Evidence map›Paper›PMID 39343612›Full record

ArticleJournal of clinical and experimental hematopathology : JCEH2024

Salivary gland swelling as a characteristic manifestation of local cytokine release syndrome after anti-CD19 chimeric antigen receptor T cell therapy: A case series.

Saki Kawase, Masatoshi Sakurai, Kyoko Masuda, Yusuke Kubota, Takahide Shindo, Ami Inokuchi, Hiroyoshi Hayashi, Misa Nakayasu, Yuka Shiozawa, Tomohiro Hirai and 6 more

Abstract readCase Reports
In one paragraph

Article in Journal of clinical and experimental hematopathology : JCEH, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

16 authors.

Saki KawaseDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Masatoshi SakuraiDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Kyoko MasudaDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Yusuke KubotaDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Takahide ShindoDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Ami InokuchiDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Hiroyoshi HayashiDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Misa NakayasuDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Yuka ShiozawaDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Tomohiro HiraiDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Takahiro InoueDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Takayuki FujiiDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Haryoon KimDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Yuya KodaDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Jun KatoDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Keisuke KataokaDivision of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytokine release syndrome (CRS) is the most common adverse event of chimeric antigen receptor T (CAR-T) cell therapy and is usually characterized by systemic symptoms such as fever, hypotension, and hypoxia. However, there have been several recent reports of local CRS characterized by cervical swelling. This localized syndrome can cause life-threatening laryngeal edema and requires early diagnostic treatment. Here we report 3 cases of local CRS where bilateral salivary gland swelling emerged following anti-CD19 CAR-T cell therapy for relapsed or refractory diffuse large B-cell lymphoma. Following tocilizumab treatment for systemic CRS, all patients exhibited cervical swelling. Physical examinations revealed significant swelling of the bilateral submandibular glands, and computed tomography scans showed substantial enlargement of the bilateral parotid and submandibular glands. Immediate treatment with dexamethasone effectively managed the potentially life-threatening laryngeal or pharyngeal edema, thereby preventing severe airway obstruction. This study has demonstrated, for the first time to our knowledge, that salivary gland enlargement is a common finding in local CRS. This observation suggests that physicians should continue to closely monitor the risk of developing cervical edema leading to life-threatening airway obstruction after systemic CRS, even in patients treated with tocilizumab. If salivary gland swelling is observed, it would be better to consider prompt evaluation and dexamethasone administration.

Indexed as

Cytokine Release SyndromeAdultAgedAntibodies, Monoclonal, HumanizedAntigens, CD19DexamethasoneEdemaFemaleHumansImmunotherapy, AdoptiveLymphoma, Large B-Cell, DiffuseMaleMiddle AgedSalivary GlandsAntibodies, Monoclonal, HumanizedAntigens, CD19Dexamethasonetocilizumabchimeric antigen receptor T cell therapycytokine release syndromedexamethasonemalignant lymphomasalivary gland

Identifiers

PMID39343612
PMCPMC11528259

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Registered trials

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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.