原发性中枢神经系统淋巴瘤的临床结局和治疗模式:多中心回顾性分析

Serkan Guven
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Results: The median age of the patients was 59 (min.: 22, max.: 78) years. The male-to-female ratio was 1.26/1. Nineteen (55.9%) patients had Eastern Cooperative Oncology Group (ECOG) performance score of ≥2. Fifteen (44.1%) patients had normal lactate dehydrogenase (LDH) levels and only 14.7% of the patients had B symptoms at the time of diagnosis. Magnetic resonance imaging (MRI) revealed a single mass lesion in 14 (41.2%) patients. As an induction therapy, meth-otrexate-based regimen was administered in 29 (85.3%) patients. Only 14 of the 34 patients received 4 or more cycles of high-dose methotrexate (MTX). About 32.4% of the patients received radiation therapy (RT) during follow-up as a part of induction therapy. Five patients received only RT due to poor performance status. Ibrutinib was administered in 5 patients for refractory disease. 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引用次数: 0

摘要

目的:原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见的恶性疾病,预后较差。它的低发病率给治疗决策带来了挑战。事实上,对于适当的治疗方式仍未达成共识。在这种背景下,本研究的目的是调查和比较评估几种治疗方式在治疗PCNSL中的疗效。方法:将2007年至2021年间在5个不同血液学中心诊断为PCNSL的34例患者纳入研究。回顾性收集所有五个中心的患者资料。由于伊鲁替尼在土耳其未被批准用于该适应症,因此需要获得每位患者的适应症外使用伊鲁替尼的同意。伦理委员会于2021年6月9日获得批准,决定号为2021/18-05。结果:患者中位年龄59岁(最小22岁,最大22岁)。: 78岁。男女比例为1.26/1。东部肿瘤合作组(ECOG)评分≥2分19例(55.9%)。15例(44.1%)患者乳酸脱氢酶(LDH)水平正常,诊断时仅有14.7%的患者有B症状。磁共振成像(MRI)显示14例(41.2%)患者有单一肿块病变。作为诱导治疗,29例(85.3%)患者接受了以甲氨蝶呤为基础的方案。34例患者中只有14例接受了4个或更多周期的高剂量甲氨蝶呤(MTX)治疗。约32.4%的患者在随访期间接受放射治疗(RT)作为诱导治疗的一部分。5例患者因表现不佳仅接受RT治疗。5例难治性疾病患者给予依鲁替尼治疗。确定四个或更多周期的MTX治疗可增加无进展生存期(PFS) (p=0.031)和总生存期(OS) (p=0.012)。此外,RT改善PFS (p=0.023)。考虑到诱导治疗获得的完全缓解影响长期生存,获得最佳的治疗方案与新药物联合使用可能延长生存期(PFS: p=0.01, OS: p=0.023)。结论:本研究结果表明,治疗的初始反应是至关重要的。此外,发现高剂量MTX治疗应给予4个周期或更长时间,以达到最佳效果。此外,确定伊鲁替尼单药治疗在复发/难治性疾病患者中耐受性良好,具有出色的临床益处。总之,大剂量MTX、依鲁替尼和利妥昔单抗的联合治疗似乎是一种有希望的初始治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Outcomes and Treatment Patterns of Primary Central Nervous System Lymphoma: Multicenter Retrospective Analysis
Objectives: Primary central nervous system lymphoma (PCNSL) is a rare malignant disease with poor prognosis. Its low incidence leads to challenges in decision-making for treatment. As a matter of fact, there is still no consensus on the appropriate treatment modalities. In this context, the objective of this study is to investigate and comparatively assess the efficacies of several treatment modalities in the treatment of PCNSL. Methods: Thirty-four patients diagnosed with PCNSL at 5 different hematology centers between 2007 and 2021 were included in the study. Patients’ data from all five centers were collected retrospectively. Since ibrutinib is not approved for this indication in Turkey, consent for off-label use of ibrutinib is obtained from each patient. Ethics committee ap- proval was obtained on June 9, 2021 with decision number 2021/18-05. Results: The median age of the patients was 59 (min.: 22, max.: 78) years. The male-to-female ratio was 1.26/1. Nineteen (55.9%) patients had Eastern Cooperative Oncology Group (ECOG) performance score of ≥2. Fifteen (44.1%) patients had normal lactate dehydrogenase (LDH) levels and only 14.7% of the patients had B symptoms at the time of diagnosis. Magnetic resonance imaging (MRI) revealed a single mass lesion in 14 (41.2%) patients. As an induction therapy, meth-otrexate-based regimen was administered in 29 (85.3%) patients. Only 14 of the 34 patients received 4 or more cycles of high-dose methotrexate (MTX). About 32.4% of the patients received radiation therapy (RT) during follow-up as a part of induction therapy. Five patients received only RT due to poor performance status. Ibrutinib was administered in 5 patients for refractory disease. It was determined that four or more cycles of MTX treatment increased progression-free survival (PFS) (p=0.031) and overall survival (OS) (p=0.012). Moreover, RT improved PFS (p=0.023). Considering that the complete response achieved by induction therapy influences long-term survival, achievement of the best response to the treatment regimens administered in combination with new agents may prolong survival (PFS: p=0.01, OS: p=0.023). Conclusion: The findings of this study indicate that the initial response to treatment is crucial. Additionally, it was found that high-dose MTX treatment should be administered for 4 cycles or more in order to achieve the best results. Furthermore, it was determined that ibrutinib monotherapy was well-tolerated in our patients with relapsed/refractory disease, with excellent clinical benefits. In conclusion, a combination therapy consisting of high-dose MTX, ibrutinib, and rituximab appears to be a promising initial treatment approach in appropriate patients.
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