Evidence map›Paper›PMID 32594314›Full record

ReviewInternational journal of hematology2021

Next-generation CAR T cells to overcome current drawbacks.

Stefan Lundh, Sayantan Maji, J Joseph Melenhorst

Abstract readReview
PubMed Publisher
In one paragraph

Review in International journal of hematology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The Evolving Landscape of Potency Assays.Advances in experimental medicine and biology · 2023
    Article
  5. Review
  6. Review
  7. Article
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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

3 authors at 2 institutions in 1 country.

Stefan LundhCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA, USA.
Sayantan MajiCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA, USA.
J Joseph MelenhorstCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA, USA. mej@pennmedicine.upenn.edu.ORCID http://orcid.org/0000-0001-7677-537X
University of Pennsylvania · USParker Institute for Cancer Immunotherapy · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As a rapidly emerging treatment in the oncology field, adoptive transfer of autologous, genetically modified chimeric antigen receptor (CAR) T cells has shown striking efficacy and is curative in certain relapsed/refractory patients with hematologic malignancy. This treatment modality of using a "living drug" offers many tantalizing and novel therapeutic strategies for cancer patients whose remaining treatment options may have otherwise been limited. Despite the early success of CAR T cells in hematologic malignancies, many barriers remain for widespread adoption. General barriers include cellular manufacturing limitations, baseline quality of the T cells, adverse events post-infusion such as cytokine release syndrome (CRS) and neurotoxicity, and host rejection of non-human CARs. Additionally, each hematologic disease presents unique mechanisms of relapse which have to be addressed in future clinical trials if we are to augment the efficacy of CAR T treatment. In this review, we will describe current barriers to hindering efficacy of CAR T-cell treatment for hematologic malignancies in a disease-specific manner and review recent innovations aimed at enhancing the potency and applicability of CAR T cells, with the overall goal of building a framework to begin incorporating this form of therapy into the standard medical management of blood cancers.

Indexed as

AnimalsCombined Modality TherapyDisease ManagementDisease SusceptibilityHumansImmunotherapy, AdoptiveNeoplasmsPrognosisReceptors, Antigen, T-CellReceptors, Chimeric AntigenT-LymphocytesTreatment OutcomeReceptors, Antigen, T-CellReceptors, Chimeric AntigenCancerCAR T cellChimeric antigen receptorImmunotherapy

Identifiers

PMID32594314
OpenAlexW3037557840

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.