原发性中枢神经系统淋巴瘤,治疗结果 - 10 年经验。单中心研究。

Ajla Nizic, Lejla Ibricevic-Balic, Timur Ceric, Ibrahim Omerhodzic, Lejla Burazerovic, Vasvija Saric, Emina Mameledzija, Berina Hasanefendic
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引用次数: 0

摘要

背景:原发性中枢神经系统淋巴瘤(PCNSL原发性中枢神经系统淋巴瘤(PCNSL)是一种侵袭性、罕见的非霍奇金淋巴瘤,其特点是无全身性疾病。关于 PCNSL 的治疗,目前数据有限,也没有严格定义的指南:本研究的目的是报告 PCNSL 治疗的 10 年经验,评估治疗效果以及这些患者的无进展生存期和总生存期:研究于 2012 年 1 月至 2022 年 12 月在波黑萨拉热窝大学临床中心血液学诊所进行。共有 24 名患者被纳入样本。所有患者均接受过诊断性手术。患者接受了基于大剂量甲氨蝶呤的治疗方案,同时接受/不接受全脑放疗作为巩固治疗。治疗反应通过成像技术来捕捉。通过影像学技术对复发患者进行评估,并根据基于甲氨蝶呤的治疗方案进行治疗:结果:我们采集到了平等的性别分布。患者的中位年龄为 59.5 岁(20-79 岁)。病理组织学分析证实,22 名患者确诊为 DLBCL,1 名患者确诊为 T 细胞淋巴瘤和无性大细胞淋巴瘤。5、18和1名患者分别接受了化疗、化疗联合WBRT和放疗。总完全反应率(CR)为 87.15%。接受联合模式治疗的患者的完全缓解率(CR)高于接受化疗的患者(94.4% 对 60%)。在24名患者中,有11人复发。复发的中位时间为29个月(从1个月到105个月)。二线治疗后,CR 为 54.5%,45.45% 的患者在治疗期间死亡。4名患者第二次复发,中位复发时间为9个月(从2个月到77个月)。2年的OS率为67%,中位OS率为45.9个月。2年的PFS率为31%:OS和PFS率表明,PCNSL患者使用新药和自体干细胞移植巩固治疗,可获得更好的治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Central Nervous System Lymphoma, Treatment Outcomes - 10 Year Experience. Single Center Study.

Background: Primary central nervous system lymphoma(PCNSL) is an aggressive, rare form of Non-Hodgkin lymphoma, characterized by the absence of systemic disease. There are limited data and no strictly defined guidelines for management of PCNSL.

Objective: The aim of this study was to report a 10 year experience of PCNSL treatment, to evaluate treatment outcomes and asses Progression Free and Overall Survival of these patients.

Methods: Study was conducted on the Haematology Clinic, Clinical center University of Sarajevo, BH, in the period from January 2012.-December 2022. Total sample of 24 patients were enrolled. All have undergone diagnostic surgery. Patients were treated with regimens based on High dose Methotrexate, with/without whole brain radiotherapy as consolidation. Treatment response was captured by imaging techniques. Patients who have relapsed were evaluated with imaging techniques and treated according to Methotrexate-based treatment protocols.

Results: We have captured equal gender distribution. The median age of patients was 59.5 years (range 20-79). Pathohistological analysis confirmed DLBCL diagnosis in 22 patients, T cell lymphoma and anaplastic large cell lymphoma, each in 1 patient. Chemotherapy, chemotherapy combined with WBRT and radiotherapy were given to 5, 18 and 1 patients, respectively. The overall complete response rate (CR) was 87,15%. Those receiving combined modality-treatment had higher CR than those receiving chemotherapy (94,4% versus 60%). Out of 24 patients, 11 of them relapsed. The median time to relapse was 29 months (from 1 to 105). After second line of the treatment, CR was 54,5%, while 45,45% of patients died during the treatment. 4 patients relapsed for the second time with median time to relapse of 9 months (from 2 to 77). 2 year OS rate was 67%, and the median OS rate was 45,9 months. 2 year PFS rate was 31%.

Conclusion: The OS and PFS rates indicate the usage of new drugs and consolidation with autologous stem cell transplantation in patients with PCNSL in order to achieve better treatment outcomes.

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