Evidence mapPaperPMID 41535617Full record

ArticleAnnals of hematology2026

Sustained response to minimal-dose tagraxofusp in a patient with BPDCN and advanced chronic kidney disease.

Christina Brummer, Katja Evert, Felix Keil, Jakob Schmidt, Matthias Grube, Wolfgang Herr, Markus Radsak, Stephanie Mayer

Abstract readCase Reports
In one paragraph

Article in Annals of hematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
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 synthesis or guideline pooled it.

  1. Pooled it
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

8 authors.

Christina BrummerDepartment of Hematology and Oncology, University Hospital of Regensburg, Regensburg, Germany. christina.brummer@ukr.de.
Katja EvertDepartment of Pathology, University Hospital of Regensburg, Regensburg, Germany.
Felix KeilDepartment of Pathology, University Hospital of Regensburg, Regensburg, Germany.
Jakob SchmidtDepartment of Hematology and Oncology, University Hospital of Regensburg, Regensburg, Germany.
Matthias GrubeDepartment of Hematology and Oncology, University Hospital of Regensburg, Regensburg, Germany.
Wolfgang HerrDepartment of Hematology and Oncology, University Hospital of Regensburg, Regensburg, Germany.
Markus RadsakDepartment of Hematology and Oncology, Hospital of Deggendorf, Deggendorf, Germany.
Stephanie MayerDepartment of Hematology and Oncology, University Hospital of Regensburg, Regensburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is an extremely rare hematologic malignancy with an aggressive course and poor prognosis. Treatment remains challenging particularly in patients who are ineligible for stem cell transplantation due to resistance to conventional chemotherapy. The introduction of tagraxofusp, a CD123-directed cytotoxin, has significantly expanded therapeutic options and improved outcomes for patients with BPDCN. However, its use can be accompanied by notable adverse events, especially capillary leak syndrome, underscoring the need for careful patient selection and monitoring. Up to date, no data is available regarding the safety of tagraxofusp in patients with chronic kidney failure and cardiovascular co-morbidities. We present the case of a 79-year-old male who developed a solitary, rapidly progressing skin lesion on his lower back. The lesion represented the first manifestation of BPDCN with bone marrow infiltration and concomitant myelodysplastic syndrome (MDS). Molecular analysis identified mutations in CBL, TET2, ZRSR2 and KRAS. Non-eligible for stem cell transplantation, the patient was admitted to treatment with tagraxofusp in a dose-reduced protocol due to concomitant chronic kidney disease (CKD). After three doses of the first cycle, treatment needed to be stopped due to acute-on-chronic renal failure. After treatment disruption, kidney failure was completely restituted to pre-treatment levels. Notably, skin and bone marrow biopsies demonstrated a dermatologic complete response and partial remission of bone marrow infiltration. A watch and wait concept was followed, and prolonged therapy response was obtained for 8 months before relapse. To our knowledge, this is the first reported case demonstrating the use of tagraxofusp in a patient with BPDCN and advanced chronic kidney disease, showing that even a minimum of tolerated treatment dose can induce a sustained response. Despite the risk of adverse events, tagraxofusp should be considered a viable treatment option for elderly patients with poor performance status and significant comorbidities who are ineligible for intensive chemotherapy or stem cell transplantation, as even limited exposure may achieve meaningful clinical responses.

Indexed as

Blastic Plasmacytoid Dendritic Cell NeoplasmRecombinant Fusion ProteinsRenal Insufficiency, ChronicAgedHumansMaleRecombinant Fusion ProteinstagraxofuspBlastic plasmocytoid dendritic cell neoplasmCD123Diphteria toxinIL-3MDSTagraxofusp

Identifiers

PMID41535617
PMCPMC12804269

What Socratic 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 Socratic graph.