Feasible and Rapid Screening of <i>IDH1/2</i> and <i>FLT3-TKD2</i> Mutations by High-Resolution Melting for Patients with Acute Myeloid Leukemia

Feasible and Rapid Screening of <i>IDH1/2</i> and <i>FLT3-TKD2</i> Mutations by High-Resolution Melting for Patients with Acute Myeloid Leukemia

<b>Background</b>: In recent years, numerous recurrently mutated genes have been identified in acute myeloid leukemia (AML), some of which, such as <i>FLT3</i> and <i>IDH1/2</i>, serve as therapeutic targets, offering new treatment options. Rapid mutational analys...

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Main Authors: José Vicente Gil, Sandra de las Heras, Alberto Miralles, Claudia Sargas, Marta Llop, Rebeca Rodríguez-Veiga, Laura Torres-Miñana, Blanca Boluda, Isabel Cano-Ferri, Evelyn Acuña-Cruz, Irene Navarro, Pilar Lloret-Madrid, Pau Montesinos, Eva Barragán
Format: Article
Language:English
Published: MDPI AG 2025-05-01
Series:Diagnostics
Subjects:
acute myeloid leukemia (AML)
high resolution melting (HRM)
targeted therapies
<i>IDH1/2</i>
<i>FLT3-TKD2</i>
mutation screening
Online Access:https://www.mdpi.com/2075-4418/15/10/1230
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Summary:<b>Background</b>: In recent years, numerous recurrently mutated genes have been identified in acute myeloid leukemia (AML), some of which, such as <i>FLT3</i> and <i>IDH1/2</i>, serve as therapeutic targets, offering new treatment options. Rapid mutational analysis is crucial for timely and optimal therapy selection. This study aims to develop and validate a rapid, cost-effective, and sensitive screening method for detecting <i>IDH1</i>, <i>IDH2</i>, and <i>FLT3</i>-TKD2 mutations using polymerase chain reaction (PCR) and high-resolution melting curve analysis (HRM). <b>Methods</b>: A PCR-HRM assay was developed to simultaneously detect mutations in <i>IDH1</i>, <i>IDH2</i>, and <i>FLT3</i>-TKD2. The method was applied to a cohort of 1363 AML patients, and its performance, including turnaround time, was evaluated through comparison with next-generation sequencing (NGS) results. <b>Results</b>: The PCR-HRM method demonstrated a positive percent agreement of 98%, 98%, and 92% for <i>IDH1</i>, <i>IDH2</i>, and <i>FLT3-TKD2</i>, respectively, and a negative percent agreement of 100% for all three genes compared to NGS. No false positives were observed, and false negatives were detected in less than 1% of cases, mostly in <i>FLT3</i>-TKD2, all occurring below the established limit of detection. The turnaround time and cost of PCR-HRM were significantly lower than those of NGS. <b>Conclusions</b>: This method offers a highly sensitive, specific, and time-efficient approach for the simultaneous detection of <i>IDH1</i>, <i>IDH2</i>, and <i>FLT3</i>-TKD2 mutations in AML patients. Its rapid turnaround time and cost-effectiveness make it a valuable tool for routine clinical screening, facilitating timely and targeted treatment decisions.
ISSN:2075-4418

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