Evidence map›Paper›PMID 37160803›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2023

Pre-existing frontal lobe dysfunction signs as predictors of subsequent neurotoxicity in CAR T cell therapy: insights from a case series.

Lorenzo Fontanelli, Chiara Pizzanelli, Chiara Milano, Raffaella Cassano Cassano, Sara Galimberti, Maria Ida Rossini, Ignazio Santo, Francesco Turco, Enrica Bonanni, Gabriele Siciliano and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 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

12 authors at 1 institution in 1 country.

Lorenzo Fontanelli *Department of Clinical and Experimental Medicine, Neurology Unit, University of Pisa, Pisa, Italy.
Chiara Pizzanelli *Department of Clinical and Experimental Medicine, Neurology Unit, University of Pisa, Pisa, Italy. c.pizzanelli@ao-pisa.toscana.it.ORCID http://orcid.org/0000-0001-5044-8944
Chiara MilanoDepartment of Clinical and Experimental Medicine, Neurology Unit, University of Pisa, Pisa, Italy.
Raffaella Cassano CassanoDepartment of Clinical and Experimental Medicine, Haematology Unit, University of Pisa, Pisa, Italy.
Sara GalimbertiDepartment of Clinical and Experimental Medicine, Haematology Unit, University of Pisa, Pisa, Italy.
Maria Ida RossiniDepartment of Clinical and Experimental Medicine, Haematology Unit, University of Pisa, Pisa, Italy.
Ignazio SantoDepartment of Clinical and Experimental Medicine, Haematology Unit, University of Pisa, Pisa, Italy.
Francesco TurcoDepartment of Clinical and Experimental Medicine, Neurology Unit, University of Pisa, Pisa, Italy.
Enrica BonanniDepartment of Clinical and Experimental Medicine, Neurology Unit, University of Pisa, Pisa, Italy.
Gabriele SicilianoDepartment of Clinical and Experimental Medicine, Neurology Unit, University of Pisa, Pisa, Italy.
Enrico OrciuoloDepartment of Clinical and Experimental Medicine, Haematology Unit, University of Pisa, Pisa, Italy.
Filippo BaldacciDepartment of Clinical and Experimental Medicine, Neurology Unit, University of Pisa, Pisa, Italy.
University of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChimeric Antigen Receptor (CAR) T cell therapies are innovative treatments against hematological malignancies, with increasing therapeutic indications. Despite their great efficacy, these therapies are hampered by high rates of neurotoxicity (immune effector cell-associated neurotoxicity (ICANS)). In the past few years, several risk factors have been associated with ICANS and grouped together in the attempt to build validated models able to predict neurologic complications. However, little is known about pre-existing neurologic conditions possibly related to the development of neurotoxicity. METHODS AND

resultsIn our case series, including sixteen consecutive patients treated with CAR T cells, we observed that (i) neurotoxicity only occurred in the two patients who presented subtle clinical signs of frontal lobe impairment at baseline and (ii) neurologic manifestations of ICANS consisted of language disturbances and cortical frontal myoclonus, which were both manifestations of a frontal predominant dysfunction. DISCUSSION: Based on our experience, we suggest that a pre-existing frontal lobe impairment, even if at a subclinical level, may eventually drive to ICANS, which in turn shows symptoms compatible with a frontal encephalopathy. It is remarkable that this focal neurotoxicity involved the same CNS regions that were responsible of subtle neurological signs at baseline. Future studies on larger numbers of patients are needed to confirm the possible role of baseline frontal lobe dysfunction as a predictor of ICANS, in order to enhance efforts to safely deliver CAR T cell therapy.

Indexed as

Immunotherapy, AdoptiveNeurotoxicity SyndromesFrontal LobeHumansResearchcell-associated neurotoxicityCAR T cell therapyFrontal encephalopathyImmune effector cell–associated neurotoxicity syndrome (ICANS)Neurotoxicity

Identifiers

PMID37160803
PMCPMC10170036
OpenAlexW4376121933

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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.