Evidence map›Paper›PMID 33515299›Full record

ArticleJournal of neurology2021

Immune checkpoint inhibitors for progressive multifocal leukoencephalopathy: a new gold standard?

Damien Roos-Weil, Nicolas Weiss, Amélie Guihot, Madalina Uzunov, Agnès Bellanger, Bruno Eymard, David Saadoun, Caroline Houillier, Ahmed Idbaih, Sophie Demeret and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

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  14. Clinical outcomes after use of checkpoint inhibitor immunotherapies in people with multiple sclerosis.Multiple sclerosis journal - experimental, translational and clinical
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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

15 authors at 3 institutions in 1 country.

Damien Roos-Weil *Sorbonne Université, Service d'Hématologie Clinique, Hôpital Pitié-Salpêtrière, APHP, 47-83 Bd de l'Hôpital, 75651, Paris Cedex, France. damien.roosweil@aphp.fr.ORCID http://orcid.org/0000-0002-7767-755X
Nicolas Weiss *Sorbonne Université, AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Neurologie, Unité de Médecine Intensive Réanimation Neurologique, and Institut du Cerveau et de la Moelle Épinière, ICM, F-75013, Paris, France.
Amélie GuihotSorbonne UniversitéAssistance Publique-Hôpitaux de Paris (AP-HP), Groupe Hospitalier Pitié-SalpêtrièreInserm U1135, CNRS ERL 8255, Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), Département d'Immunologie, Paris, France.
Madalina UzunovSorbonne Université, Service d'Hématologie Clinique, Hôpital Pitié-Salpêtrière, APHP, 47-83 Bd de l'Hôpital, 75651, Paris Cedex, France.
Agnès BellangerPharmacie à Usage Intérieur, Sorbonne Université, AP-HP, Hôpital Pitié-Salpêtrière, APHP, Paris, France.
Bruno EymardNord-Est/Ile-de-France Neuromuscular Reference Center, Myology Institute, Pitié-Salpêtrière Hospital, Paris, France.
David SaadounDepartment of Internal Medicine and Clinical Immunology, Centre National de Références Maladies Autoimmunes Systémiques Rares, Centre National de Références Maladies Autoinflammatoires Rares et Amyloses Inflammatoires, Sorbonne Université, AP-HP, Hôpital Pitié-Salpêtrière, Paris, France.
Caroline HouillierCNRS, UMR S 1127, Institut du Cerveau et de la Moelle Épinière, ICM, Sorbonne Université, Inserm, AP-HPHôpitaux Universitaires la Pitié Salpêtrière, Charles Foix, Service de Neurologie 2-Mazarin, F-75013, Paris, France.
Ahmed IdbaihCNRS, UMR S 1127, Institut du Cerveau et de la Moelle Épinière, ICM, Sorbonne Université, Inserm, AP-HPHôpitaux Universitaires la Pitié Salpêtrière, Charles Foix, Service de Neurologie 2-Mazarin, F-75013, Paris, France.
Sophie DemeretSorbonne Université, AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Neurologie, Unité de Médecine Intensive Réanimation Neurologique, and Institut du Cerveau et de la Moelle Épinière, ICM, F-75013, Paris, France.
Claire DebackLaboratoire de Virologie, AP-HP, Hôpitaux Universitaires Paris Sud Saclay, Hôpital Paul Brousse, Villejuif, France.
Véronique LeblondSorbonne Université, Service d'Hématologie Clinique, Hôpital Pitié-Salpêtrière, APHP, 47-83 Bd de l'Hôpital, 75651, Paris Cedex, France.
Damien GalanaudDepartment of Neuroradiology, Sorbonne Université, Pitié Salpêtrière Hospital, APHP, Paris, France.
Natalia ShorDepartment of Neuroradiology, Sorbonne Université, Pitié Salpêtrière Hospital, APHP, Paris, France.
Valérie PourcherSorbonne Université, AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière Charles Foix, Institut Pierre Louis d'Épidémiologie et de Santé Publique, Service de Maladies Infectieuses et Tropicales, INSERM 1136, 47-83 Bd de l'Hôpital, 75651, Paris Cedex, France. valerie.martinez@aphp.fr.
Sorbonne Université · FRCentre National de la Recherche Scientifique · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesProgressive multifocal leukoencephalopathy (PML) is a very rare and opportunistic encephalitis caused by JC polyomavirus that is linked to profound immunosuppression and is usually fatal unless immune function can be restored. Immune checkpoint inhibitors (ICI) are monoclonal antibodies (mAbs) that block either CTLA-4 or PD-1 inhibitor receptors, thus enhancing antiviral T-cell activity. Successful treatment of PML by ICI has recently generated some enthusiasm in case reports/small series of patients. However, the initial enthusiasm was mitigated by some individual case reports that did not show any benefit. More data are thus warranted about efficacy of immune checkpoint inhibitors in the specific context of PML. METHODS AND

resultsWe report here the outcomes of six PML patients treated by ICI between 2017 and 2019. Underlying causes of immunosuppression consisted in hematologic malignancies (n = 4), primary immune deficiency (n = 1) and use of immunosuppressive therapies for myasthenia gravis (n = 1). Three patients were alive with a mean follow-up of 21 months (14-33) after first ICI infusion, including one patient with frank clinical response, one with stabilization, and one with initial worsening and further stabilization of PML. The three other patients rapidly died from PML.

conclusionsOur data suggest that ICI may be effective for PML treatment but were less impressive than the ones previously reported. Larger studies are thus warranted to confirm this efficacy and to identify the predictive factors of response.

Indexed as

Antineoplastic Agents, ImmunologicalJC VirusLeukoencephalopathy, Progressive MultifocalAntibodies, MonoclonalHumansImmune Checkpoint InhibitorsAntibodies, MonoclonalAntineoplastic Agents, ImmunologicalImmune Checkpoint InhibitorsImmune checkpoint inhibitorImmunosuppressionJCVPD-1Progressive multifocal leukoencephalopathy

Identifiers

PMID33515299
OpenAlexW3124154059

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.