Evidence map›Paper›PMID 31798590›Full record

ReviewFrontiers in immunology2019

Mechanisms of Relapse After CD19 CAR T-Cell Therapy for Acute Lymphoblastic Leukemia and Its Prevention and Treatment Strategies.

Xinjie Xu, Qihang Sun, Xiaoqian Liang, Zitong Chen, Xiaoli Zhang, Xuan Zhou, Meifang Li, Huilin Tu, Yu Liu, Sanfang Tu and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 209 papers.

0numbers the graph read from it
0cells of the map it votes in
209citing papers in PubMed
15.6field-weighted citation impact, top 1% 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

209 citing papers in PubMed, 329 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. CD22 as a Target for Hematological Malignancies and Autoimmune Diseases.International journal of molecular sciences · 2026
    Review
  8. Review
  9. Review
  10. Review
  11. Adoptive T-cell therapies in the clinic.Bioengineering & translational medicine · 2026
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review

149 more citing papers are in PubMed but not listed here.

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

11 authors at 2 institutions in 1 country.

Xinjie XuDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Qihang SunDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Xiaoqian LiangDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Zitong ChenDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Xiaoli ZhangDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Xuan ZhouDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Meifang LiDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Huilin TuDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Yu LiuDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Sanfang TuDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Yuhua LiDepartment of Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Zhujiang Hospital · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor (CAR) T-cell therapy is highly effective in the treatment of B-cell acute lymphoblastic leukemia (ALL) or B-cell lymphoma, providing alternative therapeutic options for patients who failed to respond to conventional treatment or relapse. Moreover, it can bridge other therapeutic strategies and greatly improve patient prognosis, with broad applicable prospects. Even so, 30-60% patients relapse after treatment, probably due to persistence of CAR T-cells and escape or downregulation of CD19 antigen, which is a great challenge for disease control. Therefore, understanding the mechanisms that underlie post-CAR relapse and establishing corresponding prevention and treatment strategies is important. Herein, we discuss post-CAR relapse from the aspects of CD19-positive and CD19-negative and provide some reasonable prevention and treatment strategies.

Indexed as

Antigens, CD19HumansImmunotherapy, AdoptiveNeoplasm Recurrence, LocalPrecursor Cell Lymphoblastic Leukemia-LymphomaReceptors, Chimeric AntigenAntigens, CD19CD19 molecule, humanReceptors, Chimeric AntigenCD19 CAR T-cellmechanismspreventionrelapsestrategiestreatment

Identifiers

PMID31798590
PMCPMC6863137
OpenAlexW2988100850

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.