Evidence map›Paper›PMID 32388608›Full record

ReviewAnnals of hematology2020

Chimeric antigen receptor therapy in hematological malignancies: antigenic targets and their clinical research progress.

Juanjuan Zhao, Meirong Wu, Zhifeng Li, Sheng Su, Yin Wen, Litian Zhang, Yuhua Li

Abstract readReview
PubMed Publisher
In one paragraph

Review in Annals of hematology, 2020. 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
0.3field-weighted citation impact, top 40% 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, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. The role of DNA mismatch repair in immunotherapy of human cancer.International journal of biological sciences · 2022
    Review
  8. 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

7 authors at 3 institutions in 1 country.

Juanjuan ZhaoDepartment of Hematology, Zhujiang Hospital, Southern Medical University, No. 253, Middle Gongye Avenue, Guangzhou, 510282, Guangdong, People's Republic of China.
Meirong WuDepartment of Hematology, Zhujiang Hospital, Southern Medical University, No. 253, Middle Gongye Avenue, Guangzhou, 510282, Guangdong, People's Republic of China.
Zhifeng LiDepartment of Hematology, Zhujiang Hospital, Southern Medical University, No. 253, Middle Gongye Avenue, Guangzhou, 510282, Guangdong, People's Republic of China.
Sheng SuDepartment of Hematology, Zhujiang Hospital, Southern Medical University, No. 253, Middle Gongye Avenue, Guangzhou, 510282, Guangdong, People's Republic of China.
Yin WenDepartment of Hematology, Zhujiang Hospital, Southern Medical University, No. 253, Middle Gongye Avenue, Guangzhou, 510282, Guangdong, People's Republic of China.
Litian ZhangDepartment of Hematology, Zhujiang Hospital, Southern Medical University, No. 253, Middle Gongye Avenue, Guangzhou, 510282, Guangdong, People's Republic of China.
Yuhua LiDepartment of Hematology, Zhujiang Hospital, Southern Medical University, No. 253, Middle Gongye Avenue, Guangzhou, 510282, Guangdong, People's Republic of China. liyuhua2011gz@163.com.
Zhujiang Hospital · CNSouthern Medical University · CNGuangzhou Regenerative Medicine and Health Guangdong Laboratory · CN

Funding

Frontier Research Program of Guangzhou Regenerative Medicine and Health Guangdong Laboratory (CN) 2018GZR110105014Natural Science Foundation of Guangdong Province (CN) 2018B030311042Science and Technology Program of Guangzhou (CN) 201704020216
6 · The paper itself

Abstract

Chimeric antigen receptor (CAR)-based immunotherapy has achieved dramatic success in the treatment of B cell malignancies, based on the summary of current research data, and has shown good potential in early phase cancer clinical trials. Modified constructs are being optimized to recognize and destroy tumor cells more effectively. By targeting the proper B-lineage-specific antigens such as CD19 and CD20, adoptive immunotherapy has demonstrated promising clinical results and already plays a role in the treatment of several lymphoid malignancies, which highlights the importance of target selection for other CAR therapies. The high efficacy of CAR-T cells has resulted in the approval of anti-CD19-directed CAR-T cells for the treatment of B cell malignancies. In this review, we focus on the basic structure and current clinical application of CAR-T cells, detail the research progress of CAR-T for different antigenic targets in hematological malignancies, and further discuss the current barriers and proposed solutions, investigating the possible mechanisms of recurrence of CAR-T cell therapy. A summary of the paper is also given to overview as the prospects for this therapy.

Indexed as

Hematologic NeoplasmsImmunotherapy, AdoptiveAntigens, CD19Antigens, CD20Antigens, NeoplasmHumansReceptors, Chimeric AntigenAntigens, CD19Antigens, CD20Antigens, NeoplasmReceptors, Chimeric AntigenAdoptive cell therapyChimeric antigen receptorClinical efficacyHematological malignanciesRecurrenceTargeted therapy

Identifiers

PMID32388608
OpenAlexW3022593326

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.