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年轻侵袭性 B 细胞淋巴瘤患者的中枢神经系统疾病:Mabthera 国际试验和德国高级非霍奇金淋巴瘤研究组试验中患者的分析。

CNS disease in younger patients with aggressive B-cell lymphoma: an analysis of patients treated on the Mabthera International Trial and trials of the German High-Grade Non-Hodgkin Lymphoma Study Group.

机构信息

Department of Hematology, Oncology and Stem Cell Transplantation, Asklepios Hospital St. Georg, Hamburg.

Institute for Medical Informatics, Statistics and Epidemiology (IMISE), University of Leipzig, Leipzig.

出版信息

Ann Oncol. 2012 May;23(5):1267-1273. doi: 10.1093/annonc/mdr440. Epub 2011 Oct 11.

Abstract

BACKGROUND

To describe incidence, risk factors, and influence of treatment on occurrence of central nervous system (CNS) relapse or progression in younger patients with aggressive B-cell lymphoma.

PATIENTS AND METHODS

We analyzed 2210 patients with aggressive B-cell lymphoma treated on various studies for CNS relapse/progression. Treatment consisted of CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone) ± etoposide. Six hundred and twenty patients also received rituximab. CNS prophylaxis was intrathecal methotrexate on High-CHOEP and MegaCHOEP phase III studies if upper neck, head, bone marrow, or testes were involved.

RESULTS

Fifty-six of 2196 patients (2.6%) developed CNS disease. It occurred early (median 7.0 months), median survival was 5.0 months. Patients with age-adjusted International Prognostic Index (aaIPI) 0 or 1 treated with rituximab showed a low risk for CNS disease (2-year rates: 0% or 0.5%), and rituximab decreased the risk (relative risk 0.3, 95% confidence interval 0.1-0.9, P = 0.029). Patients with aaIPI 2 or 3 showed a moderate risk (4.2%-9.7%) and no significant reduction of CNS disease with rituximab. CNS prophylaxis was of no significant benefit.

CONCLUSIONS

In younger patients with aaIPI 0 or 1, CNS relapse/progression is very rare; in patients with aaIPI 2 or 3, the risk is higher (up to 10%) and requires new diagnostic strategies and treatment.

摘要

背景

描述侵袭性 B 细胞淋巴瘤年轻患者中枢神经系统(CNS)复发或进展的发生率、风险因素和治疗影响。

患者和方法

我们分析了在不同研究中接受 CNS 复发/进展治疗的 2210 例侵袭性 B 细胞淋巴瘤患者。治疗包括 CHOP(环磷酰胺、多柔比星、长春新碱和泼尼松)±利妥昔单抗。620 例患者还接受了利妥昔单抗治疗。如果上颈部、头部、骨髓或睾丸受累,则在上颈、头、骨髓或睾丸受累时,在 High-CHOEP 和 MegaCHOEP III 研究中采用鞘内甲氨蝶呤进行 CNS 预防。

结果

2196 例患者中有 56 例(2.6%)发生 CNS 疾病。它发生较早(中位时间 7.0 个月),中位生存时间为 5.0 个月。年龄调整后的国际预后指数(aaIPI)为 0 或 1 且接受利妥昔单抗治疗的患者,CNS 疾病风险较低(2 年发生率:0%或 0.5%),利妥昔单抗降低了风险(相对风险 0.3,95%置信区间 0.1-0.9,P=0.029)。aaIPI 为 2 或 3 的患者,风险中等(4.2%-9.7%),且利妥昔单抗不能显著降低 CNS 疾病的风险。CNS 预防无显著获益。

结论

在 aaIPI 为 0 或 1 的年轻患者中,CNS 复发/进展非常罕见;在 aaIPI 为 2 或 3 的患者中,风险更高(高达 10%),需要新的诊断策略和治疗。

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