...
首页> 外文期刊>Cancer science. >Prognostic impact of immunohistochemical biomarkers in diffuse large B-cell lymphoma in the rituximab era.
【24h】

Prognostic impact of immunohistochemical biomarkers in diffuse large B-cell lymphoma in the rituximab era.

机译:免疫组化生物标志物在利妥昔单抗时代对弥漫性大B细胞淋巴瘤的预后影响。

获取原文
获取原文并翻译 | 示例

摘要

We evaluated the usefulness of prognostic markers in patients with diffuse large B-cell lymphoma (DLBCL) treated with cyclophosphamide, vincristine, doxorubicin, and prednisolone (CHOP) +/- rituximab (R-CHOP) in Japan. We studied 730 patients with DLBCL; 451 received CHOP and 279 R-CHOP. We analyzed biopsy samples immunohistochemically for markers of germinal center B cells (CD10, Bcl-6), postgerminal center B cells (Multiple myeloma-1), and apoptosis (Bcl-2). The median follow-up period for surviving patients was 56.4 months for the CHOP group and 25.2 months for the R-CHOP group. DLBCL were categorized as germinal center B (GCB) subtype (352/730; 48.2%) or non-GCB subtype (378/730; 51.8%). In the CHOP group, the high expression of CD10 (P = 0.022) or Bcl-6 (P = 0.021), or GCB subtype (P = 0.05) was associated with better overall survival, whereas the high expression of Bcl-2 (P = 0.001) or MUM1 (P = 0.011), or non-GCB subtype (P = 0.05) was associated with worse overall survival. In the R-CHOP group, however, these biomarkers except Bcl-6 were not significant prognostic factors. The patients with non-GCB subtype showed improved survival in the R-CHOP group (P = 0.756). The International Prognostic Index was a useful clinical marker of survival in the CHOP group (P < 0.001) and also in the R-CHOP group (P < 0.001). Results of improved survival with rituximab addition indicate that the relevance of previously recognized prognostic factors should be re-evaluated.
机译:我们在日本评估了用环磷酰胺,长春新碱,阿霉素和泼尼松龙(CHOP)+/-利妥昔单抗(R-CHOP)治疗的弥漫性大B细胞淋巴瘤(DLBCL)患者的预后指标的有效性。我们研究了730例DLBCL患者; 451人获得了CHOP,279人获得了R-CHOP。我们通过免疫组织化学分析了活检样本中生发中心B细胞(CD10,Bcl-6),发芽后中心B细胞(多发性骨髓瘤1)和凋亡(Bcl-2)的标志物。 CHOP组存活患者的中位随访期为56.4个月,R-CHOP组为25.2个月。 DLBCL分为生发中心B(GCB)亚型(352/730; 48.2%)或非GCB亚型(378/730; 51.8%)。在CHOP组中,CD10(P = 0.022)或Bcl-6(P = 0.021)或GCB亚型(P = 0.05)的高表达与更好的总体生存率相关,而Bcl-2(P = 0.001)或MUM1(P = 0.011)或非GCB亚型(P = 0.05)与较差的总体生存率相关。然而,在R-CHOP组中,除了Bcl-6以外,这些生物标志物都不是重要的预后因素。非GCB亚型的患者在R-CHOP组中表现出更好的生存率(P = 0.756)。国际预后指数是CHOP组(P <0.001)和R-CHOP组(P <0.001)存活的有用临​​床标志。添加利妥昔单抗改善生存率的结果表明,应重新评估先前公认的预后因素的相关性。

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