Department of Hematology and Bone Marrow Transplantation, Poznan University of Medical Sciences, Poznan, Poland.
Department of Hematology, Blood Neoplasms and Bone Marrow Transplantation, Wroclaw Medical University, Wroclaw, Poland.
Scand J Immunol. 2021 Aug;94(2):e13028. doi: 10.1111/sji.13028. Epub 2021 Feb 22.
This analysis attempts to determine the diagnostic and prognostic value of bone marrow (BM) evaluation by multiparameter flow cytometry in patients with myelodysplastic syndrome (MDS).
The study group consisted of patients who underwent diagnostic process in the years 2008-2017 due to cytopenia and finally were diagnosed with MDS (n = 71). The comparative group included patients with cytopenia diagnosed in the same period, whose definitive diagnosis was other than MDS (n = 39). Flow cytometric evaluation of BM was performed following the recommendations of the European LeukemiaNet (ELN) in all patients.
The median number of immunophenotypic abnormalities found on granulocytes in the MDS group was significantly higher compared to the comparative group [2 (range 0-5) vs 0 (range 0-2); P < .0001]. Similarly, the median Ogata score was significantly higher in the MDS group [2 (range 0-4) vs 1 (range 0-3); P < .0001]. Since the disturbances of the CD11b/HLA-DR and CD11b/CD13 on granulocytes were significantly more common in MDS patients, the Ogata score was extended by these abnormalities, what resulted in its higher diagnostic sensitivity (82%) while preserving high specificity (87%). The positive correlation was found between risk score determined by the Revised International Prognostic Scoring System and the number of the BM immunophenotypic abnormalities (P = .017).
Our results indicate that the diagnostic usefulness of the Ogata score may be increased by including the abnormal expression of CD11b/HLA-DR and CD11b/CD13 on granulocytes. Moreover, our findings suggest the prognostic significance of the number of BM cytometric abnormalities in MDS.
本分析试图确定骨髓(BM)多参数流式细胞术评估在骨髓增生异常综合征(MDS)患者中的诊断和预后价值。
研究组包括 2008 年至 2017 年间因血细胞减少症接受诊断过程并最终诊断为 MDS 的患者(n=71)。对照组包括同期诊断为血细胞减少症但最终诊断非 MDS 的患者(n=39)。所有患者均按照欧洲白血病网络(ELN)的建议进行 BM 流式细胞术评估。
MDS 组粒细胞免疫表型异常的中位数明显高于对照组[2(范围 0-5)比 0(范围 0-2);P<0.0001]。同样,MDS 组的中位数 Ogata 评分也明显更高[2(范围 0-4)比 1(范围 0-3);P<0.0001]。由于粒细胞上 CD11b/HLA-DR 和 CD11b/CD13 的异常更为常见,因此 Ogata 评分通过这些异常扩展,从而提高了诊断敏感性(82%),同时保持了高特异性(87%)。修订后的国际预后评分系统确定的风险评分与 BM 免疫表型异常的数量之间存在正相关(P=0.017)。
我们的结果表明,通过包括粒细胞上 CD11b/HLA-DR 和 CD11b/CD13 的异常表达,Ogata 评分的诊断用途可能会增加。此外,我们的发现表明 MDS 中 BM 细胞计数异常的数量具有预后意义。