Evidence map›Paper›PMID 35280988›Full record

ReviewFrontiers in immunology2022

CD19-Targeted Immunotherapies for Diffuse Large B-Cell Lymphoma.

Massimiliano Gambella, Simona Carlomagno, Anna Maria Raiola, Livia Giannoni, Chiara Ghiggi, Chiara Setti, Chiara Giordano, Silvia Luchetti, Alberto Serio, Alessandra Bo and 4 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

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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

14 authors at 3 institutions in 1 country.

Massimiliano GambellaEmatologia e Terapie Cellulari, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Simona CarlomagnoDepartment of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.
Anna Maria RaiolaEmatologia e Terapie Cellulari, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Livia GiannoniEmatologia e Terapie Cellulari, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Chiara GhiggiEmatologia e Terapie Cellulari, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Chiara SettiDepartment of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.
Chiara GiordanoDepartment of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.
Silvia LuchettiEmatologia e Terapie Cellulari, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Alberto SerioEmatologia e Terapie Cellulari, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Alessandra BoEmatologia e Terapie Cellulari, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Michela FalcoLaboratory of Clinical and Experimental Immunology, Integrated Department of Services and Laboratories, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Mariella Della ChiesaDepartment of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.
Emanuele AngelucciEmatologia e Terapie Cellulari, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Simona SivoriDepartment of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.
Ospedale Policlinico San Martino · ITUniversity of Genoa · ITIstituti di Ricovero e Cura a Carattere Scientifico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Surgical resection, chemotherapy and radiotherapy were, for many years, the only available cancer treatments. Recently, the use of immune checkpoint inhibitors and adoptive cell therapies has emerged as promising alternative. These cancer immunotherapies are aimed to support or harness the patient's immune system to recognize and destroy cancer cells. Preclinical and clinical studies, based on the use of T cells and more recently NK cells genetically modified with chimeric antigen receptors retargeting the adoptive cell therapy towards tumor cells, have already shown remarkable results. In this review, we outline the latest highlights and progress in immunotherapies for the treatment of Diffuse Large B-cell Lymphoma (DLBCL) patients, focusing on CD19-targeted immunotherapies. We also discuss current clinical trials and opportunities of using immunotherapies to treat DLBCL patients.

Indexed as

Lymphoma, Large B-Cell, DiffuseReceptors, Chimeric AntigenAntigens, CD19HumansImmunotherapyImmunotherapy, AdoptiveAntigens, CD19Receptors, Chimeric Antigenantibody-drug conjugatesbispecific T cell engagersCAR-NK cellsCAR-T cellsengineered T cellsgenetic modificationmonoclonal antibodies

Identifiers

PMID35280988
PMCPMC8911710
OpenAlexW4213412860

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.