Prognostic Significance of Flow Cytometric Immunophenotyping in Patients with Acute Myeloid Leukemia

IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL Bezmialem Science Pub Date : 2022-08-19 DOI:10.14235/bas.galenos.2021.5875
Sinan Demircioğlu, Ömer Ekinci, Ali Doğan, T. Ulaş
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Abstract

Objective: Chromosomal abnormalities are one of the most important prognostic factors in acute myeloid leukemia (AML). However, not all patients may have such informative chromosomal abnormalities. Although there are many studies on the prognostic value of immunophenotyping in AML, it is still not used as a prognostic marker. In this study, we aimed to investigate the effects of CD13, CD33, CD34, CD117, MPO and HLADR expressions on prognosis of non-acute promyelocytic leukemia AML. Methods: One hundred thirteen patients diagnosed as having non-acute promyelocytic leukemia AML and followed up between 2010 and 2018 were included in this study. The associations of CD13, CD33, CD34, CD117, MPO and HLA DR expressions with chemotherapy response, progression free survival (PFS) and overall survival (OS) were statistically analyzed. Results: It was seen that response to chemotherapy decitabine were evaluated for response after 4-6 cycles. Treatment was continued with responders until progression. Flow cytometric immunophenotyping was performed on bone marrow aspirate. Specimen processing was performed according to a routine red cell lysis protocol. Single cell suspensions were stained with various 4 fluorochrome-conjugated antibody combinations and analyzed in reference to isotype-matched fluorochrome-conjugated control antibodies. Immunophenotypic properties were evaluated with Multiparametric Cytometry MPO expression was shown to be an independent risk factor for PFS and OS in our own patient population.
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流式细胞免疫分型在急性髓系白血病患者中的预后意义
目的:染色体异常是急性粒细胞白血病(AML)最重要的预后因素之一。然而,并不是所有的患者都可能有这样的染色体异常。尽管有许多关于AML免疫表型的预后价值的研究,但它仍然没有被用作预后标志物。本研究旨在探讨CD13、CD33、CD34、CD117、MPO和HLADR表达对非急性早幼粒细胞白血病AML预后的影响。方法:本研究纳入了113名诊断为非急性早幼粒细胞白血病AML并在2010年至2018年间进行随访的患者。统计分析CD13、CD33、CD34、CD117、MPO和HLA DR表达与化疗反应、无进展生存期(PFS)和总生存期(OS)的关系。结果:在4-6个周期后,对地西他滨的化疗反应进行了评估。有反应者继续治疗,直到病情进展。对骨髓吸出物进行流式细胞术免疫表型分析。根据常规红细胞裂解方案进行样品处理。单细胞悬浮液用各种4种荧光染料偶联的抗体组合染色,并参照同种型匹配的荧光染料偶联对照抗体进行分析。免疫表型特性通过多参数细胞测定法进行评估MPO表达在我们自己的患者群体中被证明是PFS和OS的独立风险因素。
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Bezmialem Science
Bezmialem Science MEDICINE, GENERAL & INTERNAL-
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