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