Evidence map›Paper›PMID 35757715›Full record

ReviewFrontiers in immunology2022

CAR-T Cell Therapy in Hematological Malignancies: Current Opportunities and Challenges.

Xiaomin Zhang, Lingling Zhu, Hui Zhang, Shanshan Chen, Yang Xiao

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 272 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
272citing papers in PubMed, 7 pooled it
32.4field-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

272 citing papers in PubMed, 7 syntheses or guidelines pooled it, 339 citations in OpenAlex.

  1. Pooled it
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  4. Application of CAR-T cell therapy in B-cell lymphoma: a meta-analysis of randomized controlled trials.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
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  15. Lnk Governs chemokine-directed trafficking of CD8Molecular therapy. Oncology · 2026
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  17. The logarithmic phase as a therapeutic direction: evaluating pharmacological strategies against cancer progression.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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212 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

5 authors at 4 institutions in 1 country.

Xiaomin ZhangDepartment of Hematology, Jinshazhou Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.
Lingling ZhuCancer Center, Integrated Hospital of Traditional Chinese Medicine, Southern Medical University, Guangzhou, China.
Hui ZhangSchool of Medicine, Jishou University, Jishou, China.
Shanshan ChenCancer Center, Integrated Hospital of Traditional Chinese Medicine, Southern Medical University, Guangzhou, China.
Yang XiaoInstitute of Clinical Medicine College, Guangzhou University of Chinese Medicine, Guangzhou, China.
TCM-Intigrated Cancer Center of Southern Medical University · CNGuangzhou Development Zone Hospital · CNGuangzhou University of Chinese Medicine · CNJishou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor T (CAR-T) cell therapy represents a major breakthrough in cancer treatment, and it has achieved unprecedented success in hematological malignancies, especially in relapsed/refractory (R/R) B cell malignancies. At present, CD19 and BCMA are the most common targets in CAR-T cell therapy, and numerous novel therapeutic targets are being explored. However, the adverse events related to CAR-T cell therapy might be serious or even life-threatening, such as cytokine release syndrome (CRS), CAR-T-cell-related encephalopathy syndrome (CRES), infections, cytopenia, and CRS-related coagulopathy. In addition, due to antigen escape, the limited CAR-T cell persistence, and immunosuppressive tumor microenvironment, a considerable proportion of patients relapse after CAR-T cell therapy. Thus, in this review, we focus on the progress and challenges of CAR-T cell therapy in hematological malignancies, such as attractive therapeutic targets, CAR-T related toxicities, and resistance to CAR-T cell therapy, and provide some practical recommendations.

Indexed as

Hematologic NeoplasmsReceptors, Chimeric AntigenCell- and Tissue-Based TherapyCytokine Release SyndromeHumansImmunotherapy, AdoptiveNeoplasm Recurrence, LocalTumor MicroenvironmentReceptors, Chimeric Antigenantigen escapeCAR-T cellCAR-T related toxicitiescombinatorial therapyhematological malignanciesimmunosuppressive tumor microenvironment

Identifiers

PMID35757715
PMCPMC9226391
OpenAlexW4281961745

What OpenQuestion holds

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LicenceCC BY
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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.