4.7 Article

Minimal residual disease in BCR::ABL1-positive acute lymphoblastic leukemia: different significance in typical ALL and in CML-like disease

Journal

LEUKEMIA
Volume -, Issue -, Pages -

Publisher

SPRINGERNATURE
DOI: 10.1038/s41375-022-01668-0

Keywords

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Funding

  1. Czech Health Research Council [NU2103-00128]
  2. Charles University [UNCE 204012]
  3. Ministry of Health, Czech Republic
  4. University Hospital Motol, Prague, Czech Republic [00064203]
  5. project National Institute for Cancer Research (Program EXCELES) - European Union-Next Generation EU [LX22NPO5102]
  6. Deutsche Krebshilfe [70112958]
  7. Italian Association for Cancer Research (AIRC) [IG2017-20564, IG2015-17593]
  8. Comitato Maria Letizia Verga

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In this retrospective analysis, the prognostic relevance of minimal residual disease (MRD) and other features in BCR::ABL1-positive ALL were investigated. The study found that BCR::ABL1-positive ALL can be divided into typical ALL and CML-like subtype. The overall prognosis of typical ALL and CML-like patients was similar, but there were differences in relapse rates and mortality. MRD had a significant prognostic role in typical ALL, while it was not significant in CML-like patients. The study suggests that early distinguishing between typical BCR::ABL1-positive ALL and CML-like patients is important for optimal treatment approaches.
Recently, we defined CML-like subtype of BCR::ABL1-positive acute lymphoblastic leukemia (ALL), resembling lymphoid blast crisis of chronic myeloid leukemia (CML). Here we retrospectively analyzed prognostic relevance of minimal residual disease (MRD) and other features in 147 children with BCR::ABL1-positive ALL (diagnosed I/2000-IV/2021, treated according to EsPhALL (n = 133) or other (n = 14) protocols), using DNA-based monitoring of BCR::ABL1 genomic breakpoint and clonal immunoglobulin/T-cell receptor gene rearrangements. Although overall prognosis of CML-like (n = 48) and typical ALL (n = 99) was similar (5-year-EFS 60% and 49%, respectively; 5-year-OS 75% and 73%, respectively), typical ALL presented more relapses while CML-like patients more often died in the first remission. Prognostic role of MRD was significant in the typical ALL (p = 0.0005 in multivariate analysis for EFS). In contrast, in CML-like patients MRD was not significant (p values > 0.2) and inapplicable for therapy adjustment. Moreover, in the typical ALL, risk-prediction could be further improved by considering initial hyperleukocytosis. Early distinguishing typical BCR::ABL1-positive ALL and CML-like patients is essential to enable optimal treatment approach in upcoming protocols. For the typical ALL, tyrosine-kinase inhibitors and concurrent chemotherapy with risk-directed intensity should be recommended; in the CML-like disease, no relevant prognostic feature applicable for therapy tailoring was found so far.

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