Evidence map›Paper›PMID 36583504›Full record

ReviewCancer medicine2023

Chimeric antigen receptor T (CAR-T) cells: Novel cell therapy for hematological malignancies.

Samane Abbasi, Milad Asghari Totmaj, Masoumeh Abbasi, Saba Hajazimian, Pouya Goleij, Javad Behroozi, Behrouz Shademan, Alireza Isazadeh, Behzad Baradaran

Open access · goldAbstract readReview
In one paragraph

Review in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 3 pooled it
8.4field-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

59 citing papers in PubMed, 3 syntheses or guidelines pooled it, 83 citations in OpenAlex.

  1. Pooled it
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  4. Recent advances in CAR T and CAR NK cell therapy for AML.International journal of hematology · 2026
    Review
  5. Article
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  8. Beyond cancer: CAR-T cells redefining liver disease therapy.JHEP reports : innovation in hepatology · 2026
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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

9 authors at 6 institutions in 3 countries.

Samane AbbasiDepartment of Biology, Faculty of Sciences, University of Guilan, Rasht, Iran.
Milad Asghari TotmajDepartment of Clinical Immunology, Faculty of Medicine, The University of Manchester, Manchester, UK.
Masoumeh AbbasiDepartment of Microbiology, Malekan Branch, Islamic Azad University, Malekan, Iran.
Saba HajazimianImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Pouya GoleijDepartment of Genetics, Faculty of Biology, Sana Institute of Higher Education, Sari, Iran.
Javad BehrooziDepartment of Genetics and Biotechnology, School of Medicine, AJA University of Medical Sciences, Tehran, Iran.
Behrouz ShademanDepartment of Medical Biology, Faculty of Medicine, Ege University, Izmir, Turkey.
Alireza IsazadehImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.ORCID 0000-0002-8781-1177
Behzad BaradaranImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.ORCID 0000-0002-8642-6795
Tabriz University of Medical Sciences · IRAja University of Medical Sciences · IREge University · TRIslamic Azad University, Tehran · IRUniversity of Guilan · IRUniversity of Manchester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the last decade, the emergence of several novel therapeutic approaches has changed the therapeutic perspective of human malignancies. Adoptive immunotherapy through chimeric antigen receptor T cell (CAR-T), which includes the engineering of T cells to recognize tumor-specific membrane antigens and, as a result, death of cancer cells, has created various clinical benefits for the treatment of several human malignancies. In particular, CAR-T-cell-based immunotherapy is known as a critical approach for the treatment of patients with hematological malignancies such as acute lymphoblastic leukemia (ALL), multiple myeloma (MM), chronic lymphocytic leukemia (CLL), acute myeloid leukemia (AML), Hodgkin lymphoma (HL), and non-Hodgkin's lymphoma (NHL). However, CAR-T-cell therapy of hematological malignancies is associated with various side effects. There are still extensive challenges in association with further progress of this therapeutic approach, from manufacturing and engineering issues to limitations of applications and serious toxicities. Therefore, further studies are required to enhance efficacy and minimize adverse events. In the current review, we summarize the development of CAR-T-cell-based immunotherapy and current clinical antitumor applications to treat hematological malignancies. Furthermore, we will mention the current advantages, disadvantages, challenges, and therapeutic limitations of CAR-T-cell therapy.

Indexed as

Hematologic NeoplasmsMultiple MyelomaReceptors, Chimeric AntigenAntigens, NeoplasmCell- and Tissue-Based TherapyHumansImmunotherapy, AdoptiveAntigens, NeoplasmReceptors, Chimeric Antigenchimeric antigen receptor T cellshematological malignanciesimmune therapyT-cell therapytumor immunology

Identifiers

PMID36583504
PMCPMC10134288
OpenAlexW4313312966

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.