Evidence map›Paper›PMID 31738832›Full record

ArticleBlood advances2019

CAR T-cell therapy is effective for CD19-dim B-lymphoblastic leukemia but is impacted by prior blinatumomab therapy.

Vinodh Pillai, Kavitha Muralidharan, Wenzhao Meng, Asen Bagashev, Derek A Oldridge, Jaclyn Rosenthal, John Van Arnam, Jos J Melenhorst, Diwakar Mohan, Amanda M DiNofia and 12 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed, 3 pooled it
11.1field-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

106 citing papers in PubMed, 3 syntheses or guidelines pooled it, 199 citations in OpenAlex.

  1. Guideline
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  7. Article
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  15. CAR-T cells with the CD38Cell reports. Medicine · 2026
    Article
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  19. With BiTEs at the kiddie table, where do CARs come in for pediatric B-ALL?Hematology. American Society of Hematology. Education Program · 2025
    Review
  20. Review

46 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

22 authors at 4 institutions in 1 country.

Vinodh PillaiDepartment of Pathology and Laboratory Medicine and.
Kavitha MuralidharanPerelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Wenzhao MengDepartment of Pathology and Laboratory Medicine and.
Asen BagashevDepartment of Pathology and Laboratory Medicine and.
Derek A OldridgeDepartment of Pathology and Laboratory Medicine and.
Jaclyn RosenthalPerelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
John Van ArnamDepartment of Pathology and Laboratory Medicine and.
Jos J MelenhorstDepartment of Pathology and Laboratory Medicine and.
Diwakar MohanDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Amanda M DiNofiaDivision of Oncology, Cancer Immunotherapy Program, Children's Hospital of Philadelphia, Philadelphia, PA; and.
Minjie LuoDepartment of Pathology and Laboratory Medicine and.
Sindhu CherianDepartment of Laboratory Medicine, University of Washington, Seattle, WA.
Jonathan R FrommDepartment of Laboratory Medicine, University of Washington, Seattle, WA.
Gerald WertheimDepartment of Pathology and Laboratory Medicine and.
Andrei Thomas-TikhonenkoDepartment of Pathology and Laboratory Medicine and.
Michele PaesslerDepartment of Pathology and Laboratory Medicine and.
Carl H JuneDepartment of Pathology and Laboratory Medicine and.
Eline T Luning PrakDepartment of Pathology and Laboratory Medicine and.
Vijay G BhojDepartment of Pathology and Laboratory Medicine and.
Stephan A GruppDivision of Oncology, Cancer Immunotherapy Program, Children's Hospital of Philadelphia, Philadelphia, PA; and.
Shannon L MaudeDivision of Oncology, Cancer Immunotherapy Program, Children's Hospital of Philadelphia, Philadelphia, PA; and.
Susan R RheingoldDivision of Oncology, Cancer Immunotherapy Program, Children's Hospital of Philadelphia, Philadelphia, PA; and.
Children's Hospital of Philadelphia · USUniversity of Pennsylvania · USUniversity of Washington · USJohns Hopkins University · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
Project 3: Combinatorial and gene-editing approaches to enhance the efficacy of CAR T cell therapy of multiple myeloma.P01CA214278 · NCI · UNIVERSITY OF PENNSYLVANIA · PI CARL H. JUNE · 2017 to 2026
$26.8M
Cassette exons in neoplastic pro-B-cells: implications for immunotherapyU01CA232563 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI BARASH, YOSEPH, THOMAS-TIKHONENKO, ANDREI · 2018 to 2022
$3.5M
NCI NIH HHS P01 CA214278NCI NIH HHS P30 CA016520NCI NIH HHS U01 CA232563
6 · The paper itself

Abstract

Tisagenlecleucel, a chimeric antigen receptor (CAR) T-cell product targeting CD19 is approved for relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL). However, the impact of pretreatment variables, such as CD19 expression level, on leukemic blasts, the presence of CD19- subpopulations, and especially prior CD19-targeted therapy, on the response to CAR T-cell therapy has not been determined. We analyzed 166 patients treated with CAR T-cell therapy at our institution. Eleven patients did not achieve a minimal residual disease (MRD)- deep remission, whereas 67 patients had a recurrence after achieving a MRD- deep remission: 28 patients with CD19+ leukemia and 39 patients with CD19- leukemia. Return of CD19+ leukemia was associated with loss of CAR T-cell function, whereas CD19- leukemia was associated with continued CAR T-cell function. There were no significant differences in efficacy of CAR T cells in CD19-dim B-ALL, compared with CD19-normal or -bright B-ALL. Consistent with this, CAR T cells recognized and lysed cells with very low levels of CD19 expression in vitro. The presence of dim CD19 or rare CD19- events by flow cytometry did not predict nonresponse or recurrence after CAR T-cell therapy. However, prior therapy with the CD19-directed, bispecific T-cell engager blinatumomab was associated with a significantly higher rate of failure to achieve MRD- remission or subsequent loss of remission with antigen escape. Finally, immunophenotypic heterogeneity and lineage plasticity were independent of underlying clonotype and cytogenetic abnormalities.

Indexed as

Immunotherapy, AdoptiveAdolescentAdultAntibodies, BispecificAntigens, CD19Antineoplastic Agents, ImmunologicalChildChild, PreschoolCombined Modality TherapyCytotoxicity, ImmunologicFemaleHumansImmunophenotypingInfantMaleNeoplasm, ResidualAntibodies, BispecificAntigens, CD19Antineoplastic Agents, ImmunologicalblinatumomabCD19-specific chimeric antigen receptorReceptors, Antigen, T-Cell

Identifiers

PMID31738832
PMCPMC6880911
OpenAlexW2985081230

What OpenQuestion holds

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Registered trials

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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.