Evidence map›Paper›PMID 38491306›Full record

ArticleLeukemia2024

CD22 CAR T cells demonstrate high response rates and safety in pediatric and adult B-ALL: Phase 1b results.

Liora M Schultz, Nikeshan Jeyakumar, Anne Marijn Kramer, Bita Sahaf, Hrishi Srinagesh, Parveen Shiraz, Neha Agarwal, Mark Hamilton, Courtney Erickson, Ashley Jacobs and 27 more

Open access · bronzeAbstract readClinical Trial, Phase I
In one paragraph

Article in Leukemia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
10.2field-weighted citation impact, top 1% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Observational
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. CD22 as a Target for Hematological Malignancies and Autoimmune Diseases.International journal of molecular sciences · 2026
    Review
  9. Review
  10. Review
  11. Review
  12. Rational redesign of antigen binding domain improves in vivo efficacy of the CD22-CAR.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Sequence and structural determinants of efficaciousbioRxiv : the preprint server for biology · 2025
    Article
  20. 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

37 authors at 2 institutions in 1 country.

Liora M Schultz *Division of Pediatric Hematology/Oncology, Stanford University, Stanford, CA, USA.
Nikeshan Jeyakumar *Division of Hematology, Stanford University, Stanford, CA, USA.
Anne Marijn KramerCenter for Cancer Cell Therapy, Stanford University, Stanford, CA, USA.ORCID 0000-0001-5239-7343
Bita SahafCenter for Cancer Cell Therapy, Stanford University, Stanford, CA, USA.
Hrishi SrinageshDivision of Hematology, Stanford University, Stanford, CA, USA.
Parveen ShirazDivision of Blood and Marrow Transplantation and Cellular Therapy, Stanford University, Stanford, CA, USA.
Neha AgarwalDivision of Blood and Marrow Transplantation and Cellular Therapy, Stanford University, Stanford, CA, USA.
Mark HamiltonDivision of Hematology, Stanford University, Stanford, CA, USA.
Courtney EricksonDivision of Pediatric Hematology/Oncology, Stanford University, Stanford, CA, USA.
Ashley JacobsDivision of Pediatric Hematology/Oncology, Stanford University, Stanford, CA, USA.
Jennifer MoonDivision of Pediatric Hematology/Oncology, Stanford University, Stanford, CA, USA.
Christina BaggottDivision of Pediatric Hematology/Oncology, Stanford University, Stanford, CA, USA.
Sally AraiDivision of Blood and Marrow Transplantation and Cellular Therapy, Stanford University, Stanford, CA, USA.
Sushma BharadwajDivision of Blood and Marrow Transplantation and Cellular Therapy, Stanford University, Stanford, CA, USA.
Laura J JohnstonDivision of Blood and Marrow Transplantation and Cellular Therapy, Stanford University, Stanford, CA, USA.
Michaela LiedtkeDivision of Hematology, Stanford University, Stanford, CA, USA.
Robert LowskyDivision of Blood and Marrow Transplantation and Cellular Therapy, Stanford University, Stanford, CA, USA.
Everett MeyerDivision of Blood and Marrow Transplantation and Cellular Therapy, Stanford University, Stanford, CA, USA.
Robert NegrinDivision of Blood and Marrow Transplantation and Cellular Therapy, Stanford University, Stanford, CA, USA.
Andrew RezvaniDivision of Blood and Marrow Transplantation and Cellular Therapy, Stanford University, Stanford, CA, USA.
Judy ShizuruDivision of Blood and Marrow Transplantation and Cellular Therapy, Stanford University, Stanford, CA, USA.ORCID 0000-0003-3246-4726
Surbhi SidanaDivision of Blood and Marrow Transplantation and Cellular Therapy, Stanford University, Stanford, CA, USA.ORCID 0000-0003-3288-7614
Emily EgelerCenter for Cancer Cell Therapy, Stanford University, Stanford, CA, USA.
Sharon MavroukakisCenter for Cancer Cell Therapy, Stanford University, Stanford, CA, USA.
Ramya TunuguntlaLaboratory for Cell and Gene Medicine, Stanford University, Stanford, CA, USA.
Nikolaos Gkitsas-LongLaboratory for Cell and Gene Medicine, Stanford University, Stanford, CA, USA.
Aidan RetherfordLaboratory for Cell and Gene Medicine, Stanford University, Stanford, CA, USA.
Annie Kathleen BrownLaboratory for Cell and Gene Medicine, Stanford University, Stanford, CA, USA.
Anne-Louise Gramstrap-PetersenLaboratory for Cell and Gene Medicine, Stanford University, Stanford, CA, USA.
Raquel Martin IbañezLaboratory for Cell and Gene Medicine, Stanford University, Stanford, CA, USA.
Steven A FeldmanCenter for Cancer Cell Therapy, Stanford University, Stanford, CA, USA.
David B MiklosCenter for Cancer Cell Therapy, Stanford University, Stanford, CA, USA.ORCID 0000-0003-0717-4305
Crystal L MackallDivision of Pediatric Hematology/Oncology, Stanford University, Stanford, CA, USA.ORCID 0000-0001-6323-4304
Kara L DavisDivision of Pediatric Hematology/Oncology, Stanford University, Stanford, CA, USA.
Matthew FrankCenter for Cancer Cell Therapy, Stanford University, Stanford, CA, USA.
Sneha RamakrishnaDivision of Pediatric Hematology/Oncology, Stanford University, Stanford, CA, USA.
Lori MufflyCenter for Cancer Cell Therapy, Stanford University, Stanford, CA, USA. lmuffly@stanford.edu.ORCID 0000-0002-9887-6136
Stanford University · USStanford Blood Center · US

Funding

Lymphoma Antigen Density and Circulating Tumor DNA Profiling As Determinants of Novel CAR TherapiesK08CA248968 · NCI · STANFORD UNIVERSITY · PI FRANK, MATTHEW J. · 2020 to 2024
$845k
NCI NIH HHS K08 CA248968
6 · The paper itself

Abstract

Chimeric antigen receptor (CAR) T cells targeting CD22 (CD22-CAR) provide a therapeutic option for patients with CD22

Indexed as

Immunotherapy, AdoptivePrecursor B-Cell Lymphoblastic Leukemia-LymphomaReceptors, Chimeric AntigenSialic Acid Binding Ig-like Lectin 2AdolescentAdultChildChild, PreschoolFemaleHumansMaleMiddle AgedT-LymphocytesYoung AdultCD22 protein, humanReceptors, Chimeric AntigenSialic Acid Binding Ig-like Lectin 2

Identifiers

PMID38491306
PMCPMC12740236
OpenAlexW4392858002

What OpenQuestion holds

Textmetadata
LicenceTDM
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.