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首页> 外文期刊>BMC Cancer >MYC and BCL2 overexpression is associated with a higher class of Memorial Sloan-Kettering Cancer Center prognostic model and poor clinical outcome in primary diffuse large B-cell lymphoma of the central nervous system
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MYC and BCL2 overexpression is associated with a higher class of Memorial Sloan-Kettering Cancer Center prognostic model and poor clinical outcome in primary diffuse large B-cell lymphoma of the central nervous system

机译:MYC和BCL2过表达与纪念斯隆-凯特琳癌症中心的较高预后模型和中枢神经系统原发性弥漫性大B细胞淋巴瘤的临床预后不良相关

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摘要

Background Primary diffuse large B-cell lymphoma of the central nervous system (PCNS-DLBCL) is a distinct clinicopathological entity with a poor prognosis. Concurrent MYC and BCL2 overexpression predicts inferior prognosis in systemic DLBCLs. However, the prognostic significance of MYC and BCL2 in PCNS-DLBCL remains elusive. Methods Immunohistochemistry (IHC) of MYC, BCL2 and BCL6 was performed on tumor samples from 114 patients with PCNS-DLBCL. IHC score was assigned based on the proportion of immunostained cells. Results MYC, BCL2, and BCL6 IHC scores were 18.16?±?19.58, 58.86?±?35.07, and 39.39?±?37.66?% (mean?±?SD), respectively. Twenty-one cases (18.1?%) were designated as MYC-positive with a cutoff score of 40. BCL2 positivity was found in 87 cases (75.0?%) using a cutoff score of 30. MSKCC (Memorial Sloan-Kettering Cancer Center prognostic model) class 2 and 3 had higher rates of MYC and/or BCL2 positivity (MYC, P =?0.012; BCL2, P =?0.008; dual-positive, P =?0.022). Poor KPS (Karnofsky Performance Status score 60?years) showed poorer overall survival (OS) ( P =?0.020). MYC positivity was associated with poor PFS ( P =?0.027), while patients with BCL2 positivity exhibited a shorter OS ( P =?0.010). Concomitant MYC and BCL2 positivity was related to poor PFS ( P =?0.041), while the lack of both MYC and BCL2 expression was related to prolonged OS ( P =?0.014). MYC and BCL2 expression had no independent prognostic implication by multivariate analysis in overall patients with PCNS-DLBCL. However, among patients treated with combined high-dose methotrexate, vincristine and procarbazine and radiotherapy, dual MYC and BCL2 overexpression (a cutoff score of 60) was an independent poor prognostic indicator ( P =?0.010). Conclusions Evaluation of MYC and BCL2 expression may be helpful for the determination of PCNS-DLBCL prognosis.
机译:背景原发性中枢神经系统弥漫性大B细胞淋巴瘤(PCNS-DLBCL)是预后较差的独特临床病理学实体。同时MYC和BCL2过表达预测系统性DLBCL的预后较差。然而,MYC和BCL2在PCNS-DLBCL中的预后意义仍然难以捉摸。方法对114例PCNS-DLBCL患者的肿瘤标本进行MYC,BCL2和BCL6的免疫组化分析。 IHC评分是根据免疫染色细胞的比例分配的。结果MYC,BCL2和BCL6 IHC得分分别为18.16?±?19.58、58.86?±?35.07和39.39?±?37.66?%(平均值?±?SD)。 21例(18.1%)被指定为MYC阳性,截断评分为40。BCL2阳性发现87例(75.0%),截断评分为30。MSKCC(Memorial Sloan-Kettering Cancer Center)预后2型和3级具有较高的MYC和/或BCL2阳性率(MYC,P = 0.012; BCL2,P = 0.008;双阳性,P = 0.022)。 KPS差(Karnofsky绩效状态评分为60?年)显示总体生存率(OS)较差(P =?0.020)。 MYC阳性与较差的PFS相关(P =?0.027),而BCL2阳性的患者的OS较短(P =?0.010)。 MYC和BCL2阳性与PFS差有关(P =?0.041),而MYC和BCL2表达的缺乏与OS延长有关(P =?0.014)。通过多变量分析,在全部PCNS-DLBCL患者中,MYC和BCL2表达没有独立的预后含义。然而,在接受大剂量甲氨蝶呤,长春新碱和卡巴嗪联合放疗的患者中,双重MYC和BCL2过表达(临界值为60)是独立的不良预后指标(P = 0.010)。结论评价MYC和BCL2表达可能有助于确定PCNS-DLBCL的预后。

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