Evidence map›Paper›PMID 37316755›Full record

ArticleMedical oncology (Northwood, London, England)2023

Circulating cancer giant cells with unique characteristics frequently found in patients with myelodysplastic syndromes (MDS).

Abdullah Mahmood Ali, Fatima BenMohamed, Alessandra Decina, Sanjay Mukherjee, Shelley Levi, Laura Nalleli Garrido Castillo, Davide Bréchot, Joseph Jurcic, Azra Raza, Patrizia Paterlini Bréchot

Open access · hybridAbstract read
In one paragraph

Article in Medical oncology (Northwood, London, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

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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

10 authors at 3 institutions in 3 countries.

Abdullah Mahmood Ali *Division of Hematology/Oncology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Fatima BenMohamed *Rarecells Diagnostics, Faculté de Médecine Necker, 160 rue de Vaugirard, 75015, Paris, France.
Alessandra DecinaRarecells Diagnostics, Faculté de Médecine Necker, 160 rue de Vaugirard, 75015, Paris, France.
Sanjay MukherjeeDivision of Hematology/Oncology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Shelley LeviDivision of Hematology/Oncology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Laura Nalleli Garrido CastilloRarecells Diagnostics, Faculté de Médecine Necker, 160 rue de Vaugirard, 75015, Paris, France.
Davide BréchotRarecells Diagnostics, Faculté de Médecine Necker, 160 rue de Vaugirard, 75015, Paris, France.
Joseph JurcicDivision of Hematology/Oncology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA.
Azra Raza *Division of Hematology/Oncology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, 10032, USA. azra.raza@columbia.edu.ORCID http://orcid.org/0000-0002-9734-5210
Patrizia Paterlini Bréchot *Rarecells Diagnostics, Faculté de Médecine Necker, 160 rue de Vaugirard, 75015, Paris, France. patrizia.paterlini@rarecells.com.ORCID http://orcid.org/0000-0001-7981-6325
Columbia University Irving Medical Center · USDélégation Paris 7 · FRLaunchpad Central (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myelodysplastic syndromes (MDS) are incurable diseases characterized by dysplastic hematopoietic cells, cytopenias in the blood and an inherent tendency for transformation to secondary acute myeloid leukemia (AML). Since most therapies fail to prevent rapid clonal evolution and disease resistance, new and non-invasive predictive markers are needed to monitor patients and adapt the therapeutic strategy. By using ISET, a very sensitive approach to isolate cells larger than mature leukocytes from peripheral blood samples, we looked for cellular markers in 99 patients (158 samples) with MDS and 66 healthy individuals (76 samples) used as controls. We found a total of 680 Giant Cells, defined as cells having a size of 40 microns or larger in 46 MDS patients (80 samples) and 28 Giant Cells in 11 healthy individuals (11 samples). In order to understand if we had enriched from peripheral blood atypical cells of the megakaryocyte line, we studied the Giant Cells using immunolabeling with megakaryocytes and tumor-specific markers. We report that the Giant Cells we found in the peripheral blood of MDS patients primarily express tumor markers. Our results show that Polyploid Giant Cancer Cells (PGCC), similar to those described in solid tumors, are found in the peripheral blood of patients with MDS and suggest the working hypothesis that they could play a role in hematological malignancies.

Indexed as

Hematologic NeoplasmsMyelodysplastic SyndromesNeoplastic Cells, CirculatingBiomarkers, TumorGiant CellsHumansBiomarkers, TumorGiant cellsISETMDSMyelodysplastic syndromesPGCCPolyploid giant cancer cellsTumor markers

Identifiers

PMID37316755
PMCPMC10267270
OpenAlexW4380627988

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Registered trials

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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.