Evidence map›Paper›PMID 31802905›Full record

ArticleOncoTargets and therapy2019

Coexistence Of A Huge Venous Thromboembolism And Bleeding Tendency In Cytokine Release Syndrome During CAR-T Therapy.

Haiyan Liu, Ye Yang, Jie Jiang, Xinfeng Wang, Chenlu Zhang, Yijing Jiang, Lemin Hong, Hongming Huang

Open access · goldAbstract readCase Reports
In one paragraph

Article in OncoTargets and therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. COVID-19-Associated Coagulopathy: An Exacerbated Immunothrombosis Response.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    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

8 authors at 2 institutions in 1 country.

Haiyan Liu *Department of Hematology, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, People's Republic of China.
Ye Yang *School of Integrative Medicine, Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210023, People's Republic of China.ORCID 0000-0003-0228-5102
Jie JiangDepartment of Hematology, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, People's Republic of China.
Xinfeng WangDepartment of Hematology, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, People's Republic of China.
Chenlu ZhangDepartment of Hematology, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, People's Republic of China.
Yijing JiangDepartment of Hematology, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, People's Republic of China.
Lemin HongDepartment of Hematology, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, People's Republic of China.ORCID 0000-0003-0530-1622
Hongming HuangDepartment of Hematology, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, People's Republic of China.ORCID 0000-0001-9695-4674
Nantong University · CNNanjing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor (CAR)-modified T cell therapy is increasingly administered for hematological malignancies. Cytokine release syndrome (CRS) is a common and severe complication of CAR-T therapy. In the present case, a 62-year-old male patient was diagnosed with relapsed and refractory multiple myeloma (RRMM). Treated with CART-CD19/BCMA therapy, his symptoms remitted, during which occasional but severe CRS associated with coagulation disorder still appeared, as evidenced by the coexistence of a huge thrombosis and bleeding tendency. Through the First Generation Sequencing, we extracted genomic DNA from the patient's peripheral blood to analyze the distribution of polymorphism at the -572C/G site of the promoter of IL-6 gene. The results showed that the genotype of -572C/G promoter polymorphism was CC, indicating that high level of IL-6 and -572C/G polymorphism might be associated with the risk of thrombotic disorders. We concluded that immediate diagnosis and appropriate treatment of coagulopathy could reduce CRS-related mortality.

Indexed as

chimeric antigen receptor-T therapycoagulation disordercytokine release syndromemultiple myelomathrombosis

Identifiers

PMID31802905
PMCPMC6826178
OpenAlexW2982445524

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.