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玻璃体腔注射甲氨蝶呤联合免疫化疗,随后进行低剂量全脑放疗用于新诊断的B细胞原发性眼内淋巴瘤。

Combined intravitreal methotrexate and immunochemotherapy followed by reduced-dose whole-brain radiotherapy for newly diagnosed B-cell primary intraocular lymphoma.

作者信息

Kaburaki Toshikatu, Taoka Kazuki, Matsuda Junko, Yamashita Hideomi, Matsuda Izuru, Tsuji Hideki, Tanaka Rie, Nakazaki Kumi, Nakamura Fumihiko, Kamiya Kohei, Kurokawa Mineo, Ohtomo Kuni, Aihara Makoto

机构信息

Department of Ophthalmology, The University of Tokyo Hospital, Tokyo, Japan.

Department of Haematology and Oncology, The University of Tokyo Hospital, Tokyo, Japan.

出版信息

Br J Haematol. 2017 Oct;179(2):246-255. doi: 10.1111/bjh.14848. Epub 2017 Jul 12.

DOI:10.1111/bjh.14848
PMID:28699673
Abstract

Primary intraocular lymphoma (IOL) has a propensity for central nervous system (CNS) relapse within 2 years of initial diagnosis, affecting clinical outcome. To reduce CNS relapse, we performed the combination treatment protocols of intravitreal methotrexate injections, methotrexate-based systemic induction chemotherapy and consolidation high-dose cytarabine and reduced-dose whole brain radiation therapy (rdWBRT, 23·4 Gy) for B-cell primary IOL with or without newly diagnosed CNS involvement. All patients underwent longitudinal brain magnetic resonance imaging (MRI) and cognitive assessment for evaluation of treatment-induced leucoencephalopathy. Seventeen patients initiated and 16 completed the protocol treatment. CNS relapse occurred in 2 patients and intraocular relapse in 3. Four-year progression-free survival (PFS) was 74·9% and 4-year overall survival (OS) was 86·3%, with a median follow-up period of 48·9 months. Of 11 patients without CNS involvement, 1 had CNS relapse and 3 intraocular relapse, and 4-year PFS and OS was 72·7% and 88·9%, respectively. Although white matter abnormalities shown by MRI were significantly increased at 4 years after rdWBRT, only one patient developed mild cognitive impairment. The combination of intravitreal chemotherapy, prophylactic systemic chemotherapy and rdWBRT for primary IOL showed a potential to reduce CNS relapse rate and improved 4-year PFS and OS without increase of cognitive dysfunction.

摘要

原发性眼内淋巴瘤(IOL)在初次诊断后的2年内有中枢神经系统(CNS)复发的倾向,这会影响临床结局。为降低CNS复发率,我们对有或无新诊断CNS受累的B细胞原发性IOL患者,采用了玻璃体内注射甲氨蝶呤、基于甲氨蝶呤的全身诱导化疗、巩固性大剂量阿糖胞苷以及减量全脑放射治疗(rdWBRT,23.4 Gy)的联合治疗方案。所有患者均接受了纵向脑磁共振成像(MRI)和认知评估,以评估治疗引起的白质脑病。17例患者开始并16例完成了方案治疗。2例患者发生CNS复发,3例发生眼内复发。4年无进展生存期(PFS)为74.9%,4年总生存期(OS)为86.3%,中位随访期为48.9个月。在11例无CNS受累的患者中,1例发生CNS复发,3例发生眼内复发,4年PFS和OS分别为72.7%和88.9%。尽管rdWBRT后4年MRI显示的白质异常显著增加,但只有1例患者出现轻度认知障碍。玻璃体内化疗、预防性全身化疗和rdWBRT联合用于原发性IOL显示出降低CNS复发率的潜力,并改善了4年PFS和OS,且未增加认知功能障碍。

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