Evidence map›Paper›PMID 35468946›Full record

ArticleLeukemia2022

CD19 CAR T-cells for pediatric relapsed acute lymphoblastic leukemia with active CNS involvement: a retrospective international study.

Elad Jacoby, Sara Ghorashian, Britta Vormoor, Barbara De Moerloose, Nicole Bodmer, Olga Molostova, Asaf D Yanir, Jochen Buechner, Ronit Elhasid, Bella Bielorai and 11 more

Abstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
6.2field-weighted citation impact, top 2% 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

39 citing papers in PubMed, 62 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Haematologica · 2025
    Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. 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

21 authors at 13 institutions in 10 countries.

Elad JacobyThe Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel. Elad.jacoby@sheba.health.gov.il.ORCID http://orcid.org/0000-0003-1411-8942
Sara GhorashianDevelopmental Biology and Cancer, UCL Great Ormond Street Institute of Child Health, London, ENG, UK.
Britta VormoorPrincess Maxima Center for Paediatric Oncology, Utrecht, Netherlands.
Barbara De MoerlooseDept of Pediatric Hematology-Oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent, Belgium.
Nicole BodmerUniversity Children's Hospital Zürich, Zürich, Switzerland.
Olga MolostovaDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russian Federation.
Asaf D YanirSackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Jochen BuechnerDepartment of Pediatric Hematology and Oncology, Oslo University Hospital, Oslo, Norway.ORCID http://orcid.org/0000-0001-5848-4501
Ronit ElhasidSackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.ORCID http://orcid.org/0000-0002-5663-6919
Bella BieloraiThe Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
Srdan RogosicDevelopmental Biology and Cancer, UCL Great Ormond Street Institute of Child Health, London, ENG, UK.
Marie-Emilie DourtheDepartment of Pediatric Hematology and Immunology, University Hospital Robert Debré (APHP) and Université de Paris, Paris, France.
Michael MaschanDmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russian Federation.ORCID http://orcid.org/0000-0003-1735-0093
Claudia RossigPediatric Hematology and Oncology, University Children's Hospital Muenster, Muenster, Germany.
Amos TorenThe Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
Arend von StackelbergDepartment of Pediatric Oncology/Hematology, Charite Medical Center, Berlin, Germany.
Franco LocatelliDepartment of Hematology and Oncology and Cell and Gene Therapy, IRCCS Bambino Gesù Children's Hospital, Rome, Sapienza, University of Rome, Rome, Italy.
Peter BaderDivision for Stem Cell Transplantation and Immunology, Department for Children and Adolescents, University Hospital Frankfurt, Goethe University, Frankfurt am Main, Germany.ORCID http://orcid.org/0000-0003-4554-0265
Martin ZimmermannPediatric Hematology and Oncology, Hannover Medical School, Hannover, Germany.
Jean Pierre BourquinUniversity Children's Hospital Zürich, Zürich, Switzerland.
Andre BaruchelDepartment of Pediatric Hematology and Immunology, University Hospital Robert Debré (APHP) and Université de Paris, Paris, France. Andre.baruchel@aphp.fr.ORCID http://orcid.org/0000-0003-0120-6089
Tel Aviv University · ILDmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology · RUGreat Ormond Street Hospital · GBUniversité Paris Cité · FRUniversity Children's Hospital Zurich · CHBambino Gesù Children's Hospital · ITCharité - Universitätsmedizin Berlin · DEGhent University Hospital · BEGoethe University Frankfurt · DEMedizinische Hochschule Hannover · DEOslo University Hospital · NOPrincess Máxima Center · NLUniversity Hospital Münster · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Relapse of B-cell precursor acute lymphoblastic leukemia (BCP-ALL) may occur in the central nervous system (CNS). Most clinical trials of CAR T-cell therapy excluded patients with active CNS leukemia, partially for concerns of neurotoxicity. Here, we report an international study of fifty-five children and adolescents who received CAR T-cell therapy for relapsed BCP-ALL with CNS involvement at the time of referral. All patients received bridging therapy, 16 still having active CNS disease at the time of lymphodepletion. Twelve patients received CD28-based CAR T-cells, 9 being subsequently treated with allogeneic hematopoietic stem-cell transplantation (allo-HSCT). Forty-three patients received 4-1BB-based CAR T-cells. Cytokine-release syndrome (CRS) and neurotoxicity occurred in 65% and 38% of patients, respectively, more frequently following treatment with CD28-based CARs. Fifty-one of 54 evaluable patients (94%) achieved complete response following this therapy. Relapse occurred in 22 patients: 19/43 following 4-1BB-based CARs (12 CNS relapses), and 3/12 after CD28-based CARs with subsequent HSCT (no CNS relapse). Patients treated with tisagenlecleucel for an isolated CNS relapse had a high incidence of a subsequent CNS relapse (6 of 8). CAR T-cells were found to be effective in this cohort, though the risk of CNS relapse was not completely mitigated by this approach.

Indexed as

Hematopoietic Stem Cell TransplantationPrecursor Cell Lymphoblastic Leukemia-LymphomaReceptors, Chimeric AntigenAdaptor Proteins, Signal TransducingAdolescentAntigens, CD19CD28 AntigensChildHumansImmunotherapy, AdoptiveRecurrenceRetrospective StudiesT-LymphocytesAdaptor Proteins, Signal TransducingAntigens, CD19CD28 AntigensReceptors, Chimeric Antigen

Identifiers

PMID35468946
OpenAlexW4224935414

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.