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Mesenchymal stromal cell density is increased in higher grade myelodysplastic syndromes and independently predicts survival.

在高级别的骨髓增生异常综合征中,间充质基质细胞的密度增加,并且能独立预测生存时间。

Johnson RC,Kurzer JH,Greenberg PL,Gratzinger D

Abstract

We retrospectively tested the prognostic and diagnostic significance of CD271+ mesenchymal stromal cell (MSC) density in cytopenic patients who underwent bone marrow biopsy to evaluate for myelodysplastic syndromes (MDS).
CD271+ MSC density was quantitated by automated image analysis of tissue microarray cores in 125 cytopenic patients: 40 lower grade MDS (<5% marrow blasts), 24 higher grade MDS, and 61 benign.
CD271+ MSC density was increased in higher grade MDS compared with benign (P = .006) and lower grade MDS (P = .02). CD271+ MSC density was predictive of survival among patients with MDS independent of Revised International Prognostic Scoring System (IPSS-R), history of transfusion, therapy-related MDS, and fibrosis (hazard ratio, 3.4; P < .001). Among low or intermediate IPSS-R patients, median survival was significantly shorter in the high CD271+ MSC density group (47 vs 18 months, P < .02).
High CD271+ MSC density is characteristic of higher grade MDS and is associated with poor risk independent of known prognostic factors.

摘要

我们回顾性检查了CD271+间充质基质细胞(MSC)密度在接受骨髓活检以评估骨髓增生异常综合征(MDS)的血细胞减少症患者中的诊断和预后意义。
通过对125例血细胞减少症患者的组织芯片自动图像分析进行CD271+MSC密度定量检查:包括40例低级别的MDS(<5%的骨髓原始细胞),24例高级别的MDS和61例良性MDS。
与良性MDS(P=0.006)和低级别MDS(P=0.02)相比,高级别MDS的CD271+MSC密度增加。CD271+MSC密度对MDS患者生存时间预测的影响独立于修订国际预后评分系统(IPSS-R)、输血史、治疗相关的MDS和纤维化(危险比,3.4;P<0.001)。在低或中等IPSS-R的患者中,中位生存时间显着短于高CD271+MSC密度组(47vs18个月,P<0.02)。
高CD271+MSC密度是高级别MDS的特征,并独立于已知的预后因素,与较差的预后相关。

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