Evidence map›Paper›PMID 25295254›Full record

ReviewBioMed research international2014

New insights into monoclonal B-cell lymphocytosis.

Christina Kalpadakis, Gerassimos A Pangalis, Sotirios Sachanas, Theodoros P Vassilakopoulos, Stavroula Kyriakaki, Penelope Korkolopoulou, Efstathios Koulieris, Maria Moschogiannis, Xanthi Yiakoumis, Pantelis Tsirkinidis and 5 more

Open access · hybridAbstract readReview
In one paragraph

Review in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-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

9 citing papers in PubMed, 19 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

15 authors at 5 institutions in 1 country.

Christina KalpadakisDepartment of Haematology, University Hospital, University of Crete, P.O. BOX 1352, 71110 Heraklion, Crete, Greece.
Gerassimos A PangalisDepartment of Haematology, Athens Medical Center-Psychikon Branch, 11525 Athens, Greece.
Sotirios SachanasDepartment of Haematology, Athens Medical Center-Psychikon Branch, 11525 Athens, Greece.
Theodoros P VassilakopoulosDepartment of Haematology, University of Athens, Laikon General Hospital, 11527 Athens, Greece.
Stavroula KyriakakiDepartment of Haematology, University Hospital, University of Crete, P.O. BOX 1352, 71110 Heraklion, Crete, Greece.
Penelope KorkolopoulouDepartment of Pathology, University of Athens, 11527 Athens, Greece.
Efstathios KoulierisDepartment of Haematology, Athens Medical Center-Psychikon Branch, 11525 Athens, Greece.
Maria MoschogiannisDepartment of Haematology, Athens Medical Center-Psychikon Branch, 11525 Athens, Greece.
Xanthi YiakoumisDepartment of Haematology, Athens Medical Center-Psychikon Branch, 11525 Athens, Greece.
Pantelis TsirkinidisDepartment of Haematology, Athens Medical Center-Psychikon Branch, 11525 Athens, Greece ; Department of Haematology, 401 Military Hospital, 11525 Athens, Greece.
Marie-Christine Kyrtsonis1st Department of Propedeutics, University of Athens, Laikon General Hospital, 11527 Athens, Greece.
Georgia LevidouDepartment of Pathology, University of Athens, 11527 Athens, Greece.
Helen A PapadakiDepartment of Haematology, University Hospital, University of Crete, P.O. BOX 1352, 71110 Heraklion, Crete, Greece.
Panayiotis Panayiotidis1st Department of Propedeutics, University of Athens, Laikon General Hospital, 11527 Athens, Greece.
Maria K AngelopoulouDepartment of Haematology, University of Athens, Laikon General Hospital, 11527 Athens, Greece.
Athens Medical Center · GRNational and Kapodistrian University of Athens · GRUniversity of Crete · GRUniversity General Hospital Attikon · GR401 General Military Hospital of Athens · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monoclonal B-cell lymphocytosis (MBL) is a premalignant condition characterized by the presence of less than 5000/μL circulating clonal B cells in otherwise healthy individuals. Three subcategories have been identified according to the immunophenotypic features: CLL-like, CD5(+) atypical, and CD5(-) MBL. CLL-like MBL is by far the most frequent and best studied category and further divided in low-count [LC] and high-count [HC] MBL, based on a cutoff value of 500/μL clonal B cells. LC-MBL typically remains stable and probably does not represent a truly premalignant condition, but rather an age-related immune senescence. On the other hand, HC-MBL is closely related to CLL-Rai0, bearing similar immunogenetic profile, and is associated with an annual risk of progression to CLL requiring therapy at a rate of 1.1%. Currently there are no reproducible factors for evaluating the risk of progression to CLL. CD5(-) MBL is characterized by an immunophenotype consistent with marginal zone origin and displays many similarities with marginal zone lymphomas (MZL), mainly the splenic MZL. The cutoff value of 5000/μL clonal B cells cannot probably be applied in CD5(-) MBL, requiring a new definition to describe those cases.

Indexed as

AdultB-LymphocytesCD5 AntigensHumansImmunophenotypingLeukemia, Lymphocytic, Chronic, B-CellLymphocyte CountLymphocytosisCD5 Antigens

Identifiers

PMID25295254
PMCPMC4177785
OpenAlexW1968485411

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.