Evidence map›Paper›PMID 20668228›Full record

Trial reportBlood2010

Eradication of B-lineage cells and regression of lymphoma in a patient treated with autologous T cells genetically engineered to recognize CD19.

James N Kochenderfer, Wyndham H Wilson, John E Janik, Mark E Dudley, Maryalice Stetler-Stevenson, Steven A Feldman, Irina Maric, Mark Raffeld, Debbie-Ann N Nathan, Brock J Lanier and 2 more

2 registry-linked trialsOpen access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 770 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
770citing papers in PubMed, 4 pooled it
30.3field-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.

NCT00924326 phase1 / phase2completednot on this map

An Assessment of the Safety and Feasibility of Administering T-Cells Expressing an Anti-CD19 Chimeric Antigen Receptor to Patients With B-Cell Lymphoma

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2009 to 2021Enrolled43ConditionsPrimary Mediastinal B-cell Lymphoma, Diffuse, Large B-cell Lymphoma, Diffuse Large B-Cell Lymphoma Transformed From Follicular Lymphoma, Mantle CellArmsFludarabine, Cyclophosphamide, Anti-cluster of differentiation 19 (CD19)-CAR PBL, Aldesleukin
NCT01593696 phase1completednot on this mapstarted 2012, after this paper: background citation

Phase I Study of T Cells Expressing an Anti-CD19 Chimeric Receptor in Children and Young Adults With B Cell Malignancies

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2012 to 2017Enrolled53ConditionsALL, B Cell Lymphoma, Leukemia, Large Cell LymphomaArmsAnti-Cluster of Differentiation (CD)19-Chimeric antigen receptor (CAR)
3 · Its place in the literature

Who cites it

770 citing papers in PubMed, 4 syntheses or guidelines pooled it, 1,329 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Letetresgene Autoleucel in Advanced/Metastatic Myxoid/Round Cell Liposarcoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025
    Trial
  7. Article
  8. Article
  9. Cardiotoxicity of T cell immunotherapies.Nature reviews. Cardiology · 2026
    Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Adoptive T-cell therapies in the clinic.Bioengineering & translational medicine · 2026
    Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. In vivo chimeric antigen receptor (CAR)-T cell therapy.Nature reviews. Drug discovery · 2026
    Review
  20. Review

710 more citing papers are in PubMed but not listed here.

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

12 authors at 3 institutions in 2 countries.

James N KochenderferSurgery Branch, National Cancer Institute, Bethesda, MD 20892, USA. kochendj@mail.nih.gov
Wyndham H Wilson
John E Janik
Mark E Dudley
Maryalice Stetler-Stevenson
Steven A Feldman
Irina Maric
Mark Raffeld
Debbie-Ann N Nathan
Brock J Lanier
Richard A Morgan
Steven A Rosenberg
Max Planck Institute for Metabolism Research · DENational Cancer Institute · USNational Institutes of Health Clinical Center · US

Funding

Flow Cytometric Analysis of Benign and Malignant TumorsZICSC009372 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI WANG, HAO-WEI · 2009 to 2025
$29.6M
Clinical production of viral vectors for cancer gene therapyZICBC010989 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BEYER, RACHEL · 2009 to 2025
$12.6M
Therapeutic Strategies and Molecular Correlates in Aggressive B-cell LymphomasZIASC006741 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI WILSON, WYNDHAM H · 2009 to 2025
$10.4M
Immunohistochemistry Core LaboratoryZICBC011087 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RAFFELD, MARK · 2009 to 2015
$7.4M
Cell Production Facility CoreZICBC011020 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DUDLEY, MARK · 2009 to 2013
$6.5M
Autologous T cells Transduced with an Anti-CD19 Chimeric Antigen ReceptorZIABC011413 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KOCHENDERFER, JAMES · 2011 to 2016
$731k
Bone Marrow Histopathological Changes in Neoplastic and Non-Neoplastic DiseasesZIACL090027 · CLC · CLINICAL CENTER · PI MARIC, IRINA · 2010 to 2025
$0k
Intramural NIH HHS
6 · The paper itself

Abstract

Adoptive transfer of genetically modified T cells is an attractive approach for generating antitumor immune responses. We treated a patient with advanced follicular lymphoma by administering a preparative chemotherapy regimen followed by autologous T cells genetically engineered to express a chimeric antigen receptor (CAR) that recognized the B-cell antigen CD19. The patient's lymphoma underwent a dramatic regression, and B-cell precursors were selectively eliminated from the patient's bone marrow after infusion of anti-CD19-CAR-transduced T cells. Blood B cells were absent for at least 39 weeks after anti-CD19-CAR-transduced T-cell infusion despite prompt recovery of other blood cell counts. Consistent with eradication of B-lineage cells, serum immunoglobulins decreased to very low levels after treatment. The prolonged and selective elimination of B-lineage cells could not be attributed to the chemotherapy that the patient received and indicated antigen-specific eradication of B-lineage cells. Adoptive transfer of anti-CD19-CAR-expressing T cells is a promising new approach for treating B-cell malignancies. This study is registered at www.clinicaltrials.gov as #NCT00924326.

Indexed as

Genetic EngineeringLymphocyte DepletionAntigens, CD19B-LymphocytesCell LineageHumansLymphomaMaleReceptors, AntigenRemission InductionT-LymphocytesTransduction, GeneticTransplantation, AutologousAntigens, CD19Receptors, Antigen

Identifiers

PMID20668228
PMCPMC2993617
OpenAlexW1966542058

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.