Evidence map›Paper›PMID 36275688›Full record

ArticleFrontiers in immunology2022

Case report: Senescence as mechanism of resistance to Pembrolizumab in a Lymphoma patient who failed CD19-Targeted CAR-T cell therapy.

Serena De Matteis, Beatrice Casadei, Ginevra Lolli, Michele Dicataldo, Francesco Barbato, Elisa Dan, Andrea Paccagnella, Barbara Sinigaglia, Clara Bertuzzi, Annalisa Arcari and 9 more

Open access · goldAbstract readCase Reports
In one paragraph

Article 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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

19 authors at 3 institutions in 1 country.

Serena De MatteisIRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Beatrice CasadeiIRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Ginevra LolliIRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Michele DicataldoIRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Francesco BarbatoIRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Elisa DanDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Bologna, Italy.
Andrea PaccagnellaDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Bologna, Italy.
Barbara SinigagliaDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Bologna, Italy.
Clara BertuzziIRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Annalisa ArcariHematology and Bone Marrow Transplant Unit, "Guglielmo da Saliceto" Hospital, Piacenza, Italy.
Luca ZazzeroniDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Bologna, Italy.
Patrizia BernuzziHematology and Bone Marrow Transplant Unit, "Guglielmo da Saliceto" Hospital, Piacenza, Italy.
Noemi LaproviteraIRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Gianluca StorciIRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Salvatore Nicola BertuccioDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.
Manuela FerracinDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Bologna, Italy.
Massimiliano BonafèDepartment of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Bologna, Italy.
Pier Luigi ZinzaniIRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Francesca BonifaziIRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
University of Bologna · ITAzienda USL di Bologna · ITGuglielmo da Saliceto Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: T cells engineered to target CD19 antigen on neoplastic B cells represent the most striking example of CAR-T cell therapy. The success rate of this therapy is affected by several limitations: target antigen loss, and/or acquisition of a senescent/exhausted phenotype by CAR and non-CAR T cells. Case presentation: We report on a patient affected by refractory Diffuse Large B-cell Lymphoma who was resistant to CAR T-cell therapy and to two cycles post CAR-T of pembrolizumab (PBZ) due to the evolution into a B-cell Hodgkin-like lymphoma. Owing to the CD30 expression and the Hodgkin-like phenotype, the patient was ultimately treated with Brentuximab-Vedotin and finally underwent remission. Upon PBZ treatment, 100% of circulating CAR-T Conclusions: PBZ is not able to reinvigorate exhausted CAR

Indexed as

Lymphoma, Large B-Cell, DiffuseReceptors, Chimeric AntigenAntibodies, Monoclonal, HumanizedAntigens, CD19CD8-Positive T-LymphocytesCell- and Tissue-Based TherapyHumansImmunotherapy, AdoptiveReceptors, Antigen, T-CellAntibodies, Monoclonal, HumanizedAntigens, CD19pembrolizumabReceptors, Antigen, T-CellReceptors, Chimeric Antigenchimeric antigen receptor (CAR T)exhaustionlymphomapembrolizumabresistancesenescence

Identifiers

PMID36275688
PMCPMC9584643
OpenAlexW4302299211

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.