Evidence map›Paper›PMID 36939931›Full record

ReviewJournal of neurology2023

Dysautonomia associated with immune checkpoint inhibitors.

Toshiki Tezuka, Shinichi Okuzumi, Chiho Nakashima, Toshihiro Ide, Shungo Imai, Satoru Mitsuboshi, Yuki Kuwahara, Tsubasa Takizawa, Morinobu Seki, Naoto Minematsu and 5 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 17 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

15 authors at 4 institutions in 1 country.

Toshiki TezukaDepartment of Neurology, Keio University School of Medicine, Tokyo, Japan.
Shinichi OkuzumiDepartment of Internal Medicine, Hino Municipal Hospital, Tokyo, Japan.
Chiho NakashimaDivision of Haematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Toshihiro IdeDivision of Neurology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Shungo ImaiDivision of Drug Informatics, Faculty of Pharmacy, Keio University, Tokyo, Japan.
Satoru MitsuboshiDivision of Drug Informatics, Faculty of Pharmacy, Keio University, Tokyo, Japan.
Yuki KuwaharaDivision of Haematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Tsubasa TakizawaDepartment of Neurology, Keio University School of Medicine, Tokyo, Japan.
Morinobu SekiDepartment of Neurology, Keio University School of Medicine, Tokyo, Japan.
Naoto MinematsuDepartment of Internal Medicine, Hino Municipal Hospital, Tokyo, Japan.
Naoko AraganeDivision of Haematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Jin NakaharaDepartment of Neurology, Keio University School of Medicine, Tokyo, Japan.
Satoko HoriDivision of Drug Informatics, Faculty of Pharmacy, Keio University, Tokyo, Japan.
Shunya NakaneDepartment of Neurology, Nippon Medical University, Tokyo, Japan.
Shigeaki SuzukiDepartment of Neurology, Keio University School of Medicine, Tokyo, Japan. sgsuzuki@keio.jp.ORCID http://orcid.org/0000-0003-4388-4574
Keio University · JPSaga University · JPNagano Municipal Hospital · JPNippon Medical School · JP

Funding

Japan Society for the Promotion of Science JP20H03592
6 · The paper itself

Abstract

objectiveThe purpose of this study is to report the clinical characteristics of dysautonomia associated with immune checkpoint inhibitors (ICIs).

methodsWe reported two patients with autoimmune autonomic ganglionopathy (AAG) occurring as immune-related adverse events (irAEs). We also performed a review of previous case reports presenting dysautonomia during ICI therapy. Moreover, we conducted pharmacovigilance analyses using the US Food and Drug Administration Adverse Events Reporting System (FAERS) to investigate dysautonomia associated with ICI.

resultsTwo patients in our care developed both AAG and autoimmune encephalitis following ICI therapy for lung cancers. We comprehensively reviewed 13 published cases (M:F = 11:2, mean onset age of 53 years) with ICI-associated dysautonomia including AAG (n = 3) and autonomic neuropathy (n = 10). Of these, ICI monotherapy was performed in seven and combination ICI use in six. In 6 of 13 patients, dysautonomia appeared within one month after the start of ICIs. Orthostatic hypotension was observed in 7 and urinary incontinence or retention in five. All patients except three showed gastrointestinal symptoms. Anti-ganglionic acetylcholine receptor antibodies were undetectable. All but two patients received immune-modulating therapy. Immuno-modulating therapy was effective in three patients with AAG and two patients with autonomic neuropathy, but ineffective in the others. Five patients died, of either the neurological irAE (n = 3) or cancer (n = 2). The pharmacovigilance analyses using FAERS showed that ipilimumab monotherapy and the combination of nivolumab and ipilimumab constituted significant risks for developing dysautonomia, consistent with the review of literature.

conclusionICIs can cause dysautonomia including AAG, and autonomic neuropathy is a neurological irAE.

Indexed as

Autoimmune DiseasesLung NeoplasmsNervous System DiseasesPrimary DysautonomiasAutoantibodiesHumansImmune Checkpoint InhibitorsIpilimumabMiddle AgedNivolumabAutoantibodiesImmune Checkpoint InhibitorsIpilimumabNivolumabAutoimmune autonomic ganglionopathyDysautonomiaImmune-related adverse eventsPharmacovigilanceReview of literature

Identifiers

PMID36939931
OpenAlexW4327896639

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.