Evidence map›Paper›PMID 37754488›Full record

ReviewCurrent oncology (Toronto, Ont.)2023

SLAMF7 as a Promising Immunotherapeutic Target in Multiple Myeloma Treatments.

Emily Chu, Jian Wu, Stacey S Kang, Yubin Kang

Open access · goldAbstract readReview
In one paragraph

Review in Current oncology (Toronto, Ont.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
9.9field-weighted citation impact, top 2% 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

25 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  4. Review
  5. Review
  6. DNA methylation profiling of human CD4Immunology and cell biology · 2026
    Article
  7. Review
  8. Review
  9. Targets for CAR Therapy in Multiple Myeloma.International journal of molecular sciences · 2025
    Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Myeloid cells meet CD8Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2024
    Article
  18. Article
  19. Review
  20. Are we there yet? CAR-T therapy in multiple myeloma.British journal of haematology · 2024
    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

4 authors at 3 institutions in 1 country.

Emily ChuDivision of Hematologic Malignancies and Cellular Therapy, Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA.
Jian WuDivision of Hematologic Malignancies and Cellular Therapy, Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA.ORCID 0000-0001-7065-9917
Stacey S KangCollege of Arts and Sciences, Washington University in St. Louis, St. Louis, MO 63130, USA.
Yubin KangDivision of Hematologic Malignancies and Cellular Therapy, Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA.
Duke Medical Center · USDuke University · USWashington University in St. Louis · US

Funding

Clinical Trial of ABC294640 in Patients with Refractory Multiple MyelomaR44CA199767 · NCI · APOGEE BIOTECHNOLOGY CORPORATION · PI SMITH, CHARLES D · 2015 to 2017
$2.0M
Targeting sphingosine kinase 2 for the treatment of multiple myelomaR01CA197792 · NCI · DUKE UNIVERSITY · PI KANG, YUBIN · 2015 to 2019
$1.8M
Thioredoxin, a novel agent for mitigating radiation-induced hematopoietic injuryR56HL155582 · NHLBI · DUKE UNIVERSITY · PI KANG, YUBIN · 2022 to 2022
$443k
Role of SLAMF7 in Racial Disparities in MyelomaR21CA280499 · NCI · DUKE UNIVERSITY · PI KANG, YUBIN · 2023 to 2024
$414k
Enhancing CAR T therapy in multiple myelomaR21CA267275 · NCI · DUKE UNIVERSITY · PI KANG, YUBIN · 2022 to 2023
$410k
Effects of PPAR agonists on response to immunomodulatory agents in patients with multiple myelomaR21CA234701 · NCI · DUKE UNIVERSITY · PI KANG, YUBIN · 2019 to 2020
$385k
NCI NIH HHS R01 CA197792NCI NIH HHS R01CA197792NCI NIH HHS R21 CA234701NCI NIH HHS R21CA234701NCI NIH HHS R21 CA267275NCI NIH HHS R21 CA280499NCI NIH HHS R44 CA199767NCI NIH HHS R44CA199767NCI NIH HHS R56HL155582NHLBI NIH HHS R56 HL155582
6 · The paper itself

Abstract

Multiple myeloma (MM) is a common hematological malignancy that has fostered several new therapeutic approaches to combat newly diagnosed or relapsed MM. While the field has advanced over the past 2 decades, the majority of patients will develop resistance to these treatments, causing the need for new therapeutic targets. SLAMF7 is an attractive therapeutic target in multiple myeloma, and a monoclonal antibody that targets SLAMF7 has shown consistent beneficial outcomes in clinical trials to date. In this review, we will focus on the structure and regulation of SLAMF7 and its mechanism of action. The most recent clinical trials will be reviewed to further understand the clinical implications and improve the prognosis of MM. Furthermore, the efficacy of anti-SLAMF7 monoclonal antibodies combined with standard therapies and possible resistance mechanisms will be discussed. This review aimed to provide a detailed summary of the role of SLAMF7 in the pathogenesis of patients with MM and the rationale for further investigation into SLAMF7-mediated molecular pathways associated with MM development.

Indexed as

Antineoplastic AgentsMultiple MyelomaAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedHumansImmunotherapySignaling Lymphocytic Activation Molecule FamilyAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic AgentsSignaling Lymphocytic Activation Molecule FamilySLAMF7 protein, humanantibody-based immunotherapyCAR-Telotuzumabmultiple myelomaSLAMF7

Identifiers

PMID37754488
PMCPMC10529721
OpenAlexW4386219363

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.