radiation therapy at the Department of Radiation Oncology, Hospital of the University of Pennsylvania. The patients were referred for clinical relapse after steroid taper in 70%, no response to steroids in 17%, and no steroid treatment (refused or contraindicated) in 13%. Presenting symptoms/signs included soft tissue swelling in 92% of orbits, pain in 92%, proptosis in 85%, and extraocular muscle dysfunction or ptosis in 69%. Decreased visual acuity was seen in only 19% of orbits. Biopsy was performed in nine patients. Treatment consisted of 2000 cGy in 2 weeks in 10 fractions for all patients. Median follow-up was 41 months, with a mean of 53 months, and a range of 21-92 months. Complete response was documented in 87% of orbits with soft tissue swelling, 82% with proptosis, 78% with extraocular muscle dysfunction, and 75% with pain. Of the five patients with visual acuity defects, three experienced complete recovery. There was no difference in complete response in patients biopsied versus those not biopsied. Overall, 17 orbits have remained in complete orbital response with no further steroid requirement (66%). Three orbits suffered local relapse at some point following radiation therapy and were retreated with steroids. These three orbits had durable local control off steroids at last follow-up (11%). Therefore, 77% of orbits attained durable local control and were steroid independent with radiation therapy alone or radiation therapy followed by steroids for relapse. Only one patient developed systemic lymphoma with follow-up. No pretreatment clinical factor reached statistical significance with respect to prognosis following radiation therapy at the less than or equal to .05 level. There were no significant acute or chronic side effects secondary to treatment. Steroids should continue to be first line treatment for orbital pseudotumor, but radiation therapy has a well-defined role in cases of steroid failure or in patients unable to tolerate steroid therapy.
1982年1月至1987年3月期间,宾夕法尼亚大学医院放射肿瘤学系对23例(26个眼眶)眼眶假瘤患者进行了放射治疗。70%的患者因类固醇减量后临床复发前来就诊,17%的患者对类固醇无反应,13%的患者未接受类固醇治疗(拒绝或有禁忌)。主要症状/体征包括92%的眼眶出现软组织肿胀、92%的眼眶疼痛、85%的眼眶眼球突出以及69%的眼眶眼外肌功能障碍或上睑下垂。仅19%的眼眶出现视力下降。9例患者进行了活检。所有患者均接受了2周内分10次给予2000 cGy的治疗。中位随访时间为41个月,平均为53个月,范围为21 - 92个月。记录显示,软组织肿胀的眼眶中87%完全缓解,眼球突出的眼眶中82%完全缓解,眼外肌功能障碍的眼眶中78%完全缓解,疼痛的眼眶中75%完全缓解。在5例有视力缺陷的患者中,3例完全恢复。活检患者与未活检患者的完全缓解情况无差异。总体而言,17个眼眶保持完全眼眶缓解,无需进一步使用类固醇(66%)。3个眼眶在放射治疗后的某个时间点出现局部复发,并接受了类固醇再次治疗。在最后一次随访时,这3个眼眶在停用类固醇后实现了持久的局部控制(11%)。因此,77%的眼眶通过单纯放射治疗或放射治疗后复发时加用类固醇实现了持久的局部控制且无需依赖类固醇。随访中仅1例患者发生系统性淋巴瘤。在小于或等于0.05的水平上,没有预处理临床因素在放射治疗后的预后方面达到统计学意义。治疗未产生明显的急性或慢性副作用。类固醇应继续作为眼眶假瘤的一线治疗方法,但放射治疗在类固醇治疗失败或患者无法耐受类固醇治疗的情况下具有明确的作用。