Relapse pattern and prognostic factors for patients with primary central nervous system lymphoma.

The Korean Journal of Hematology Pub Date : 2012-03-01 Epub Date: 2012-03-28 DOI:10.5045/kjh.2012.47.1.60
Jeong Eun Kim, Dok Hyun Yoon, Shin Kim, Dae Ho Lee, Jeong Hoon Kim, Young Hee Yoon, Hyun Sook Chi, Sang Wook Lee, Chan-Sik Park, Jooryung Huh, Cheolwon Suh
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引用次数: 18

Abstract

Background: Primary central nervous system lymphoma (PCNSL) rarely relapses in extracranial sites, and no specialized guidelines for follow-up evaluation have been proposed.

Methods: We analyzed 65 patients with newly diagnosed PNCSL to evaluate the pattern of relapse and prognostic factors.

Results: Of the 65 patients analyzed, 55 had only parenchymal brain disease, and 10 had both intracranial and extracranial lesions. As a first-line treatment, 29 patients received chemotherapy only (CTx), 13 received chemotherapy followed by whole brain radiotherapy (CTx-WBRT), 18 received chemotherapy followed by autologous stem cell transplantation (CTx-ASCT), 2 received palliative WBRT, and 3 received best supportive care. The overall response rate to the initial treatment was 75.8%, with specific response rates of 62.1% to CTx, 84.6% to CTx-WBRT, and 100% to CTx-ASCT. The complete response (CR) rate was higher with CTx-ASCT than in the absence of ASCT (77.8% vs. 43.2%; P=0.025). After a median follow-up of 18.8 months, the median failure-free survival (FFS) and overall survival (OS) were 13.0 and 36.1 months, respectively. No systemic relapse without a CNS lesion was noted. Multivariate analysis showed that ASCT was predictive of better FFS but not of OS. Age and the Memorial-Sloan Kettering Cancer Center prognostic score were predictive of survival.

Conclusion: We observed no systemic relapse without a CNS lesion, suggesting that regular systematic evaluation of extracranial sites may not always be necessary. Age was prognostic of survival irrespective of treatment scheme. ASCT may improve CR rate and FFS.

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原发性中枢神经系统淋巴瘤患者复发模式及预后因素分析。
背景:原发性中枢神经系统淋巴瘤(PCNSL)很少在颅外部位复发,没有专门的随访评估指南。方法:分析65例新诊断的PNCSL患者的复发模式及预后因素。结果:在分析的65例患者中,55例仅患有脑实质疾病,10例同时患有颅内和颅外病变。作为一线治疗,单纯化疗(CTx) 29例,化疗后全脑放疗(CTx-WBRT) 13例,化疗后自体干细胞移植(CTx- asct) 18例,姑息性WBRT 2例,最佳支持治疗3例。初始治疗的总有效率为75.8%,其中CTx特异性有效率为62.1%,CTx- wbrt特异性有效率为84.6%,CTx- asct特异性有效率为100%。CTx-ASCT组的完全缓解率(CR)高于未行ASCT组(77.8% vs. 43.2%;P = 0.025)。中位随访18.8个月后,中位无故障生存期(FFS)和总生存期(OS)分别为13.0和36.1个月。无系统性复发,无中枢神经系统病变。多因素分析显示,ASCT可预测更好的FFS,但不能预测OS。年龄和纪念斯隆凯特琳癌症中心的预后评分可以预测患者的生存。结论:我们未观察到无中枢神经系统病变的全身复发,提示定期系统评估颅外部位可能并不总是必要的。不论治疗方案如何,年龄是生存的预后因素。ASCT可提高CR率和FFS。
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