Danzero Alice Costanza, Gottardi Enrico Marco, Quarantelli Fabrizio, Del Prete Ciro, Potenza Alessandra, Venturi Claudia, Berchialla Paola, Guerrini Francesca, Bono Clara, Ottaviani Emanuela, Galimberti Sara, Fava Carmen, Izzo Barbara
Department of Clinical and Biological Sciences, Turin University, 10043 Orbassano, Italy.
Oncologic Hematology and Cytogenetics Laboratory, CEINGE Advanced Biotechnology "Franco Salvatore", 80131 Naples, Italy.
Int J Mol Sci. 2025 Sep 13;26(18):8932. doi: 10.3390/ijms26188932.
Chronic myeloid leukemia (CML) is a clonal myeloproliferative disorder caused by the fusion gene, resulting from a reciprocal translocation between chromosomes 22 and 9. Quantification of transcript levels in peripheral blood by RT-qPCR represents the gold standard for molecular response (MR) monitoring, providing essential clinical information on treatment efficacy. Xpert BCR-ABL Ultra is a fully automated in vitro diagnostic test that quantitatively detects e13a2 and e14a2 transcripts using a single-use cartridge that integrates RNA extraction, cDNA synthesis, nested real-time PCR, and signal detection within a rapid, closed, and user-friendly system. In this study, we evaluated Xpert BCR-ABL Ultra as an alternative to validated systems currently used by four highly specialized Italian laboratories affiliated with the Italian national laboratory network for CML. A total of 129 peripheral blood samples from CML patients at various disease stages, along with two external quality control materials, were analyzed. We assessed the test's repeatability, specificity, and stability. Concordance of %IS values generated by the different methods was evaluated using EUTOS criteria and Bland-Altman analysis. Finally, MR value concordance was analyzed based on European LeukemiaNet recommendations or calculated using the formula 2 - log(%IS). Xpert BCR-ABL Ultra demonstrated high repeatability and stability. The %IS values obtained with this assay showed strong concordance with those generated by local reference methods, and MR classifications were consistent across platforms. These findings confirm the robustness, accuracy, and efficiency of the Xpert BCR-ABL Ultra assay, supporting its use as a reliable alternative to currently validated systems for the routine clinical monitoring of CML patients.
慢性粒细胞白血病(CML)是一种由融合基因引起的克隆性骨髓增殖性疾病,该融合基因由22号和9号染色体之间的相互易位产生。通过逆转录定量聚合酶链反应(RT-qPCR)对外周血中的转录水平进行定量分析是分子反应(MR)监测的金标准,可为治疗效果提供重要的临床信息。Xpert BCR-ABL Ultra是一种全自动体外诊断测试,它使用一次性试剂盒定量检测e13a2和e14a2转录本,该试剂盒在一个快速、封闭且用户友好的系统中集成了RNA提取、cDNA合成、巢式实时PCR和信号检测功能。在本研究中,我们评估了Xpert BCR-ABL Ultra作为意大利国家实验室网络下属的四个高度专业化意大利实验室目前使用的经过验证的系统的替代方案。共分析了129份来自处于不同疾病阶段的CML患者的外周血样本以及两种外部质量控制材料。我们评估了该测试的重复性、特异性和稳定性。使用EUTOS标准和布兰德-奥特曼分析评估不同方法产生的%IS值的一致性。最后,根据欧洲白血病网的建议分析MR值的一致性,或使用公式2 - log(%IS)进行计算。Xpert BCR-ABL Ultra显示出高重复性和稳定性。该检测方法获得的%IS值与当地参考方法产生的值高度一致,并且各平台之间的MR分类一致。这些发现证实了Xpert BCR-ABL Ultra检测方法的稳健性、准确性和效率,支持将其用作目前经过验证的系统的可靠替代方案,用于CML患者的常规临床监测。