Evidence map›Paper›PMID 37705525›Full record

ArticleMediterranean journal of hematology and infectious diseases2023

Multiparametric Flow Cytometry in Newly Diagnosed Multiple Myeloma Patients: An Italian Monocentric Experience.

Francesca Fazio, Gianfranco Lapietra, Maria Zaira Limongi, Stefania Intoppa, Maria Laura Milani, Alfonso Piciocchi, Maurizio Martelli, Anna Guarini, Robin Foà, Maria Stefania De Propris and 1 more

Abstract read
In one paragraph

Article in Mediterranean journal of hematology and infectious diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Evaluation of CD56 and CD117 Double-Positivity as a Predictor of Poor Prognosis in Multiple Myeloma Patients: A Retrospective AnalysisTurkish journal of haematology : official journal of Turkish Society of Haematology · 2024
    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

11 authors.

Francesca FazioHematology, Department of Translational and Precision Medicine, Sapienza University, 00161 Rome, Italy.
Gianfranco LapietraHematology, Department of Translational and Precision Medicine, Sapienza University, 00161 Rome, Italy.
Maria Zaira LimongiHematology, Department of Translational and Precision Medicine, Sapienza University, 00161 Rome, Italy.
Stefania IntoppaHematology, Department of Translational and Precision Medicine, Sapienza University, 00161 Rome, Italy.
Maria Laura MilaniHematology, Department of Translational and Precision Medicine, Sapienza University, 00161 Rome, Italy.
Alfonso PiciocchiGruppo Italiano Malattie Ematologiche dell'Adulto (GIMEMA) Data Center, Fondazione GIMEMA Franco Mandelli Onlus.
Maurizio MartelliHematology, Department of Translational and Precision Medicine, Sapienza University, 00161 Rome, Italy.
Anna GuariniDepartment of Molecular Medicine, Sapienza University, Rome, Italy.
Robin FoàHematology, Department of Translational and Precision Medicine, Sapienza University, 00161 Rome, Italy.
Maria Stefania De ProprisHematology, Department of Translational and Precision Medicine, Sapienza University, 00161 Rome, Italy.
Maria Teresa PetrucciHematology, Department of Translational and Precision Medicine, Sapienza University, 00161 Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a heterogeneous malignancy characterized by the proliferation of abnormal plasma cells in the bone marrow. Multiparametric flow cytometry (MFC) plays a role in the work-up of the disease in view of the aberrant expression of surface antigens. Our study aimed at describing the antigenic profile detected by MFC in a series of newly diagnosed MM patients to correlate the level of expression with other features of the disease. Between April 2018 and June 2022, 84 consecutive MM patients were studied at presentation. CD56 and CD117 were commonly detected, while CD45, CD28, CD20, CD19, CD13 and CD33 were less recurrent. CD20 expression was associated with the type of secretory MM (p=0.041) and with a higher disease burden (p=0.038). CD28 positivity correlated with a lower platelet count at baseline (p=0.005) and with a lower rate of complete response (p=0.038). Furthermore, CD28 positivity and a lower CD138 expression tended to associate with the high-risk chromosomal translocations t(14;16) and t(4;14). The results of this study indicate that in the diagnostic work-up of MM, MFC may help to identify different patient subsets and improve risk stratification. These observations need to be validated in larger series of patients with a longer follow-up.

Indexed as

Chromosomal translocationsFluorescence in situ hybridizationKaryotypeMarkersMultiparametric flow cytometryMultiple myeloma

Identifiers

PMID37705525
PMCPMC10497315

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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.