首页> 外文期刊>Human Pathology >p53 expression in large B-cell lymphomas with MYC extra copies and CD99 expression in large B-cell lymphomas in relation to MYC status
【24h】

p53 expression in large B-cell lymphomas with MYC extra copies and CD99 expression in large B-cell lymphomas in relation to MYC status

机译:P53大型B细胞淋巴瘤的表达与Myc额外拷贝和CD99表达在大型B细胞淋巴瘤中,与MYC状态相关

获取原文
获取原文并翻译 | 示例
           

摘要

p53 expression and MYC extra copies (MYC-EC) have been reported to serve as independent adverse prognostic markers in patients with diffuse large B-cell lymphoma (DLBCL). However, the impact of p53 expression in MYC-EC lymphomas has not been delineated. Conversely, CD99 expression has been shown to have a positive impact on survival in patients with germinal center-type DLBCL, yet nothing is reported about the impact of CD99 expression and MYC status. This is the first study to evaluate p53 expression in MYC-EC lymphomas and CD99 expression in relation to MYC status. We identified 122 patients diagnosed as having large B-cell lymphoma (44, MYC-negative; 29, MYC-EC; 23, MYC rearrangement; 22, MYC and BCL2 rearrangements; 4, MYC, BCL2, and BCL6 rearrangements). p53 expression significantly correlated with DLBCL with abnormal MYC status (MYC-EC, MYC rearrangement, and MYC overexpression), but adverse p53 prognostic effect was only seen with MYC-rearranged lymphoma. CD99 expression was significantly associated with MYC-negative DLBCL and had better prognostic impact on lymphoma-specific survival (LSS), but not on relapse-free survival and overall survival. Overall, patients with MYC-EC lymphoma had significantly worse relapse-free survival and LSS than did patients with MYC-negative lymphoma, yet better overall survival and LSS than did the patients with MYC-rearranged lymphoma. Thus, patients with MYC-EC lymphomas had prognostic features that were intermediate between MYC-negative and MYC-rearranged lymphomas. Lastly, high-intensity chemotherapy (either dose-adjusted rituximab and etoposide-prednisone-vincristine-cyclophosphamide-doxorubicin or rituximab and hyperfractionated cyclophosphamide-vincristine-doxorubicin-dexamethasone treatment) did not improve survival in patients with MYC-EC and MYC-rearranged lymphoma when compared with rituximab-cyclophosphamide-hydroxydaunomycin-vincristine-prednisone therapy. (C) 2018 Elsevier Inc. All rights reserved.
机译:据报道,P53表达和MYC额外拷贝(MYC-EC)用作弥漫性大B细胞淋巴瘤(DLBCL)患者的独立不良预后标志物。然而,P53表达在Myc-EC淋巴瘤中的影响尚未划定。相反,已显示CD99表达对生发中心型DLBCL患者的生存产生积极影响,但没有据报道CD99表达和MYC状态的影响。这是第一次评估Myc-EC淋巴瘤和CD99表达的P53表达与MYC状态相关的研究。我们鉴定了122名诊断为具有大B细胞淋巴瘤的患者(44,Myc-Digal; 29,Myc-EC; 23,Myc重排; 22,Myc和Bcl2重排; 4,Myc,Bcl2和Bcl6重排)。 P53表达与DLBCL具有异常MYC状态(MYC-EC,MYC重新排列和MYC过表达)显着相关,但仅通过MYC重新排列的淋巴瘤看到不良P53预后效果。 CD99表达与Myc阴性DLBCL显着相关,对淋巴瘤特异性生存(LSS)具有更好的预后影响,但不具有无复发存活和整体存活。总体而言,患有Myc-EC淋巴瘤的患者显着更严重的复发存活和LSS,而不是Myc阴性淋巴瘤的患者,但总体存活率和LSS比患有Myc重新排列的淋巴瘤的患者。因此,Myc-EC淋巴瘤的患者具有预后的特征,其在Myc阴性和Myc重新排列的淋巴瘤之间是中间体。最后,高强度化疗(剂量调节的Rituximab和Etoposide-prednisone-vincristine-环膦酰胺或Rituximab和Hyperucated环磷酰胺-Vincristine-doxorubiCin-甲酰胺处理)并未改善Myc-EC和Myc重排淋巴瘤患者的存活与Rituximab-环膦酰胺 - 羟基霉素 - 血管霉素 - 泼尼松治疗相比。 (c)2018年Elsevier Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号