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首页> 外文期刊>Leukemia and lymphoma >Retrospective analysis of 235 unselected patients with mantle cell lymphoma confirms prognostic relevance of Mantle Cell Lymphoma International Prognostic Index and Ki-67 in the era of rituximab: long-term data from the Czech Lymphoma Project Database.
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Retrospective analysis of 235 unselected patients with mantle cell lymphoma confirms prognostic relevance of Mantle Cell Lymphoma International Prognostic Index and Ki-67 in the era of rituximab: long-term data from the Czech Lymphoma Project Database.

机译:对235例未选择的套细胞淋巴瘤患者的回顾性分析证实了利妥昔单抗时代套细胞淋巴瘤国际预后指数和Ki-67的预后相关性:来自捷克淋巴瘤项目数据库的长期数据。

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摘要

Although a prognostic model (MIPI, Mantle Cell Lymphoma International Prognostic Index) for patients with mantle cell lymphoma (MCL) has been established, its clinical significance for daily practice in the rituximab era remains controversial. Data of 235 unselected patients with MCL from the Czech Lymphoma Project Database were analyzed. MIPI, simplified MIPI (s-MIPI) and Ki-67 proliferation index were assessed for all patients and for a subgroup of 155 rituximab-treated (RT) patients. MIPI divided all patients into subgroups of low-risk (22%), intermediate-risk (29%) and high-risk (49%), with median overall survival 105.8 vs. 54.1 vs. 24.6 months, respectively (p < 0.001). s-MIPI revealed similar results. The validity of both indexes was confirmed in RT patients. We confirmed the Ki-67 index to be a powerful single prognostic factor for overall survival (64.4 vs. 20.1 months, p < 0.001) for all patients and for the RT subset. Our results confirm the clinical relevance of MIPI, s-MIPI and Ki-67 for risk stratification in MCL also in the rituximab era.
机译:尽管已经建立了套细胞淋巴瘤(MCL)患者的预后模型(MIPI,套细胞淋巴瘤国际预后指数),但其在利妥昔单抗时代日常实践中的临床意义仍存在争议。分析了来自捷克淋巴瘤项目数据库的235名未选出的MCL患者的数据。对所有患者以及155名接受利妥昔单抗(RT)治疗的患者亚组评估MIPI,简化MIPI(s-MIPI)和Ki-67增殖指数。 MIPI将所有患者分为低危(22%),中危(29%)和高危(49%)亚组,中位总生存期分别为105.8、54.1和24.6个月(p <0.001) 。 s-MIPI显示了相似的结果。这两项指标在RT患者中均有效。我们证实Ki-67指数是所有患者和RT子集总体生存的有力预后因素(64.4 vs. 20.1个月,p <0.001)。我们的结果证实了在利妥昔单抗时代,MIPI,s-MIPI和Ki-67与MCL风险分层的临床相关性。

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