Associated Retina Consultants Ltd, Phoenix, AZ, USA.
Clin Lymphoma Myeloma Leuk. 2012 Dec;12(6):412-7. doi: 10.1016/j.clml.2012.07.006. Epub 2012 Sep 18.
In this retrospective study on vitreoretinal lymphoma, there was significant change in diagnosis and treatment trends over 17 years at a single institution. Fine needle aspiration biopsy had replaced vitrectomy to collect vitreous sample and external beam radiotherapy in combination with systemic chemotherapy was replaced by intravitreal methotrexate and rituximab, which regressed vitreoretinal lymphoma (VRL) with no relapses or major ocular complications.
The purpose of this study was to report the changing trends in treatment (external beam radiotherapy [EBRT] and intravitreal chemotherapy) of VRL and treatment outcomes at a single institution.
A retrospective chart review of vitreous biopsy proven patients was performed. The data analysis included demographics, systemic lymphoma status, ocular symptoms, clinical and immunocytological findings, treatment methods, and response (intravitreal methotrexate 300 μg/0.05 mL, 1000 μg/0.1 mL of rituximab and EBRT 36-45 Gy) and ocular and systemic lymphoma outcomes at last follow-up.
Twelve eyes of 8 patients had intraocular B-cell lymphoma (median age, 61 years; range, 50-83). Central nervous system non-Hodgkin's lymphoma (CNS-NHL) was present in 7 of 8 patients. Most common ocular symptoms were diminution of vision in 4 and floaters in 3 patients. Iritis and uveitis were found in 6 eyes and vitritis in 11 eyes. Retinal infiltrates were present in 8 eyes. Immunocytology revealed elevated levels of interleukin (IL)-10 (12,783.5 pg/mL), IL-6 (26.7 pg/mL), and IgH gene rearrangement. Three patients were treated with EBRT, 6 eyes with intravitreal methotrexate (median, 9.5; range, 2-15), and 2 eyes with intravitreal rituximab injections (median, 4; range, 2-6). Two patients developed marked keratitis because of methotrexate toxicity. At median follow-up of 33.5 months (range, 4-96), VRL had resolved in 7 eyes and persistent in 5 eyes. One patient died because of advanced CNS-NHL.
Intravitreal chemotherapy provided good control rates for VRL patients in our limited series. Patients with associated CNS-NHL had poorer outcomes.
本研究旨在报告单中心治疗(外部束放射治疗[EBRT]和眼内化疗)脉络膜视网膜淋巴瘤(VRL)的变化趋势和治疗结果。
对玻璃体活检确诊的患者进行回顾性图表分析。数据分析包括人口统计学、全身淋巴瘤状况、眼部症状、临床和免疫细胞化学发现、治疗方法以及反应(眼内甲氨蝶呤 300μg/0.05mL,利妥昔单抗 1000μg/0.1mL 和 EBRT 36-45Gy)以及最后随访时的眼部和全身淋巴瘤结局。
8 例患者的 12 只眼患有眼内 B 细胞淋巴瘤(中位年龄 61 岁;范围 50-83 岁)。7 例患者存在中枢神经系统非霍奇金淋巴瘤(CNS-NHL)。最常见的眼部症状是 4 例视力下降和 3 例飞蚊症。6 只眼有虹膜炎和葡萄膜炎,11 只眼有玻璃体炎。8 只眼有视网膜浸润。免疫细胞化学显示白细胞介素(IL)-10(12783.5pg/mL)、IL-6(26.7pg/mL)和 IgH 基因重排水平升高。3 例患者接受 EBRT,6 只眼接受眼内甲氨蝶呤治疗(中位数 9.5;范围 2-15),2 只眼接受眼内利妥昔单抗注射(中位数 4;范围 2-6)。2 例患者因甲氨蝶呤毒性出现明显角膜炎。中位随访 33.5 个月(范围 4-96)后,7 只眼 VRL 缓解,5 只眼持续存在。1 例患者因晚期 CNS-NHL 死亡。
在我们的有限系列中,眼内化疗为 VRL 患者提供了良好的控制率。伴发 CNS-NHL 的患者结局较差。