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Cytogenetic studies and their prognostic contribution in 565 Chinese patients with primary myelofibrosis.

机译:细胞遗传学研究及其对565名中国原发性骨髓纤维化患者的预后影响。

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摘要

To study the feature and prognostic contribution of cytogenetic information in Chinese patients with primary myelofibrosis (PMF), we analyzed cytogenetic data from 565 patients with PMF. One hundred and sixty-two subjects (29%) had abnormal karyotypes, including trisomy 8 (45; 28%), deletion of 20q (25; 15%), deletion of 13q (13; 8%), deletion of 11q (12; 7%), and abnormal chromosome 1 (21; 13%); balanced translocations (14; 9%); a complex karyotype (CK; 30; 19%), and a monosomal karyotype (MK; 19; 12%). Using these data, we showed that the Dynamic International Prognostic Scoring System (DIPSS)-plus, which includes cytogenetic information, is a better survival predictor than the DIPSS. We next used our data to construct the following two cytogenetic-based cohorts: (1) favorable karyotype-subjects with a normal karyotype, a CK that is not a MK, +8 only or a balanced translocation only and (2) unfavorable karyotype-all others. The median survival times were not reached and were 52 month (95% CI, 32-72 months; P?=?0.01) in patients with favorable and unfavorable karyotypes, respectively. These data provided the detailed cytogenetic information in Chinese patients with PMF and confirmed the impact of cytogenetic abnormalities on survival in Chinese patients.
机译:为了研究中国原发性骨髓纤维化(PMF)患者细胞遗传学信息的特征和预后,我们分析了565例PMF患者的细胞遗传学数据。 162名受试者(29%)的核型异常,包括三体性8(45; 28%),缺失20q(25; 15%),缺失13q(13; 8%),缺失11q(12 ; 7%)和1号染色体异常(21; 13%);平衡易位(14; 9%);复杂的核型(CK; 30; 19%)和单体核型(MK; 19; 12%)。使用这些数据,我们表明,动态国际预后评分系统(DIPSS)-plus(包括细胞遗传学信息)比DIPSS更好地预测生存。接下来,我们使用我们的数据构建了以下两个基于细胞遗传学的队列:(1)具有正常核型,非MK的CK,仅+8或仅平衡易位的CK核型,以及(2)不利的核型所有其他人。有利和不利核型患者的中位生存时间均未达到,分别为52个月(95%CI,32-72个月;P≥0.01)。这些数据提供了中国PMF患者的详细细胞遗传学信息,并证实了细胞遗传学异常对中国患者生存的影响。

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