Evidence map›Paper›PMID 36701037›Full record

ReviewCurrent treatment options in oncology2023

Small-Molecule Compounds Boost CAR-T Cell Therapy in Hematological Malignancies.

Xinping Cao, Xin Jin, Xiaomei Zhang, Paudel Utsav, Yi Zhang, Ruiting Guo, Wenyi Lu, Mingfeng Zhao

Open access · hybridAbstract readReview
In one paragraph

Review in Current treatment options in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  6. Modulation of anti-tumour immunity by XPO1 inhibitors.Exploration of targeted anti-tumor therapy · 2025
    Review
  7. Relapsed/refractory CLL: the role of allo-SCT, CAR-T, and T-cell engagers.Hematology. American Society of Hematology. Education Program · 2024
    Review
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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 3 institutions in 1 country.

Xinping CaoFirst Center Clinic College of Tianjin Medical University, Tianjin, 300192, China.
Xin JinDepartment of Hematology, Tianjin First Central Hospital, Tianjin, 300192, China.
Xiaomei ZhangSchool of Medicine, Nankai University, Tianjin, 300071, China.
Paudel UtsavFirst Center Clinic College of Tianjin Medical University, Tianjin, 300192, China.
Yi ZhangFirst Center Clinic College of Tianjin Medical University, Tianjin, 300192, China.
Ruiting GuoFirst Center Clinic College of Tianjin Medical University, Tianjin, 300192, China.
Wenyi LuDepartment of Hematology, Tianjin First Central Hospital, Tianjin, 300192, China. luwenyi0323@163.com.
Mingfeng ZhaoDepartment of Hematology, Tianjin First Central Hospital, Tianjin, 300192, China. mingfengzhao@sina.com.ORCID 0000-0002-5995-7558
Tianjin Medical University · CNTianjin First Center Hospital · CNNankai University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

opinion statementAlthough chimeric antigen receptor T cell immunotherapy has been successfully applied in patients with hematological malignancies, several obstacles still need to be overcome, such as high relapse rates and side effects. Overcoming the limitations of CAR-T cell therapy and boosting the efficacy of CAR-T cell therapy are urgent issues that must be addressed. The exploration of small-molecule compounds in combination with CAR-T cell therapies has achieved promising success in pre-clinical and clinical studies in recent years. Protein kinase inhibitors, demethylating drugs, HDAC inhibitors, PI3K inhibitors, immunomodulatory drugs, Akt inhibitors, mTOR inhibitors, and Bcl-2 inhibitors exhibited potential synergy in combination with CAR-T cell therapy. In this review, we will discuss the recent application of these combination therapies for improved outcomes of CAR-T cell therapy.

Indexed as

Hematologic NeoplasmsReceptors, Chimeric AntigenCell- and Tissue-Based TherapyHumansImmunotherapy, AdoptivePhosphatidylinositol 3-KinasesProtein Kinase InhibitorsPhosphatidylinositol 3-KinasesProtein Kinase InhibitorsReceptors, Chimeric AntigenChimeric antigen receptor T cellsHematological malignanciesSmall-molecule compounds

Identifiers

PMID36701037
PMCPMC9992085
OpenAlexW4318049719

What Socratic 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 Socratic graph.