Evidence map›Paper›PMID 39042891›Full record

ReviewBlood advances2024

The rules of T-cell engagement: current state of CAR T cells and bispecific antibodies in B-cell lymphomas.

J Erika Haydu, Jeremy S Abramson

Abstract readReview
In one paragraph

Review in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–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

19 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

2 authors.

J Erika HayduCenter for Lymphoma, Mass General Cancer Center, Boston, MA.ORCID 0000-0003-2463-0560
Jeremy S AbramsonCenter for Lymphoma, Mass General Cancer Center, Boston, MA.ORCID 0000-0001-8467-9257

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractT-cell engaging-therapies have transformed the treatment landscape of relapsed and refractory B-cell non-Hodgkin lymphomas by offering highly effective treatments for patients with historically limited therapeutic options. This review focuses on the advances in chimeric antigen receptor-modified T cells and bispecific antibodies, first providing an overview of each product type, followed by exploring the primary data for currently available products in large B-cell lymphoma, follicular lymphoma, and mantle cell lymphoma. This review also highlights key logistical and sequencing considerations across diseases and product types that can affect clinical decision-making.

Indexed as

Antibodies, BispecificImmunotherapy, AdoptiveLymphoma, B-CellT-LymphocytesHumansReceptors, Chimeric AntigenAntibodies, BispecificReceptors, Chimeric Antigen

Identifiers

PMID39042891
PMCPMC11413679

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.