Evidence map›Paper›PMID 35709473›Full record

ArticleBlood advances2022

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

Xavier Calvo, David Roman-Bravo, Nieves Garcia-Gisbert, Juan Jose Rodriguez-Sevilla, Sara Garcia-Avila, Lourdes Florensa, Joan Gibert, Concepción Fernández-Rodríguez, Marta Salido, Anna Puiggros and 5 more

Abstract read
In one paragraph

Article in Blood advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Clinical management of CMML-State of the art.British journal of haematology · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Xavier CalvoLaboratori de Citologia Hematològica, Servei de Patologia, Grup de Recerca Translacional en Neoplàsies Hematològiques (GRETNHE), Hospital del Mar Research Institute (IMIM), Barcelona, Spain.ORCID 0000-0001-7934-9130
David Roman-BravoLaboratori de Citologia Hematològica, Servei de Patologia, Grup de Recerca Translacional en Neoplàsies Hematològiques (GRETNHE), Hospital del Mar Research Institute (IMIM), Barcelona, Spain.
Nieves Garcia-GisbertLaboratori de Biologia Molecular, Servei de Patologia, Grup de Recerca Clínica Aplicada en Neoplàsies Hematològiques, IMIM, Barcelona, Spain.ORCID 0000-0002-8185-9786
Juan Jose Rodriguez-SevillaLaboratori de Citologia Hematològica, Servei de Patologia, Grup de Recerca Translacional en Neoplàsies Hematològiques (GRETNHE), Hospital del Mar Research Institute (IMIM), Barcelona, Spain.ORCID 0000-0002-4741-7925
Sara Garcia-AvilaServei d'Hematologia Clínica, Grup de Recerca Clínica Aplicada en Neoplàsies Hematològiques, IMIM, Barcelona, Spain.
Lourdes FlorensaLaboratori de Citologia Hematològica, Servei de Patologia, Grup de Recerca Translacional en Neoplàsies Hematològiques (GRETNHE), Hospital del Mar Research Institute (IMIM), Barcelona, Spain.
Joan GibertLaboratori de Biologia Molecular, Servei de Patologia, Grup de Recerca Clínica Aplicada en Neoplàsies Hematològiques, IMIM, Barcelona, Spain.ORCID 0000-0002-0742-0759
Concepción Fernández-RodríguezLaboratori de Biologia Molecular, Servei de Patologia, Grup de Recerca Clínica Aplicada en Neoplàsies Hematològiques, IMIM, Barcelona, Spain.
Marta SalidoLaboratori de Genètica Molecular, Servei de Patologia, GRETNHE, IMIM, Barcelona, Spain; and.ORCID 0000-0001-9988-5977
Anna PuiggrosLaboratori de Genètica Molecular, Servei de Patologia, GRETNHE, IMIM, Barcelona, Spain; and.ORCID 0000-0001-9627-4978
Blanca EspinetLaboratori de Genètica Molecular, Servei de Patologia, GRETNHE, IMIM, Barcelona, Spain; and.ORCID 0000-0002-4294-8145
Luis ColomoUniversitat Pompeu Fabra, Barcelona, Spain.ORCID 0000-0001-5236-5085
Beatriz BellosilloLaboratori de Biologia Molecular, Servei de Patologia, Grup de Recerca Clínica Aplicada en Neoplàsies Hematològiques, IMIM, Barcelona, Spain.ORCID 0000-0002-5335-2726
Ana FerrerLaboratori de Citologia Hematològica, Servei de Patologia, Grup de Recerca Translacional en Neoplàsies Hematològiques (GRETNHE), Hospital del Mar Research Institute (IMIM), Barcelona, Spain.ORCID 0000-0002-3381-9472
Leonor ArenillasLaboratori de Citologia Hematològica, Servei de Patologia, Grup de Recerca Translacional en Neoplàsies Hematològiques (GRETNHE), Hospital del Mar Research Institute (IMIM), Barcelona, Spain.ORCID 0000-0002-8176-7179

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Leukemia, Myeloid, AcuteLeukemia, Myelomonocytic, ChronicMyelodysplastic SyndromesHumansMutationPrognosis

Identifiers

PMID35709473
PMCPMC9278296

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.