Anthony Casey L, Bavinger J Clay, Shantha Jessica G, O'Keefe Ghazala D, Pearce William A, Voloschin Alfredo, Grossniklaus Hans E, Yeh Steven
Department of Ophthalmology, Emory University School of Medicine, Atlanta, GA, USA.
Department of Medicine, Hematology and Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Int J Retina Vitreous. 2021 Dec 4;7(1):72. doi: 10.1186/s40942-021-00346-0.
To describe the visual acuity and anatomic outcomes of intravitreal methotrexate (MTX) for the treatment of primary vitreoretinal lymphoma (PVRL).
Single-center retrospective case series of patients with a diagnosis of PVRL treated with intravitreal MTX. Patient records were reviewed for demographic information, ocular exam findings, and treatment regimens including number of MTX injections. Clinical outcomes recorded included visual acuity (VA), time to partial (PR) or complete response (CR), disease-free survival, time to relapse, and any CNS progression.
Ten eyes of 7 patients (4 male, 6 female) were reviewed. The mean age ± standard deviation (SD) was 70 ± 12 years. Five patients had prior or concomitant diagnosis of primary CNS lymphoma with a history of systemic chemotherapy including MTX. Three eyes (30%) exhibited isolated vitreous involvement, four (40%) had subretinal lesions, and three (30%) presented with both vitreous and subretinal disease. Mean initial logMAR VA was 0.38 ± 0.52 (Snellen visual equivalent 20/50), while mean final logMAR VA ± SD was 0.34 ± 0.27 (Snellen visual equivalent 20/40) with a mean follow-up time of 26 months (Range, 3-49 months). Patients received an average of 6 intravitreal MTX injections (Range 1-10) over the course of treatment. Two patients received concomitant systemic chemotherapy. Mean time to either PR or CR was 57 days, and 6 eyes (60%) exhibited regression with no relapse after local treatment. For the 4 eyes that eventually relapsed, the mean time ± SD to first relapse was 193 days ± 155 days, and one eye experienced a second relapse. Two of 3 patients with subretinal disease showed complete regression with extended follow-up of 1 and 4 years following treatment with less than 3 doses of intravitreal MTX. One patient with PVRL developed CNS lymphoma during the study period. VA remained stable overall between the initial treatment visit, 3, 6, and 12-months (P > 0.05 for paired comparisons of VA over time).
Intravitreal methotrexate was well-tolerated and led to local disease response in the majority of patients at approximately 2 months after initiation of treatment of intraocular lymphoma. Further studies on the efficacy of intravitreal treatment alone versus combined systemic and intravitreal treatment are warranted.
描述玻璃体内注射甲氨蝶呤(MTX)治疗原发性玻璃体视网膜淋巴瘤(PVRL)的视力和解剖学结果。
对诊断为PVRL并接受玻璃体内MTX治疗的患者进行单中心回顾性病例系列研究。查阅患者记录以获取人口统计学信息、眼部检查结果以及治疗方案,包括MTX注射次数。记录的临床结果包括视力(VA)、部分缓解(PR)或完全缓解(CR)时间、无病生存期、复发时间以及任何中枢神经系统进展情况。
对7例患者(4例男性,6例女性)的10只眼进行了回顾。平均年龄±标准差(SD)为70±12岁。5例患者先前或同时诊断为原发性中枢神经系统淋巴瘤,有全身化疗史,包括使用MTX。3只眼(30%)表现为孤立性玻璃体受累,4只眼(40%)有视网膜下病变,3只眼(30%)同时有玻璃体和视网膜下病变。初始平均对数最小分辨角视力(logMAR VA)为0.38±0.52(Snellen视力等效值20/50),而最终平均logMAR VA±SD为0.34±0.27(Snellen视力等效值20/40),平均随访时间为26个月(范围3 - 49个月)。患者在治疗过程中平均接受了6次玻璃体内MTX注射(范围1 - 10次)。2例患者接受了全身化疗。达到PR或CR的平均时间为57天,6只眼(60%)在局部治疗后病情缓解且无复发。对于最终复发的4只眼,首次复发的平均时间±SD为193天±155天,1只眼经历了第二次复发。3例有视网膜下病变的患者中,2例在接受少于3次玻璃体内MTX治疗后,经过1年和4年的延长随访显示完全缓解。1例PVRL患者在研究期间发生了中枢神经系统淋巴瘤。在初始治疗就诊、3个月、6个月和12个月时,VA总体保持稳定(随时间进行VA配对比较,P>0.05)。
玻璃体内注射甲氨蝶呤耐受性良好,在眼内淋巴瘤治疗开始后约2个月时,大多数患者出现局部疾病缓解。有必要进一步研究单独玻璃体内治疗与全身和玻璃体内联合治疗的疗效。