Evidence map›Paper›PMID 32321465›Full record

ArticleBMC cancer2020

Plasmacytoma in patients with multiple myeloma: morphology and immunohistochemistry.

Maiia V Firsova, Larisa P Mendeleeva, Alla M Kovrigina, Maxim V Solovev, Valery G Savchenko

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  7. Article
  8. Review
  9. A Case of Extramedullary Plasmacytoma in Both Maxillary Sinuses.Journal of rhinology : official journal of the Korean Rhinologic Society · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. The Cancer-Immunity Cycle in Multiple Myeloma.ImmunoTargets and therapy · 2021
    Review
  14. Article
  15. 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

5 authors at 1 institution in 1 country.

Maiia V FirsovaDepartment of High-Dose Chemotherapy of Paraproteinemic Hemoblastoses, FSFI «National Research Center for Hematology», 4a Novyi Zykovskii pr, Moscow, Russian Federation, 125167. firs-maia@yandex.ru.
Larisa P MendeleevaDepartment of High-Dose Chemotherapy of Paraproteinemic Hemoblastoses, FSFI «National Research Center for Hematology», 4a Novyi Zykovskii pr, Moscow, Russian Federation, 125167.
Alla M KovriginaDepartment of Pathology, FSFI «National Research Center for Hematology», Moscow, Russian Federation.
Maxim V SolovevDepartment of High-Dose Chemotherapy of Paraproteinemic Hemoblastoses, FSFI «National Research Center for Hematology», 4a Novyi Zykovskii pr, Moscow, Russian Federation, 125167.
Valery G SavchenkoFSFI «National Research Center for Hematology», Moscow, Russian Federation.
Federal State Institution Hematology Research Center · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo study the histological structure and immunohistochemical (IHC) parameters of the plasmacytoma tumour substrate in patients with multiple myeloma (MM).

methodsThe study included 21 patients (10 men/11 women) aged 23 to 73 years old with newly diagnosed MM complicated by plasmacytoma. Bone plasmacytoma was diagnosed in 14 patients, and extramedullary plasmacytoma was diagnosed in 7 patients. Plasmacytoma tissue specimens were examined using a LEICA DM4000B microscope. Anti-CD56, anti-CD166, anti-CXCR4, anti-Ki-67, and anti-c-MYC antibodies were used for IHC study of plasmacytoma biopsies.

resultsWhen comparing the morphology of bone and extramedullary plasmacytoma, no significant differences were revealed; however, the substrate of extramedullary plasmacytoma was more often represented by tumour cells with an immature morphology than was the bone plasmacytoma substrate (57.1% vs. 28.6%, respectively). We revealed a significant difference in the expression of CD166 between bone and extramedullary plasmacytoma. The mean values ​​of CD166 expression in bone plasmacytoma cells were significantly higher (36.29 ± 7.61% versus 9.57 ± 8.46%, respectively; p = 0.033) than those in extramedullary plasmacytoma cells. We noticed that in extramedullary plasmacytoma cells, there were higher values for the Ki-67 index than in bone plasmacytoma cells, and this result was independent of cell morphology.

conclusionThe mechanisms involved in the dissemination of tumour plasma cells are currently unexplored. Even in such a small sample, some differences in expression could be identified, which may indicate that different mechanisms lead to the formation of bone and extramedullary plasmacytomas. Specifically, the expression of CD166 in extramedullary plasmacytoma cells was almost 4 times lower than that in bone plasmacytoma cells, which may indicate the involvement of CD166 in the mechanisms of bone destruction. The proliferative activity of extramedullary plasmacytoma cells was shown to be higher than that of bone plasmacytoma cells.

Indexed as

AdultAgedFemaleFollow-Up StudiesHumansImmunohistochemistryMaleMiddle AgedMultiple MyelomaPlasmacytomaPrognosisYoung AdultCD 166CD56C-MYCCXCR4Extramedullary diseaseImmunohistochemistryKi-67Multiple myelomaPlasmacytoma

Identifiers

PMID32321465
PMCPMC7178964
OpenAlexW3017564201

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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.