Evidence map›Paper›PMID 32731404›Full record

ReviewCancers2020

Innovative CAR-T Cell Therapy for Solid Tumor; Current Duel between CAR-T Spear and Tumor Shield.

Yuna Jo, Laraib Amir Ali, Ju A Shim, Byung Ha Lee, Changwan Hong

2 registry-linked trialsOpen access · goldAbstract readReview
In one paragraph

Review in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-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.

NCT05621486 phase1active not recruitingnot on this mapstarted 2022, after this paper: background citation

A FIH, Single Arm, Open Label Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Antitumor Activity of Autologous CAR T Cells Targeting BT-001 in Patients With Advanced Solid Tumors

TypeinterventionalSponsorShanghai East HospitalRan2022 to 2026Enrolled36ConditionsAdvanced Solid TumorArmsB4T2-001 Autologous CAR T cells
NCT06072989 phase1recruitingnot on this mapstarted 2023, after this paper: background citation

A Single Arm, Open Label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antitumor Activity of B4T2-001 CAR-T in Patients With Advanced Solid Tumors

TypeinterventionalSponsorShanghai East HospitalRan2023 to 2027Enrolled24ConditionsAdvanced Solid TumorArmsB4T2-001 autologous CAR-T
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. A tumor-conditional IL-15 safely synergizes with immunotherapy to enhance antitumor immune responses.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  4. Significant Advancements and Evolutions in Chimeric Antigen Receptor Design.International journal of molecular sciences · 2024
    Review
  5. Targeting ROS-sensing Nrf2 potentiates anti-tumor immunity of intratumoral CD8Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  6. Article
  7. Review
  8. Review
  9. Advances in CAR T Cell Therapy for Non-Small Cell Lung Cancer.Current issues in molecular biology · 2023
    Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Epigenetic strategies to boost CAR T cell therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Review
  17. Review
  18. Review
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 1 institution in 1 country.

Yuna JoDepartment of Anatomy, Pusan National University School of Medicine, Yangsan 50612, Korea.ORCID 0000-0002-5756-4873
Laraib Amir AliDepartment of Anatomy, Pusan National University School of Medicine, Yangsan 50612, Korea.ORCID 0000-0002-4664-718X
Ju A ShimDepartment of Anatomy, Pusan National University School of Medicine, Yangsan 50612, Korea.
Byung Ha LeeNeoImmuneTech, Inc., 2400 Research Blvd., Suite 250, Rockville, MD 20850, USA.
Changwan HongDepartment of Anatomy, Pusan National University School of Medicine, Yangsan 50612, Korea.ORCID 0000-0003-2567-2973
Pusan National University · KR

Funding

Pusan National University 2-Year Research Grant of Pusan National University
6 · The paper itself

Abstract

Novel engineered T cells containing chimeric antigen receptors (CAR-T cells) that combine the benefits of antigen recognition and T cell response have been developed, and their effect in the anti-tumor immunotherapy of patients with relapsed/refractory leukemia has been dramatic. Thus, CAR-T cell immunotherapy is rapidly emerging as a new therapy. However, it has limitations that prevent consistency in therapeutic effects in solid tumors, which accounts for over 90% of all cancer patients. Here, we review the literature regarding various obstacles to CAR-T cell immunotherapy for solid tumors, including those that cause CAR-T cell dysfunction in the immunosuppressive tumor microenvironment, such as reactive oxygen species, pH, O

Indexed as

CAR-Timmunotherapysolid tumorT cell responsestumor microenvironment

Identifiers

PMID32731404
PMCPMC7464778
OpenAlexW3046189784

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.