Evidence map›Paper›PMID 33314568›Full record

Trial reportJournal of cellular and molecular medicine2021

Ruxolitinib mitigates steroid-refractory CRS during CAR T therapy.

Jing Pan, Biping Deng, Zhuojun Ling, Weiliang Song, Jinlong Xu, Jiajia Duan, Zelin Wang, Alex H Chang, Xiaoming Feng, Yue Tan

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.3field-weighted citation impact, top 6% 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

52 citing papers in PubMed, 86 citations in OpenAlex.

  1. Ruxolitinib mitigates steroid-refractory CRS during CAR T therapy.Journal of cellular and molecular medicine · 2021
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  14. Novel strategies to manage CAR-T cell toxicity.Nature reviews. Drug discovery · 2025
    Review
  15. Article
  16. Article
  17. Article
  18. Accelerating CAR-T Cell Therapies with Small-Molecule Inhibitors.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  19. Review
  20. Review
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

10 authors at 4 institutions in 1 country.

Jing PanState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.ORCID 0000-0002-8785-0336
Biping DengCytology Laboratory, Beijing Boren Hospital, Beijing, China.
Zhuojun LingDepartment of Hematology, Beijing Boren Hospital, Beijing, China.
Weiliang SongDepartment of Hematology, Beijing Boren Hospital, Beijing, China.
Jinlong XuDepartment of Hematology, Beijing Boren Hospital, Beijing, China.
Jiajia DuanDepartment of Hematology, Beijing Boren Hospital, Beijing, China.
Zelin WangDepartment of Hematology, Beijing Boren Hospital, Beijing, China.
Alex H ChangClinical Translational Research Center, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Xiaoming FengState Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Yue TanState Key Laboratory of Experimental Hematology, Department of Hematology, Beijing Boren Hospital, Beijing, China.
Beijing Tongren Hospital · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNFujian Medical University · CNTongji University · CN

Funding

the CAMS Innovation Fund for Medical Sciences 2016-I2M-1-003the National  Key R&D Program of China 2019YFA0110200the Tianjin Science Funds for Distinguished Young Scholars 17JCJQJC45800
6 · The paper itself

Abstract

Cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity are two major CAR T related toxicities. With the interventions of Tocilizumab and steroids, many patients can recover from severe CRS. However, some patients are refractory to steroids and develop life-threatening consequences. Ruxolitinib is an oral JAKs inhibitor and promising drug in inflammatory diseases. In this pilot study, we evaluate the efficacy of Ruxolitinib in CRS. Of 14 r/r B-ALL children who received CD19 or CD22 CAR T cell therapies, 4 patients developed severe (≥grade 3) CRS with symptoms that were not alleviated with high-dose steroids and thus received ruxolitinib. Rapid resolution of CRS symptoms was observed in 4 patients after ruxolitinib treatment. Serum cytokines significantly decreased after ruxolitinib intervention. All patients achieved complete remission on day 30 after infusion, and we could still detect CAR T expansion in vivo despite usage of ruxolitinib. There were no obvious adverse events related to ruxolitinib. In vitro assays revealed that ruxolitinib could dampen CAR T expansion and cytotoxicity, suggesting that the timing and dosage of ruxolitinib should be carefully considered to avoid dampening anti-leukaemia response. Our results suggest that ruxolitinib is active and well tolerated in steroid-refractory and even life-threatening CRS.

Indexed as

AdolescentCell ProliferationChildChild, PreschoolCytokine Release SyndromeCytokinesDexamethasoneFemaleHumansImmunotherapy, AdoptiveMaleNitrilesPilot ProjectsPyrazolesPyrimidinesSteroidsCytokinesDexamethasoneNitrilesPyrazolesPyrimidinesruxolitinibSteroidsacute lymphoblastic leukemiaCAR T cell therapyhematologyimmunologyruxolitinib

Identifiers

PMID33314568
PMCPMC7812291
OpenAlexW3111280053

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.