Evidence map›Paper›PMID 42527665›Full record

ReviewLeukemia2026

Stuck in traffic: CART cells targeting the tumor microenvironment in hematological malignancies, current advances and future perspectives.

Jennifer Meyer Feigin, Elizabeth L Siegler, Saad S Kenderian

Abstract readReview
PubMed Publisher
In one paragraph

Review in Leukemia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jennifer Meyer FeiginT Cell Engineering Lab, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0009-0000-6499-4655
Elizabeth L SieglerT Cell Engineering Lab, Mayo Clinic, Rochester, MN, USA.
Saad S KenderianT Cell Engineering Lab, Mayo Clinic, Rochester, MN, USA. Kenderian.saad@mayo.edu.ORCID http://orcid.org/0000-0003-2767-3830

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor T cell (CART) therapy has revolutionized the treatment of B cell hematological malignancies, and has lead to several FDA-approved CART products beginning in 2017. However, while CART cell therapy has improved outcomes and survival, many patients eventually relapse after treatment. Research into the reasons for patient relapse following CART cell therapy has identified multiple mechanisms of resistance. These primarily include antigen loss, poor CART cell expansion or exhaustion, and tumor- or tumor-microenvironment (TME)-mediated immunosuppression of CART cells. While methods to study and engineer CART cells to circumvent antigenic loss or to prevent exhaustion are being investigated, the development of standalone or combination CART cell therapies that target both cancer cells and immunosuppressive components of the TME are less studied. In this review, we focus on the impact of the TME on CART cell efficacy in hematological malignancies and discuss promising basic and clinical approaches that may enable CART cells to overcome TME-mediated dysfunction.

Indexed as

Hematologic NeoplasmsImmunotherapy, AdoptiveReceptors, Chimeric AntigenT-LymphocytesTumor MicroenvironmentAnimalsHumansReceptors, Chimeric Antigen

Identifiers

What OpenQuestion holds

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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.