Evidence map›Paper›PMID 35846081›Full record

ArticleEJHaem2021

BPDCN: When polychemotherapy does not compromise allogeneic CD123 CAR-T cell cytotoxicity.

Margaux Poussard, Laure Philippe, Maxime Fredon, Elodie Bôle-Richard, Sabeha Biichle, Florian Renosi, Sophie Perrin, Marie Kroemer, Samuel Limat, Francis Bonnefoy and 7 more

Open access · diamondAbstract readCase Reports
In one paragraph

Article in EJHaem, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 52% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

17 authors at 4 institutions in 2 countries.

Margaux PoussardINSERM EFS BFC UMR1098 RIGHT Interactions Greffon-Hôte Tumeur/Ingénierie Cellulaire et Génique Univ. Bourgogne Franche-Comté Besançon France.
Laure PhilippeService d'hématologie CH Annecy Genevois Metz-Tessy France.ORCID https://orcid.org/0000-0002-1121-2610
Maxime FredonINSERM EFS BFC UMR1098 RIGHT Interactions Greffon-Hôte Tumeur/Ingénierie Cellulaire et Génique Univ. Bourgogne Franche-Comté Besançon France.
Elodie Bôle-RichardINSERM EFS BFC UMR1098 RIGHT Interactions Greffon-Hôte Tumeur/Ingénierie Cellulaire et Génique Univ. Bourgogne Franche-Comté Besançon France.
Sabeha BiichleINSERM EFS BFC UMR1098 RIGHT Interactions Greffon-Hôte Tumeur/Ingénierie Cellulaire et Génique Univ. Bourgogne Franche-Comté Besançon France.
Florian RenosiINSERM EFS BFC UMR1098 RIGHT Interactions Greffon-Hôte Tumeur/Ingénierie Cellulaire et Génique Univ. Bourgogne Franche-Comté Besançon France.
Sophie PerrinPharmacy Department,CHRU Besançon University Hospital of Besançon Besançon France.
Marie KroemerPharmacy Department,CHRU Besançon University Hospital of Besançon Besançon France.
Samuel LimatPharmacy Department,CHRU Besançon University Hospital of Besançon Besançon France.
Francis BonnefoyINSERM EFS BFC UMR1098 RIGHT Interactions Greffon-Hôte Tumeur/Ingénierie Cellulaire et Génique Univ. Bourgogne Franche-Comté Besançon France.
Etienne DaguindauINSERM EFS BFC UMR1098 RIGHT Interactions Greffon-Hôte Tumeur/Ingénierie Cellulaire et Génique Univ. Bourgogne Franche-Comté Besançon France.
Eric DeconinckINSERM EFS BFC UMR1098 RIGHT Interactions Greffon-Hôte Tumeur/Ingénierie Cellulaire et Génique Univ. Bourgogne Franche-Comté Besançon France.ORCID https://orcid.org/0000-0002-6006-8088
Bérengère GrusonService d'hématologie CHU Amiens Amiens France.
Philippe SaasINSERM EFS BFC UMR1098 RIGHT Interactions Greffon-Hôte Tumeur/Ingénierie Cellulaire et Génique Univ. Bourgogne Franche-Comté Besançon France.
Olivier AdotéviINSERM EFS BFC UMR1098 RIGHT Interactions Greffon-Hôte Tumeur/Ingénierie Cellulaire et Génique Univ. Bourgogne Franche-Comté Besançon France.
Francine Garnache-OttouINSERM EFS BFC UMR1098 RIGHT Interactions Greffon-Hôte Tumeur/Ingénierie Cellulaire et Génique Univ. Bourgogne Franche-Comté Besançon France.
Fanny Angelot-DelettreINSERM EFS BFC UMR1098 RIGHT Interactions Greffon-Hôte Tumeur/Ingénierie Cellulaire et Génique Univ. Bourgogne Franche-Comté Besançon France.
Inserm · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire Amiens-Picardie · FRZero to Three · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare hematological malignancy with poor prognosis and no treatment consensus. Combining chemotherapy and immunotherapy is a promising strategy to enhance therapeutic effect. Before combining these therapies, the influence of one on the other has to be explored. We set up a model to test the combination of polychemotherapy - named methotrexate, idarubicine, dexamethasone, and L-asparaginase (MIDA) - and CD123 CAR-T cell therapy. We showed that CD123 CAR-T cells exert the same effect on BPDCN models alone, or after MIDA regimen. These data support a preclinical rationale to use immunotherapy after a treatment with polychemotherapy for BPDCN patients.

Indexed as

acute leukemiacell therapychemotherapyimmunologyT cells

Identifiers

PMID35846081
PMCPMC9176134
OpenAlexW3112195726

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.