Evidence map›Paper›PMID 37507426›Full record

ArticleLeukemia2023

WT1 and PRAME RNA-loaded dendritic cell vaccine as maintenance therapy in de novo AML after intensive induction chemotherapy.

Yngvar Fløisand, Mats Remberger, Iris Bigalke, Dag Josefsen, Helen Vålerhaugen, Else Marit Inderberg, Richard W Olaussen, Bjørn Tore Gjertsen, Rene Goedkoop, Christiane Geiger and 5 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Shared PRAME epitopes are T-cell targets in NUT carcinoma.Journal for immunotherapy of cancer · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Assembling the RNA therapeutics toolbox.Medical review (2021) · 2024
    Review
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  15. Review
  16. Review
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 4 institutions in 3 countries.

Yngvar FløisandCentre for Cancer Cell Reprogramming, Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway. yfl70@me.com.ORCID 0000-0001-7267-1944
Mats RembergerDepartment of Hematology, Oslo University Hospital, Oslo, Norway.
Iris BigalkeDepartment of Cellular Therapy, Oslo University Hospital, Oslo, Norway.
Dag JosefsenDepartment of Cellular Therapy, Oslo University Hospital, Oslo, Norway.
Helen VålerhaugenDepartment of Pathology, Oslo University Hospital, Oslo, Norway.
Else Marit InderbergDepartment of Cellular Therapy, Oslo University Hospital, Oslo, Norway.
Richard W OlaussenDepartment of Cellular Therapy, Oslo University Hospital, Oslo, Norway.
Bjørn Tore GjertsenDepartment of Clinical Science, University of Bergen; Department of Medicine, Hematology Section, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0001-9358-9704
Rene GoedkoopMedigene Immunotherapies GmbH and Medigene AG, Martinsried, Germany.
Christiane GeigerMedigene Immunotherapies GmbH and Medigene AG, Martinsried, Germany.
Petra U PrinzMedigene Immunotherapies GmbH and Medigene AG, Martinsried, Germany.
Frauke M SchnorfeilMedigene Immunotherapies GmbH and Medigene AG, Martinsried, Germany.
Kai PinkernellMedigene Immunotherapies GmbH and Medigene AG, Martinsried, Germany.
Dolores J SchendelMedigene Immunotherapies GmbH and Medigene AG, Martinsried, Germany.ORCID 0000-0003-2466-2976
Gunnar KvalheimDepartment of Cellular Therapy, Oslo University Hospital, Oslo, Norway.
Oslo University Hospital · NOMedigene (Germany) · DEHaukeland University Hospital · NOUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intensive induction chemotherapy achieves complete remissions (CR) in >60% of patients with acute myeloid leukemia (AML) but overall survival (OS) is poor for relapsing patients not eligible for allogeneic hematopoietic stem cell transplantation (allo-HSCT). Oral azacytidine may be used as maintenance treatment in AML in first remission, but can be associated with substantial side effects, and less toxic strategies should be explored. Twenty AML patients in first CR (CR1) ineligible for allo-HSCT were treated with FDC101, an autologous RNA-loaded mature dendritic cell (mDC) vaccine expressing two leukemia-associated antigens (LAAs). Each dose consisted of 2.5-5 × 10

Indexed as

Hematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteAntigens, NeoplasmDendritic CellsHumansInduction ChemotherapyRecurrenceRemission InductionRetrospective StudiesTransplantation, HomologousWT1 ProteinsAntigens, NeoplasmPRAME protein, humanWT1 protein, humanWT1 Proteins

Identifiers

PMID37507426
OpenAlexW4385334594

What OpenQuestion holds

Textmetadata
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.