Minimal residual disease detection for acute lymphoblastic leukaemia in peripheral blood—Are we there yet?

Can peripheral blood be used to detect residual disease in acute lymphoblastic leukaemia (ALL) when we increase the sensitivity of the method used? Bendig et al. found that a larger amount of material and the use of next-generation sequencing (NGS) detects MRD in peripheral blood in up to half of patients with B-cell precursor ALL (BCP-ALL) where routine examination was negative. However, a negative result does not exclude the presence of residual disease and thus still limits the use of peripheral blood. Commentary on: Bendig et al. Next-generation sequencing and high DNA input identify previously missed measurable residual disease in peripheral blood of B-cell precursor acute lymphoblastic leukaemia. Br J Haematol 2025; 206:353-356.

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Publication Details

Journal
British Journal of Haematology
Published
2024-11-11
DOI
https://doi.org/10.1111/bjh.19888
Citations
1
Primary Topic
Acute Lymphoblastic Leukemia research
Type
article
Field-Weighted Citation Impact
0.54
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article

Minimal residual disease detection for acute lymphoblastic leukaemia in peripheral blood—Are we there yet?

Jan Trka, Eva Froňková
1 citations
British Journal of Haematology
Acute Lymphoblastic Leukemia research
0.54
article

Minimal residual disease detection for acute lymphoblastic leukaemia in peripheral blood—Are we there yet?

Jan Trka, Eva Froňková
article en
1 citations

Abstract

Can peripheral blood be used to detect residual disease in acute lymphoblastic leukaemia (ALL) when we increase the sensitivity of the method used? Bendig et al. found that a larger amount of material and the use of next-generation sequencing (NGS) detects MRD in peripheral blood in up to half of patients with B-cell precursor ALL (BCP-ALL) where routine examination was negative. However, a negative result does not exclude the presence of residual disease and thus still limits the use of peripheral blood. Commentary on: Bendig et al. Next-generation sequencing and high DNA input identify previously missed measurable residual disease in peripheral blood of B-cell precursor acute lymphoblastic leukaemia. Br J Haematol 2025; 206:353-356.

British Journal of HaematologyVol. 206(1)
Charles University (CZ)
Openalex Percentile: Top 27%
Acute Lymphoblastic Leukemia research
0.54
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