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Refractory cytopenia with unilineage dysplasia: analysis of prognostic factors and survival in 126 patients.

机译:难治性血细胞减少症伴单系增生:126例患者的预后因素和生存分析。

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According to the revised WHO classification of 2008, dysplasia in > or = 10% of one bone marrow lineage and one cytopenia constitutes the low-risk category of unilineage cytopenia and unilineage dysplasia (UCUD). We retrospectively reclassified, according to WHO, low-risk MDS from our database and found 126 subjects with these features at diagnosis: 79 patients were categorized as refractory anemia (RA), 23 patients as refractory neutropenia (RN), and 24 as refractory thrombocytopenia (RT). We did not find differences between the three subgroups as regards sex, median age, and cytogenetic aberrations. Lower PMN count (0.8 x 10(9)/L) was observed in the RN category, as well as lower platelet count in the RT category (51 x 10(9)/L). Moreover, we found a lower rate of patients requiring RBC transfusions, during the disease course, in the RT category (45.8%) as compared to RA (62%) and RN (69%) groups (p = 0.05); a lower incidence of infections at diagnosis in the RT category (20.8%) compared to RA (32%) and RN (43%) categories (p = 0.03); and a higher incidence of hemorrhagic symptoms at diagnosis in the RT category (41.6%) and RN category (26%) as compared to the RA group (5%) (p = 0.001). Application of different scoring systems (Bournemouth and Spanish scores, WPSS) revealed a low OS in high-risk patients within the RT category, compared to RA and RN categories, although unlikely to reflect the consequences of low OS found in the former category. Statistically significant differences were also evidenced in the incidence of acute myeloid leukemia (AML) evolution and overall survival: 7/79 (8%) patients with the RA category evolved to AML in a median time of 89 months, whereas 4/23 (17%) of the RN category and 1/24 (4%) of the RT category experienced disease progression, in a median time of 33.8 and 12.8 months, respectively (p = 0.03). The RT category had a lower overall survival (15.9 months) as compared to RA (48.2 months) and RN (35.9 months) categories (p < 0.001). In conclusion, in our study, application of the revised 2008 WHO classification confirmed the importance of separating patients with unilineage dysplasia for prognostic disease assessment; from our results it seems that the RT category has a worse outcome.
机译:根据经修订的2008年WHO分类,一种骨髓谱系和一种血细胞减少症的≥10%或= 10%的异型增生构成了单谱系血细胞减少和单谱系异型增生(UCUD)的低风险类别。根据WHO的资料,我们从数据库中对低危MDS进行了回顾性重分类,并在诊断时发现了具有这些特征的126名受试者:79例患者归为难治性贫血(RA),23例患者归为难治性中性粒细胞减少症(RN),24例归为难治性血小板减少症(RT)。在性别,中位年龄和细胞遗传畸变方面,我们没有发现这三个亚组之间的差异。在RN类别中观察到较低的PMN计数(0.8 x 10(9)/ L),在RT类别中观察到较低的血小板计数(51 x 10(9)/ L)。此外,与RA(62%)和RN(69%)组相比,RT组(45.8%)的患者在疾病过程中需要RBC输血的比例更低(p = 0.05);与RA(32%)和RN(43%)类别相比,RT类别(20.8%)诊断时的感染发生率较低(p = 0.03);与RA组(5%)相比,RT类(41.6%)和RN类(26%)的诊断时出血症状的发生率更高(p = 0.001)。应用不同的评分系统(伯恩茅斯和西班牙评分,WPSS)显示,与RA和RN类别相比,RT类别的高危患者的OS较低,尽管不太可能反映前者的OS较低的后果。急性髓细胞性白血病(AML)发生率和总生存率方面也有统计学上的显着差异:RA类患者中有7/79(8%)患者在中位时间为89个月内发展为AML,而4/23(17 RN类别的%)和RT类别的1/24(4%)经历了疾病进展,中位时间分别为33.8和12.8个月(p = 0.03)。与RA(48.2个月)和RN(35.9个月)相比,RT类别的总生存期(15.9个月)较低(p <0.001)。总而言之,在我们的研究中,应用经修订的2008 WHO分类标准证实了分离单线型发育异常患者对于评估预后疾病的重要性。从我们的结果来看,RT类别的结果似乎更差。

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