Evidence map›Paper›PMID 35860578›Full record

ReviewFrontiers in oncology2022

CAR-T Cells in the Treatment of Urologic Neoplasms: Present and Future.

Zhengchao Zhang, Dong Li, Heng Yun, Wei Liu, Keqiang Chai, Jie Tong, Tongwei Zeng, Zhenghua Gao, Yongqiang Xie

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Emerging molecular therapies in the treatment of bladder cancer.Exploration of targeted anti-tumor therapy · 2024
    Review
  9. Review
  10. Review
  11. Article
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 2 institutions in 1 country.

Zhengchao ZhangDepartment of Urology, The Third Affiliated Hospital of Gansu University of Traditional Chinese Medicine, Baiyin, China.
Dong LiDepartment of Urology, The Third Affiliated Hospital of Gansu University of Traditional Chinese Medicine, Baiyin, China.
Heng YunDepartment of Urology, The Third Affiliated Hospital of Gansu University of Traditional Chinese Medicine, Baiyin, China.
Wei LiuDepartment of Urology, The Third Affiliated Hospital of Gansu University of Traditional Chinese Medicine, Baiyin, China.
Keqiang ChaiDepartment of Urology, The Third Affiliated Hospital of Gansu University of Traditional Chinese Medicine, Baiyin, China.
Jie TongDepartment of Urology, The Third Affiliated Hospital of Gansu University of Traditional Chinese Medicine, Baiyin, China.
Tongwei ZengDepartment of Urology, The Third Affiliated Hospital of Gansu University of Traditional Chinese Medicine, Baiyin, China.
Zhenghua GaoDepartment of Urology, The Third Affiliated Hospital of Gansu University of Traditional Chinese Medicine, Baiyin, China.
Yongqiang XieDepartment of Urology, The Third Affiliated Hospital of Gansu University of Traditional Chinese Medicine, Baiyin, China.
Gansu University of Traditional Chinese Medicine · CNLanzhou University Second Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, with the breakthrough of CAR-T cells in the treatment of hematological tumors, they are increasingly being used to treat solid tumors, including urologic neoplasms. There are many relatively specific targets for urologic neoplasms, especially prostate cancer. Besides, urologic neoplasms tend to progress more slowly than tumors in other organs of the body, providing ample time for CAR-T cell application. Therefore, CAR-T cells technology has inherent advantages in urologic neoplasms. CAR-T cells in the treatment of urologic neoplasms have been extensively studied and preliminary achievements have been made. However, no breakthrough has been made due to the problems of targeting extra-tumor cytotoxicity and poor anti-tumor activity. we systematacially summarized the research actuality of CAR-T cells in urologic neoplasms, discussed the potential value and difficulties of the research. The application of CAR-T cells in the treatment of urologic neoplasms requires improvement of function through screening for better targets, modification of CAR structures, or in combination with other antitumor approaches.

Indexed as

bladder cancerCAR-T cellsimmunotherapykidney cancerprostate cancerurologic neoplasms

Identifiers

PMID35860578
PMCPMC9292130
OpenAlexW4283796967

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.