Evidence map›Paper›PMID 38673757›Full record

ReviewInternational journal of molecular sciences2024

Car T Cells in Solid Tumors: Overcoming Obstacles.

Joselyn Rojas-Quintero, María P Díaz, Jim Palmar, Nataly J Galan-Freyle, Valery Morillo, Daniel Escalona, Henry J González-Torres, Wheeler Torres, Elkin Navarro-Quiroz, Diego Rivera-Porras and 1 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
–field-weighted citation impact
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

40 citing papers in PubMed.

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  10. Imaging the fate of CAR-T cellsFrontiers in immunology · 2026
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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

11 authors.

Joselyn Rojas-QuinteroMedicine, Pulmonary, Critical Care, and Sleep Medicine Department, Baylor College of Medicine, Houston, TX 77030, USA.
María P DíazFacultad de Medicina, Centro de Investigaciones Endocrino-Metabólicas, Universidad del Zulia, Maracaibo 4001, Venezuela.
Jim PalmarFacultad de Medicina, Centro de Investigaciones Endocrino-Metabólicas, Universidad del Zulia, Maracaibo 4001, Venezuela.
Nataly J Galan-FreyleCentro de Investigaciones en Ciencias de la Vida, Universidad Simón Bolívar, Barranquilla 080002, Colombia.
Valery MorilloFacultad de Medicina, Centro de Investigaciones Endocrino-Metabólicas, Universidad del Zulia, Maracaibo 4001, Venezuela.
Daniel EscalonaFacultad de Medicina, Centro de Investigaciones Endocrino-Metabólicas, Universidad del Zulia, Maracaibo 4001, Venezuela.
Henry J González-TorresFacultad de Ciencias de la Salud, Universidad Simón Bolívar, Barranquilla 080002, Colombia.ORCID 0000-0001-7434-4568
Wheeler TorresFacultad de Medicina, Centro de Investigaciones Endocrino-Metabólicas, Universidad del Zulia, Maracaibo 4001, Venezuela.
Elkin Navarro-QuirozCentro de Investigaciones en Ciencias de la Vida, Universidad Simón Bolívar, Barranquilla 080002, Colombia.ORCID 0000-0001-7567-6409
Diego Rivera-PorrasFacultad de Ciencias Jurídicas y Sociales, Universidad Simón Bolívar, Cúcuta 540001, Colombia.ORCID 0000-0003-2169-3208
Valmore BermúdezCentro de Investigaciones en Ciencias de la Vida, Universidad Simón Bolívar, Barranquilla 080002, Colombia.ORCID 0000-0003-1880-8887

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor T cell (CAR T cell) therapy has emerged as a prominent adoptive cell therapy and a therapeutic approach of great interest in the fight against cancer. This approach has shown notorious efficacy in refractory hematological neoplasm, which has bolstered its exploration in the field of solid cancers. However, successfully managing solid tumors presents considerable intrinsic challenges, which include the necessity of guiding the modified cells toward the tumoral region, assuring their penetration and survival in adverse microenvironments, and addressing the complexity of identifying the specific antigens for each type of cancer. This review focuses on outlining the challenges faced by CAR T cell therapy when used in the treatment of solid tumors, as well as presenting optimizations and emergent approaches directed at improving its efficacy in this particular context. From precise localization to the modulation of the tumoral microenvironment and the adaptation of antigen recognition strategies, diverse pathways will be examined to overcome the current limitations and buttress the therapeutic potential of CAR T cells in the fight against solid tumors.

Indexed as

Immunotherapy, AdoptiveNeoplasmsReceptors, Chimeric AntigenT-LymphocytesTumor MicroenvironmentAnimalsAntigens, NeoplasmHumansReceptors, Antigen, T-CellAntigens, NeoplasmReceptors, Antigen, T-CellReceptors, Chimeric Antigencancerimmunotherapysolid tumors

Identifiers

PMID38673757
PMCPMC11050550

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.