Evidence map›Paper›PMID 38194088›Full record

ArticleAnnals of hematology2024

Diagnostic management of blastic plasmacytoid dendritic cell neoplasm (BPDCN) in close interaction with therapeutic considerations.

Evgenii Shumilov, Paolo Mazzeo, Susanne Ghandili, Axel Künstner, Sören Weidemann, Yara Banz, Philipp Ströbel, Matthias Pollak, Lina Kolloch, Helmut Beltraminelli and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Annals of hematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.7field-weighted citation impact, top 8% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Observational
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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

22 authors at 7 institutions in 2 countries.

Evgenii ShumilovDepartment of Medicine A for Hematology, Oncology and Pneumology, University Hospital Muenster, Muenster, Germany.
Paolo MazzeoClinics of Hematology and Medical Oncology, INDIGHO Laboratory, University Medical Center Goettingen (UMG), Goettingen, Germany.
Susanne GhandiliDepartment of Oncology, Hematology and Bone Marrow Transplantation With Section Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Axel KünstnerMedical Systems Biology Group, Luebeck Institute of Experimental Dermatology, University of Luebeck, Luebeck, Germany.
Sören WeidemannInstitute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Yara BanzInstitute of Pathology, University of Bern, Bern, Switzerland.
Philipp StröbelInstitute of Pathology, University Medical Center Goettingen, Goettingen, Germany.
Matthias PollakDepartment of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Lina KollochDepartment of Medicine A for Hematology, Oncology and Pneumology, University Hospital Muenster, Muenster, Germany.
Helmut BeltraminelliDermatopathology Department, Ente Ospedaliero Cantonale (EOC), Locarno, Switzerland.
Andrea KerkhoffDepartment of Medicine A for Hematology, Oncology and Pneumology, University Hospital Muenster, Muenster, Germany.
Jan-Henrik MikeschDepartment of Medicine A for Hematology, Oncology and Pneumology, University Hospital Muenster, Muenster, Germany.
Christoph SchliemannDepartment of Medicine A for Hematology, Oncology and Pneumology, University Hospital Muenster, Muenster, Germany.
Detlef HaaseClinics of Hematology and Medical Oncology, INDIGHO Laboratory, University Medical Center Goettingen (UMG), Goettingen, Germany.
Gerald WulfDepartment of Hematology and Medical Oncology, University Medical Center Goettingen (UMG), Goettingen, Germany.
Myriam LegrosDepartment of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Georg LenzDepartment of Medicine A for Hematology, Oncology and Pneumology, University Hospital Muenster, Muenster, Germany.
Laurence FeldmeyerDepartment of Dermatology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Thomas PabstDepartment of Medical Oncology, Bern University Hospital, University of Bern, InselspitalBern, Switzerland.
Hanno WitteDepartment for Hematology and Oncology, University Hospital Schleswig-Holstein, Campus Luebeck, Luebeck, Germany.
Niklas GebauerDepartment for Hematology and Oncology, University Hospital Schleswig-Holstein, Campus Luebeck, Luebeck, Germany.
Ulrike BacherDepartment of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland. veraulrike.bacher@insel.ch.
University Hospital Münster · DEUniversity of Bern · CHUniversity Medical Center Hamburg-Eppendorf · DEUniversity of Lübeck · DEEnte Ospedaliero Cantonale · CHUniversity Hospital of Bern · CHUniversity Hospital Schleswig-Holstein · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Blastic plasmacytoid dendritic cell neoplasm (BPDCN), a rare malignancy derived from plasmacytoid dendritic cells, can mimic both acute leukemia and aggressive T-cell lymphoma. Therapy of this highly aggressive hematological disease should be initiated as soon as possible, especially in light of novel targeted therapies that have become available. However, differential diagnosis of BPDCN remains challenging. This retrospective study aimed to highlight the challenges to timely diagnoses of BPDCN. We documented the diagnostic and clinical features of 43 BPDCN patients diagnosed at five academic hospitals from 2001-2022. The frequency of BPDCN diagnosis compared to AML was 1:197 cases. The median interval from the first documented clinical manifestation to diagnosis of BPDCN was 3 months. Skin (65%) followed by bone marrow (51%) and blood (45%) involvement represented the most common sites. Immunophenotyping revealed CD4 + , CD45 + , CD56 + , CD123 + , HLA-DR + , and TCL-1 + as the most common surface markers. Overall, 86% (e.g. CD33) and 83% (e.g., CD7) showed co-expression of myeloid and T-cell markers, respectively. In the median, we detected five genomic alterations per case including mutational subtypes typically involved in AML: DNA methylation (70%), signal transduction (46%), splicing factors (38%), chromatin modification (32%), transcription factors (32%), and RAS pathway (30%), respectively. The contribution of patients (30%) proceeding to any form of upfront stem cell transplantation (SCT; autologous or allogeneic) was almost equal resulting in beneficial overall survival rates in those undergoing allogeneic SCT (p = 0.0001). BPDCN is a rare and challenging entity sharing various typical characteristics of other hematological diseases. Comprehensive diagnostics should be initiated timely to ensure appropriate treatment strategies.

Indexed as

Hematologic NeoplasmsLeukemia, Myeloid, AcuteMyeloproliferative DisordersSkin NeoplasmsBone MarrowDendritic CellsHLA-DR AntigensHumansRetrospective StudiesHLA-DR AntigensBlastic plasmacytoid dendritic cell neoplasm (BPDCN)CD123Comprehensive diagnosticsFlow cytometryImmunohistochemistryTagraxofusp

Identifiers

PMID38194088
PMCPMC11009756
OpenAlexW4390727211

What OpenQuestion holds

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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.