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High‐dose methotrexate following intravitreal methotrexate administration in preventing central nervous system involvement of primary intraocular lymphoma

机译:玻璃体内注射甲氨蝶呤后大剂量甲氨蝶呤可预防原发性眼内淋巴瘤的中枢神经系统受累

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摘要

In order to prevent central nervous system (CNS) involvement and improve the prognosis of primary intraocular lymphoma (PIOL), we prospectively evaluated the efficacy of combined therapy using intravitreal methotrexate (MTX) and systemic high‐dose MTX on treatment‐naïve PIOL. Patients with newly diagnosed PIOL whose lymphoma was limited to the eyes were enrolled. The patients were treated with weekly intravitreal MTX until the ocular lesions were resolved, followed by five cycles of systemic high‐dose MTX (3.5 g/m2) every other week. Ten patients were enrolled in this study and completed the treatment. All patients achieved complete response for their ocular lesions with rapid decrease of intravitreal interleukin‐10 concentration. Adverse events of intravitreal and systemic high‐dose MTX were mild and tolerable. With a median follow‐up of 29.5 months, four patients (40%) experienced the CNS disease development and the mean CNS lymphoma‐free survival (CLFS) time was 51.1 months. Two‐year CLFS, which was the primary end‐point of the study, was 58.3% (95% confidence interval, 23.0–82.1%). In contrast, eight patients were treated with intravitreal MTX alone in our institute, and their 2‐year CLFS was 37.5% (95% confidence interval, 8.7–67.4%). In conclusion, systemic high‐dose MTX following intravitreal style="fixed-case">MTX is feasible and might be effective in preventing style="fixed-case">CNS involvement of style="fixed-case">PIOL. Further arrangements are worth considering in order to improve the effects. This study was registered with style="fixed-case">UMIN Clinical Trials Registry ( style="fixed-case">UMIN000003921).
机译:为了预防中枢神经系统(CNS)受累并改善原发性眼内淋巴瘤(PIOL)的预后,我们前瞻性地评估了玻璃体内注射甲氨蝶呤(MTX)和全身高剂量MTX联合治疗未治疗过的PIOL的疗效。纳入新诊断为PIOL的淋巴瘤仅限于眼睛的患者。患者每周接受玻璃体内MTX治疗直至眼部病变得到解决,然后每两周进行五个周期的全身高剂量MTX(3.5 g / m 2 )治疗。十名患者参加了本研究并完成了治疗。所有患者的眼部病变均获得了完全缓解,玻璃体内白介素10浓度迅速降低。玻璃体内和全身高剂量MTX的不良反应轻微且可以忍受。中位随访29.5个月,四名患者(40%)经历了中枢神经系统疾病的发展,中枢神经系统无淋巴瘤生存(CLFS)的平均时间为51.1个月。两年期CLFS是研究的主要终点,为58.3%(95%置信区间为23.0-82.1%)。相比之下,在我们研究所,仅使用玻璃体内MTX治疗的八名患者,其两年CLFS为37.5%(95%置信区间为8.7–67.4%)。总之,玻璃体腔内 style =“ fixed-case”> MTX 后的全身大剂量MTX是可行的,并且可以有效地预防 style =“ fixed-case”> CNS 的介入 style =“ fixed-case”> PIOL 。为了改善效果,值得考虑进一步的安排。该研究已在 style =“ fixed-case”> UMIN 临床试验注册中心( style =“ fixed-case”> UMIN 000003921)注册。

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