Evidence map›Paper›PMID 29730801›Full record

ReviewMedical oncology (Northwood, London, England)2018

Challenges and prospects of chimeric antigen receptor T cell therapy in solid tumors.

Vishal Jindal, Ena Arora, Sorab Gupta

Abstract readReview
PubMed Publisher
In one paragraph

Review in Medical oncology (Northwood, London, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Car T Cells in Solid Tumors: Overcoming Obstacles.International journal of molecular sciences · 2024
    Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Current status and hurdles for CAR-T cell immune therapy.Blood science (Baltimore, Md.) · 2019
    Article
  18. Article
  19. Review
  20. Low-Dose Radiation Conditioning Enables CAR T Cells to Mitigate Antigen Escape.Molecular therapy : the journal of the American Society of Gene Therapy · 2018
    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

3 authors at 3 institutions in 2 countries.

Vishal JindalDepartment of Internal Medicine, Saint Vincent Hospital, 123 Summer Street, Worcester, MA, 01608, USA. vishaljindal87@gmail.com.ORCID http://orcid.org/0000-0001-9265-0251
Ena AroraDepartment of Internal Medicine, Government Medical College, Chandigarh, India.
Sorab GuptaDepartment of Hematology and Oncology, Einstein Healthcare Network, Philadelphia, USA.
Einstein Healthcare Network · USGovernment Medical College · INSaint Vincent Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor (CAR) T cell therapy is a novel and innovative immunotherapy. CAR-T cells are genetically engineered T cells, carrying MHC independent specific antigen receptor and co-stimulatory molecule which can activate an immune response to a cancer specific antigen. This therapy showed great results in hematological malignancies but were unable to prove their worth in solid tumors. Likely reasons for their failure are lack of antigens, poor trafficking, and hostile tumor microenvironment. Excessive amount of research is going on to improve the efficacy of CAR T cell therapy in solid tumors. In this article, we will discuss the challenges faced in improving the outcome of CAR T cell therapy in solid tumors and various strategies adopted to curb them.

Indexed as

AnimalsHumansImmunotherapy, AdoptiveNeoplasmsReceptors, Antigen, T-CellT-LymphocytesReceptors, Antigen, T-CellChimeric antigen receptor T cell therapyImmunotherapySolid tumors

Identifiers

PMID29730801
OpenAlexW2801359883

What OpenQuestion holds

Textmetadata
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.