Evidence map›Paper›PMID 39891674›Full record

ReviewCancer immunology, immunotherapy : CII2025

Targeting BCMA in multiple myeloma: designs, challenges, and future directions.

Yi Hu, Yuetao Xie, Xiaodong Wang, Lufeng Yang, He Geng, Zugang Yi, Yao Zhang, Lin Ma, Fang Chen

Abstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2025. 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
–field-weighted citation impact
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.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Targets for CAR Therapy in Multiple Myeloma.International journal of molecular sciences · 2025
    Review
  8. Article
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

9 authors.

Yi HuDepartment of Anesthesiology, Shenzhen Children's Hospital, Shenzhen, 518038, Guangdong, China.
Yuetao XieDepartment of Anesthesiology, Shenzhen Children's Hospital, Shenzhen, 518038, Guangdong, China.
Xiaodong WangDepartment of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen, 518038, Guangdong, China.
Lufeng YangDepartment of Anesthesiology, Shenzhen Children's Hospital, Shenzhen, 518038, Guangdong, China.
He GengDepartment of Anesthesiology, Shenzhen Children's Hospital, Shenzhen, 518038, Guangdong, China.
Zugang YiDepartment of Anesthesiology, Shenzhen Children's Hospital, Shenzhen, 518038, Guangdong, China.
Yao ZhangDepartment of Anesthesiology, Shenzhen Children's Hospital, Shenzhen, 518038, Guangdong, China.
Lin MaDepartment of Anesthesiology, Shenzhen Children's Hospital, Shenzhen, 518038, Guangdong, China.
Fang ChenDepartment of Anesthesiology, Shenzhen Children's Hospital, Shenzhen, 518038, Guangdong, China. fangchen18938690929@gmail.com.

Funding

Natural Science Foundation of Shenzhen Science and Technology Innovation Commission JCY20220530155613030
6 · The paper itself

Abstract

Chimeric antigen receptor (CAR) T cell therapy has emerged as a groundbreaking immunotherapy, demonstrating significant efficacy in treating B cell malignancies. In the context of multiple myeloma (MM), B cell maturation antigen (BCMA) has been identified as a critical target, driving the development of CAR T cell therapies designed to address this plasma cell cancer. Various CAR designs, utilizing different BCMA recognition domains, have yielded promising clinical results, leading to the approval of two BCMA-targeting CAR T cell therapies by the US Food and Drug Administration (FDA) for the treatment of MM. This review uniquely examines the BCMA CAR T cell landscape, emphasizing the design of recognition domains, clinical efficacy, and patient outcomes. It critically addresses emerging challenges such as antigen escape and toxicity profiles, which have surfaced alongside therapeutic advances. Moreover, the review spotlights cutting-edge developments, including dual-targeting CAR T strategies, advancements in CAR T cell manufacturing, and innovative allogeneic CAR T approaches utilizing healthy donor cells. By detailing both the breakthroughs and ongoing challenges in BCMA CAR T cell therapy, this review offers a comprehensive perspective on the current state and future possibilities of CAR T cell therapy for MM and its expanding role in treating hematologic malignancies and beyond.

Indexed as

B-Cell Maturation AntigenImmunotherapy, AdoptiveMultiple MyelomaReceptors, Chimeric AntigenAnimalsHumansB-Cell Maturation AntigenReceptors, Chimeric AntigenTNFRSF17 protein, humanB cell maturation antigenChimeric antigen receptorImmunotherapyMultiple myelomaT cells

Identifiers

PMID39891674
PMCPMC11787132

What OpenQuestion holds

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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.