Rapid and Reproducible Karyotyping with Long Read Sequencing in AML Patients

Acute myeloid leukemia (AML) is characterized by recurrent chromosomal abnormalities that form the basis of the European LeukemiaNet (ELN) risk classification and serve as essential determinants of prognosis and therapeutic decision-making. Conventional metaphase karyotyping remains the diagnostic gold standard for detecting these abnormalities; however, its utility is limited by longer turnaround times, often delaying critical clinical management. Here, we present a long-read sequencing-based (LRS) low-coverage whole genome sequencing (lcWGS) approach using Oxford Nanopore Technology as a rapid and scalable alternative for cytogenetic profiling. A total of 100 diagnostic AML samples were analyzed, comprising 50 retrospectively selected cases with known adverse-risk cytogenetics and 50 prospectively enrolled patients with clinically defined de novo AML. LcWGS demonstrated robust analytical performance, identifying chromosomal aberrations with 93% sensitivity, specificity, and overall accuracy, respectively. Complex karyotypes were reliably detected, with an area under the curve (AUC) of 0.971. Reproducibility was validated through replicate sequencing at two independent laboratories (R=0.99). LcWGS-derived estimates of clone size showed moderate correlation with conventional cytogenetic assessments (R=0.54). Patients with complex karyotypes identified by lcWGS exhibited significantly shorter overall and relapse-free survival, closely mirroring outcomes defined by conventional karyotyping and underscoring the value of lcWGS for risk stratification. Median turnaround time from sample receipt to bioinformatics interpretation was approximately 34 hours, enabling delivery of actionable karyotype results within 72 hours. These findings establish lcWGS as a rapid, reproducible, and accurate platform for detecting clinically relevant chromosomal abnormalities, addressing a critical need for timely risk stratification and treatment initiation in AML.

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Journal
Blood Advances
Published
2026-06-25
DOI
https://doi.org/10.1182/bloodadvances.2026019960
Primary Topic
Acute Myeloid Leukemia Research
Type
article
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article

Rapid and Reproducible Karyotyping with Long Read Sequencing in AML Patients

Arnold Ganser, Mustafa Salim, Anna Dolnik, Frédérik Damm et al.
Blood Advances
Acute Myeloid Leukemia Research
article

Rapid and Reproducible Karyotyping with Long Read Sequencing in AML Patients

Arnold Ganser, Mustafa Salim, Anna Dolnik, Frédérik Damm, Michael Heuser, Konstanze Döhner, Felicitas Thol, Lars Bullinger, Gudrun Göhring, Razif Gabdoulline, Yasmine Alwie, Hartmut Döhner, Isabell Arnhardt, Nikolaus Jahn, Jörg Westermann, Arnold Kloos, Courteney K. Lai, Martin Neugebohren, Yvonne Behrens, Gesa Baurmann, Jens-Florian F Schrezenmeier, Jan Eric Sträng, Doris Steinemann, Jonathan L. Lühmann, Olga Blau
article en

Abstract

Acute myeloid leukemia (AML) is characterized by recurrent chromosomal abnormalities that form the basis of the European LeukemiaNet (ELN) risk classification and serve as essential determinants of prognosis and therapeutic decision-making. Conventional metaphase karyotyping remains the diagnostic gold standard for detecting these abnormalities; however, its utility is limited by longer turnaround times, often delaying critical clinical management. Here, we present a long-read sequencing-based (LRS) low-coverage whole genome sequencing (lcWGS) approach using Oxford Nanopore Technology as a rapid and scalable alternative for cytogenetic profiling. A total of 100 diagnostic AML samples were analyzed, comprising 50 retrospectively selected cases with known adverse-risk cytogenetics and 50 prospectively enrolled patients with clinically defined de novo AML. LcWGS demonstrated robust analytical performance, identifying chromosomal aberrations with 93% sensitivity, specificity, and overall accuracy, respectively. Complex karyotypes were reliably detected, with an area under the curve (AUC) of 0.971. Reproducibility was validated through replicate sequencing at two independent laboratories (R=0.99). LcWGS-derived estimates of clone size showed moderate correlation with conventional cytogenetic assessments (R=0.54). Patients with complex karyotypes identified by lcWGS exhibited significantly shorter overall and relapse-free survival, closely mirroring outcomes defined by conventional karyotyping and underscoring the value of lcWGS for risk stratification. Median turnaround time from sample receipt to bioinformatics interpretation was approximately 34 hours, enabling delivery of actionable karyotype results within 72 hours. These findings establish lcWGS as a rapid, reproducible, and accurate platform for detecting clinically relevant chromosomal abnormalities, addressing a critical need for timely risk stratification and treatment initiation in AML.

Blood Advances
Carl von Ossietzky Universität Oldenburg (DE), Medizinische Hochschule Hannover (DE), Berlin Institute of Health at Charité - Universitätsmedizin Berlin (DE), Amedes Genetics (Germany) (DE), University Hospital Ulm (DE), Martin Luther University Halle-Wittenberg (DE), Charité - Universitätsmedizin Berlin (DE)
Peace, Justice and strong institutions
Openalex Percentile: Top 7%
Acute Myeloid Leukemia Research
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