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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例外壳细胞淋巴瘤患者的回顾性分析证实了人妖细胞淋巴瘤国际预后指数和KI-67在RITUXIMAB时代的预后相关性: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:虽然已经建立了伴细胞淋巴瘤(MCL)患者的预后模型(MIPI,MIPI,MIPI,MIPI,MIPI,MPL),但其日常生活中的日常行进患者仍存在争议。分析了来自捷克淋巴瘤项目数据库235例未选择的MCL患者的数据。为所有患者和155例Rituximab治疗(RT)患者的亚组评估MIPI,简化的MIPI(S-MIPI)和KI-67增殖指数。 MIPI将所有患者分为低风险(22%),中间风险(29%)和高风险(49%)的亚组分别,中位数总存活105.8与54.1与24.6个月(P <0.001) 。 S-MIPI揭示了类似的结果。在RT患者中确认了两种指标的有效性。我们证实了KI-67指数为所有患者的整体存活(64.4与20.1个月,P <0.001)的强大单一预后因素,以及RT子集。我们的结果证实了MIPI,S-MIPI和KI-67在Rituximab时代的MCL中风险分层的临床相关性。

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