4.6 Article

Outcomes and molecular profile of oligomonocytic CMML support its consideration as the first stage in the CMML continuum

Journal

BLOOD ADVANCES
Volume 6, Issue 13, Pages 3921-3931

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ELSEVIER
DOI: 10.1182/bloodadvances.2022007359

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Funding

  1. ISCI [II-FEDER FIS PI16/0153, FIS PI17/313, FIS PI19/0005, 2017SGR205, 2017SGR437]
  2. Xarxa de Banc de Tumors de Catalunya

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This study aimed to provide survival outcome data of patients with oligomonocytic chronic myelomonocytic leukemia (OM-CMML) and compare them with other types of chronic myelomonocytic leukemia. The results showed that patients with OM-CMML had longer survival and specific gene mutations were identified as adverse prognostic factors. Furthermore, the study demonstrated an evolutionary continuum between OM-CMML, dysplastic CMML, and proliferative CMML.
Patients with oligomonocytic chronic myelomonocytic leukemia (OM-CMML) are currently classified according to the 2017 World Health Organization myelodysplastic syndromes classification. However, recent data support considering OM-CMML as a specific subtype of chronic myelomonocytic leukemia (CMML), given their similar clinical, genomic, and immunophenotypic profiles. The main purpose of our study was to provide survival outcome data of a well-annotated series of 42 patients with OM-CMML and to compare them to 162 patients with CMML, 120 with dysplastic type (D-CMML), and 42 with proliferative type (P-CMML). OM-CMML had significantly longer overall survival (OS) and acute myeloid leukemia-free survival than did patients with CMML, considered as a whole group, and when compared with D-CMML and P-CMML. Moreover, gene mutations associated with increased proliferation (ie, ASXL1 and RAS-pathway mutations) were identified as independent adverse prognostic factors for OS in our series. We found that at a median follow-up of 53.47 months, 29.3% of our patients with OM-CMML progressed to D-CMML, and at a median follow-up of 46.03 months, 28.6% of our D-CMML group progressed to P-CMML. These data support the existence of an evolutionary continuum of OM-CMML, D-CMML, and P-CMML. In this context, we observed that harboring more than 3 mutated genes, carrying ASXL1 mutations, and a peripheral blood monocyte percentage .20% significantly predicted a shorter time of progression of OM-CMML into overt CMML. These variables were also detected as independent adverse prognostic factors for OS in OM-CMML. These data support the consideration of OM-CMML as the first evolutionary stage within the proliferative continuum of CMML.

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