Evidence map›Paper›PMID 37664750›Full record

ReviewHeliyon2023

Chimeric antigen receptor-modified T cells therapy in prostate cancer: A comprehensive review on the current state and prospects.

Mingze He, Dongqi Zhang, Yu Cao, Changliang Chi, Zitong Zeng, Xinyi Yang, Guodong Yang, Kritika Sharma, Kebang Hu, Mikhail Enikeev

Open access · goldAbstract readReview
In one paragraph

Review in Heliyon, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

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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

10 authors at 2 institutions in 2 countries.

Mingze HeInstitute for Urology and Reproductive Health, I.M. Sechenov First Moscow State Medical University (Sechenov University), 119435, Moscow, Russia.
Dongqi ZhangDepartment of Urology, The First Hospital of Jilin University (Lequn Branch), 130000, Changchun, China.
Yu CaoI.M. Sechenov First Moscow State Medical University (Sechenov University), 119991, Moscow, Russia.
Changliang ChiDepartment of Urology, The First Hospital of Jilin University (Lequn Branch), 130000, Changchun, China.
Zitong ZengI.M. Sechenov First Moscow State Medical University (Sechenov University), 119991, Moscow, Russia.
Xinyi YangI.M. Sechenov First Moscow State Medical University (Sechenov University), 119991, Moscow, Russia.
Guodong YangI.M. Sechenov First Moscow State Medical University (Sechenov University), 119991, Moscow, Russia.
Kritika SharmaI.M. Sechenov First Moscow State Medical University (Sechenov University), 119991, Moscow, Russia.
Kebang HuDepartment of Urology, The First Hospital of Jilin University (Lequn Branch), 130000, Changchun, China.
Mikhail EnikeevInstitute for Urology and Reproductive Health, I.M. Sechenov First Moscow State Medical University (Sechenov University), 119435, Moscow, Russia.
Sechenov University · RUJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent immunotherapy research has focused on chimeric antigen receptor-modified T cells (CAR-Ts). CAR-T therapies have been clinically applied to manage hematologic malignancies with satisfactory effectiveness. However, the application of CAR-T immunotherapy in solid tumors remains challenging. Even so, current CAR-T immunotherapies for prostate cancer (PCa) have shown some promise, giving hope to patients with advanced metastatic PCa. This review aimed to elucidate different types of prostate tumor-associated antigen targets, such as prostate-specific membrane antigen and prostate stem cell antigen, and their effects. The current status of the corresponding targets in clinical research through their applications was also discussed. To improve the efficacy of CAR-T immunotherapy, we addressed the possible applications of multimodal immunotherapy, chemotherapy, and CAR-T combined therapies. The obstacles of solid tumors were concisely elaborated. Further studies should aim to discover novel potential targets and establish new models by overcoming the inherent barriers of solid tumors, such as tumor heterogeneity and the immunosuppressive nature of the tumor microenvironment.

Indexed as

CAR-TsImmunotherapyProstate cancerSolid tumorTumor-associated antigenTumor microenvironment

Identifiers

PMID37664750
PMCPMC10469587
OpenAlexW4386013427

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.