Evidence map›Paper›PMID 30026572›Full record

ArticleLeukemia2019

Heterogeneous expression of cytokines accounts for clinical diversity and refines prognostication in CMML.

Sandrine Niyongere, Nolwenn Lucas, Jun-Min Zhou, Samer Sansil, Anthony D Pomicter, Maria E Balasis, John Robinson, Jodi Kroeger, Qing Zhang, Yu Long Zhao and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Leukemia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 4% of its field
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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Integrated Human and Murine Clinical Study Establishes Clinical Efficacy of Ruxolitinib in Chronic Myelomonocytic Leukemia.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Trial
  5. Article
  6. The Role of Inflammation in CMML Pathobiology and Progression.Current hematologic malignancy reports · 2025
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
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

18 authors at 4 institutions in 3 countries.

Sandrine NiyongereDepartment of Malignant Hematology, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Nolwenn LucasINSERM U1170, Gustave Roussy Cancer Center, Villejuif, France.
Jun-Min ZhouDepartment of Biostatistics and Bioinformatics, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Samer SansilFlow Cytometry Core, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Anthony D PomicterHuntsman Cancer Institute, The University of Utah, Salt Lake City, UT, USA.
Maria E BalasisDepartment of Malignant Hematology, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.ORCID http://orcid.org/0000-0003-1664-3222
John RobinsonFlow Cytometry Core, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Jodi KroegerFlow Cytometry Core, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Qing ZhangDepartment of Malignant Hematology, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Yu Long ZhaoDepartment of Malignant Hematology, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Markus BallDepartment of Malignant Hematology, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Rami KomrokjiDepartment of Malignant Hematology, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Alan ListDepartment of Malignant Hematology, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Michael W DeiningerHuntsman Cancer Institute, The University of Utah, Salt Lake City, UT, USA.
Brooke L FridleyDepartment of Biostatistics and Bioinformatics, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Valeria SantiniHematology, AOU Careggi, University of Florence, Florence, Italy.
Eric SolaryINSERM U1170, Gustave Roussy Cancer Center, Villejuif, France.
Eric PadronDepartment of Malignant Hematology, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA. Eric.padron@moffitt.org.
Moffitt Cancer Center · USInserm · FRUniversity of Utah · USUniversity of Florence · IT

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
NCI NIH HHS P30 CA076292
6 · The paper itself

Abstract

Chronic myelomonocytic leukemia (CMML) is a clinically heterogeneous neoplasm in which JAK2 inhibition has demonstrated reductions in inflammatory cytokines and promising clinical activity. We hypothesize that annotation of inflammatory cytokines may uncover mutation-independent cytokine subsets associated with novel CMML prognostic features. A Luminex cytokine profiling assay was utilized to profile cryopreserved peripheral blood plasma from 215 CMML cases from three academic centers, along with center-specific, age-matched plasma controls. Significant differences were observed between CMML patients and healthy controls in 23 out of 45 cytokines including increased cytokine levels in IL-8, IP-10, IL-1RA, TNF-α, IL-6, MCP-1/CCL2, hepatocyte growth factor (HGF), M-CSF, VEGF, IL-4, and IL-2RA. Cytokine associations were identified with clinical and genetic features, and Euclidian cluster analysis identified three distinct cluster groups associated with important clinical and genetic features in CMML. CMML patients with decreased IL-10 expression had a poor overall survival when compared to CMML patients with elevated expression of IL-10 (P = 0.017), even when adjusted for ASXL1 mutation and other prognostic features. Incorporating IL-10 with the Mayo Molecular Model statistically improved the prognostic ability of the model. These established cytokines, such as IL-10, as prognostically relevant and represent the first comprehensive study exploring the clinical implications of the CMML inflammatory state.

Indexed as

MutationAdultAgedAged, 80 and overBiomarkers, TumorCase-Control StudiesCytokinesFemaleFollow-Up StudiesHumansInflammation MediatorsLeukemia, Myelomonocytic, ChronicMaleMiddle AgedPrognosisSurvival RateBiomarkers, TumorCytokinesInflammation Mediators

Identifiers

PMID30026572
PMCPMC7787307
OpenAlexW2883082490

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.