Primary Central Nervous System Lymphomas: A Single-Center Experience.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Medical Bulletin of Sisli Etfal Hospital Pub Date : 2025-03-18 eCollection Date: 2025-01-01 DOI:10.14744/SEMB.2025.24022
Sidika Gulkan Ozkan, Seyedehtina Safaei, Ali Kimiaei, Zeynep Asli Durak, Mehmet Serdar Yildiz, Yuksel Asli Ozturkmen, Hasan Atilla Ozkan
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引用次数: 0

Abstract

Objectives: Primary central nervous system lymphoma (PCNSL) is a rare and aggressive form of non-Hodgkin lymphoma (NHL). This study aimed to investigate the characteristics, treatment approaches, and outcomes of patients with PCNSL in a single institution.

Methods: We retrospectively analyzed 11 patients with PCNSL treated at our institution between October 2022 and July 2024. Patient demographics, clinical characteristics, treatment modalities, and outcomes were evaluated.

Results: The median age of the patients was 65 years, with male predominance (63.64%). The median follow-up duration was 10 months. All patients were immunocompetent, and 90.91% had diffuse large B-cell lymphoma. At diagnosis, 81% of the patients were considered fit to receive HDMTX treatment. R-MPV was the most common first-line treatment (45.45%). The complete response rate to initial treatment was 80%. The treatment-related mortality was 9.09%. Autologous stem cell transplantation (ASCT) was performed in 72.73% of the patients, with rituximab-thiotepa-carmustine as the predominant conditioning regimen (62.50%). Treatment-related toxicities occurred in 50% of patients, and 87.50% of patients experienced transplant-related complications. The transplantation-related mortality rate was 25%. The relapse rate was 25% among the patients undergoing ASCT. The mortality rate was 36.36%, and cerebellar involvement was significantly associated with a higher mortality rate (p=0.045).

Conclusion: This study demonstrated the efficacy of methotrexate-based regimens and ASCT in the treatment of PCNSL and achieved high complete response rates. However, the significant incidence of treatment-related toxicities and mortality underscores the persistent challenges of managing this disease. In addition, the association between cerebellar involvement and increased mortality requires further investigation. Larger prospective studies are needed to validate these findings.

原发性中枢神经系统淋巴瘤:单中心经验。
目的:原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见的侵袭性非霍奇金淋巴瘤(NHL)。本研究旨在调查单一机构中PCNSL患者的特征、治疗方法和预后。方法:回顾性分析2022年10月至2024年7月在我院治疗的11例PCNSL患者。评估患者人口统计学、临床特征、治疗方式和结果。结果:患者中位年龄65岁,男性居多(63.64%)。中位随访时间为10个月。所有患者免疫功能正常,90.91%为弥漫性大b细胞淋巴瘤。在诊断时,81%的患者被认为适合接受HDMTX治疗。R-MPV是最常见的一线治疗(45.45%)。初始治疗的完全缓解率为80%。治疗相关死亡率为9.09%。72.73%的患者进行了自体干细胞移植(ASCT),以利妥昔单抗-硫替帕-卡莫司汀为主要治疗方案(62.50%)。50%的患者出现治疗相关毒性,87.50%的患者出现移植相关并发症。移植相关死亡率为25%。接受ASCT的患者复发率为25%。死亡率为36.36%,小脑受累与较高的死亡率显著相关(p=0.045)。结论:本研究证明了甲氨蝶呤为主的方案和ASCT治疗PCNSL的有效性,并取得了较高的完全缓解率。然而,与治疗相关的毒性和死亡率的显著发生率强调了管理这种疾病的持续挑战。此外,小脑受累与死亡率增加之间的关系需要进一步调查。需要更大规模的前瞻性研究来验证这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medical Bulletin of Sisli Etfal Hospital
Medical Bulletin of Sisli Etfal Hospital MEDICINE, GENERAL & INTERNAL-
自引率
16.70%
发文量
41
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