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De novo CD5+diffuse large B-cell lymphoma, NOS: clinical characteristics and outcomes in rituximab era

机译:De Novo CD5 + Diffuse大B细胞淋巴瘤,NoS:Rituximab时代的临床特征和结果

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摘要

CD5+ diffuse large B-cell lymphoma (DLBCL), NOS represents a distinct subset of DLBCL associated with poorer outcomes and extranodal disease. We analyzed characteristics and outcomes for 102 CD5+ DLBCL patients diagnosed between 2001-2016. The majority had poor-risk disease based on R-IPI scores; 80% had extranodal disease at diagnosis. CNS relapse occurred 23% of the time. Median PFS and OS was 18.9 months and 112 months, respectively. Four-year PFS rates were 100%, 53%, and 41% for patients with R-IPI scores of very good, good, and poor, respectively. CD5+ DLBCL represents a subset of patients with poor outcomes despite rituximab and anthracycline-based regimens. There is a need for novel therapies and clinical trials for this high-risk group of patients. Given high rates of CNS relapse, better CNS prophylaxis with frontline therapy requires more study.
机译:CD5 +弥漫性大B细胞淋巴瘤(DLBCL),NoS表示与较差的结果和外骨疾病相关的DLBCL不同的子集。 我们分析了诊断为2001 - 2016年诊断的102例CD5 + DLBCL患者的特征和结果。 大多数基于R-IPI分数患风险差; 80%的诊断患有外骨病。 CNS复发发生了23%的时间。 中位数PFS和OS分别为18.9个月和112个月。 对于R-IPI评分分别非常好,良好,差的患者,四年的PFS率为100%,53%和41%。 尽管有利妥昔单抗和基于蒽环类的方案,CD5 + DLBCL代表了患者的患者患者。 需要对这种高风险患者组进行新的疗法和临床试验。 鉴于CNS复发的高率,具有前线疗法的更好的CNS预防需要更多的研究。

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