Evidence map›Paper›PMID 31690821›Full record

ReviewLeukemia2019

CD19 chimeric antigen receptor-T cells in B-cell leukemia and lymphoma: current status and perspectives.

Mohamad Mohty, Jordan Gautier, Florent Malard, Mahmoud Aljurf, Ali Bazarbachi, Christian Chabannon, Mohamed A Kharfan-Dabaja, Bipin N Savani, He Huang, Saad Kenderian and 2 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Leukemia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 4 pooled it
4.5field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 4 syntheses or guidelines pooled it, 64 citations in OpenAlex.

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  11. Acute lymphoblastic leukaemia.Nature reviews. Disease primers · 2024
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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 10 institutions in 6 countries.

Mohamad MohtyService d'Hématologie Clinique et Thérapie Cellulaire, Hôpital Saint-Antoine, Sorbonne Université, INSERM UMRs 938, Paris, France. mohamad.mohty@inserm.fr.
Jordan GautierClinical Research Division, Integrated Immunotherapy Research Center, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-5769-8409
Florent MalardService d'Hématologie Clinique et Thérapie Cellulaire, Hôpital Saint-Antoine, Sorbonne Université, INSERM UMRs 938, Paris, France.ORCID http://orcid.org/0000-0002-3474-0002
Mahmoud AljurfOncology Center, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.
Ali BazarbachiDepartment of Internal Medicine/ American University of Beirut, Beirut, Lebanon.
Christian ChabannonInstitut Paoli-Calmettes, Inserm CBT-1409 & Aix-Marseille Université, Marseille, France.ORCID http://orcid.org/0000-0002-3755-4889
Mohamed A Kharfan-DabajaBlood and Marrow Transplantation Program, Division of Hematology-Oncology, Mayo Clinic, Jacksonville, FL, USA.ORCID http://orcid.org/0000-0001-7394-5185
Bipin N SavaniHematology and Stem Cell Transplantation Section, Division of Hematology/Oncology, Department of Medicine, Vanderbilt University Medical Center and Veterans Affairs Medical Center, Nashville, TN, USA.ORCID http://orcid.org/0000-0002-3304-9965
He HuangBone Marrow Transplantation Center, the First Affiliated Hospital, School of Medicine, Zhejiang University, Institute of Hematology, Zhejiang Province Engineering Laboratory for Stem Cell and Immunity Therapy, Hangzhou, 310058, China.
Saad KenderianDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.
Arnon NaglerThe Chaim Sheba Medical Center, Tel-Hashomer, Affiliated with the Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Miguel-Angel PeralesAdult Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Inserm · FRAmerican University of Beirut · LBFred Hutch Cancer Center · USKing Faisal Specialist Hospital & Research Centre · SAMayo Clinic in Arizona · USMayo Clinic in Florida · USMemorial Sloan Kettering Cancer Center · USTel Aviv University · ILVanderbilt University Medical Center · USZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The approval of tisagenlecleucel and axicabtagene ciloleucel represents a breakthrough in the field of immune and cellular therapy for hematologic malignancies. These anti-CD19 chimeric antigen receptor-T cells (CAR) proved to be highly effective in the treatment of relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL) and specific histologic subtypes of B-cell non-Hodgkin lymphomas. This expert review aims to summarize the current available research evidence in this field, with a special focus on the different challenges faced by treating physicians, and we also provide future perspectives.

Indexed as

Immunotherapy, AdoptiveAntigens, CD19Antigens, NeoplasmBiomarkers, TumorClinical Trials as TopicGenetic EngineeringHumansLeukemia, B-CellLymphoma, B-CellReceptors, Chimeric AntigenT-LymphocytesTreatment OutcomeAntigens, CD19Antigens, NeoplasmBiomarkers, TumorCD19 molecule, humanReceptors, Chimeric Antigen

Identifiers

PMID31690821
OpenAlexW2983077705

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.