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AML classification in the year 2023: How to avoid a Babylonian confusion of languages. | LitMetric

AI Article Synopsis

  • A new International Consensus Classification (ICC) for hematolymphoid tumors has been introduced alongside the 2022 WHO classification, focusing on more genetics-based definitions for acute myeloid leukemia (AML).
  • An analysis of 717 myelodysplastic syndrome (MDS) and 734 AML patients showed a significant decrease in purely morphologically defined AML entities, while myelodysplasia-related AML classifications increased.
  • Differences in classification criteria, especially regarding TP53 mutated cases, led to variations in overall survival rates, highlighting the need for further studies to clarify ambiguous categorizations.

Article Abstract

In parallel to the 5th edition of the World Health Organization Classification of Haematolymphoid Tumours (WHO 2022), an alternative International Consensus Classification (ICC) has been proposed. To evaluate the impact of the new classifications on AML diagnoses and ELN-based risk classification, we analyzed 717 MDS and 734 AML non-therapy-related patients diagnosed according to the revised 4th WHO edition (WHO 2017) by whole genome and transcriptome sequencing. In both new classifications, the purely morphologically defined AML entities decreased from 13% to 5%. Myelodysplasia-related (MR) AML increased from 22% to 28% (WHO 2022) and 26% (ICC). Other genetically-defined AML remained the largest group, and the abandoned AML-RUNX1 was mainly reclassified as AML-MR (WHO 2022: 77%; ICC: 96%). Different inclusion criteria of AML-CEBPA and AML-MR (i.a. exclusion of TP53 mutated cases according to ICC) were associated with differences in overall survival. In conclusion, both classifications focus on more genetics-based definitions with similar basic concepts and a large degree of agreement. The remaining non-comparability (e.g., TP53 mutated AML) needs additional studies to definitely answer open questions on disease categorization in an unbiased way.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10317829PMC
http://dx.doi.org/10.1038/s41375-023-01909-wDOI Listing

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