Evidence map›Paper›PMID 38006053›Full record

ReviewVaccines2023

CAR-T-Cell Therapy in Multiple Myeloma: B-Cell Maturation Antigen (BCMA) and Beyond.

Abhinava K Mishra, Ashna Gupta, Gunjan Dagar, Dayasagar Das, Abhijit Chakraborty, Shabirul Haque, Chandra Prakash Prasad, Archana Singh, Ajaz A Bhat, Muzafar A Macha and 10 more

Open access · goldAbstract readReview
In one paragraph

Review in Vaccines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
8.7field-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

29 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
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  11. Targets for CAR Therapy in Multiple Myeloma.International journal of molecular sciences · 2025
    Review
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  15. Article
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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

20 authors at 10 institutions in 3 countries.

Abhinava K MishraMolecular, Cellular and Developmental Biology Department, University of California Santa Barbara, Santa Barbara, CA 93106, USA.ORCID 0000-0003-3733-3928
Ashna GuptaDepartment of Medical Oncology (Lab), Dr. BRAIRCH, All India Institute of Medical Sciences (AIIMS), New Delhi 110029, India.
Gunjan DagarDepartment of Medical Oncology (Lab), Dr. BRAIRCH, All India Institute of Medical Sciences (AIIMS), New Delhi 110029, India.
Dayasagar DasDepartment of Medicine, NYU Langone Health, New York, NY 10016, USA.
Abhijit ChakrabortyDepartment of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.ORCID 0000-0002-3822-5657
Shabirul HaqueFeinstein Institute of Medical Research, Northwell Health, Manhasset, NY 11030, USA.ORCID 0000-0002-6721-0630
Chandra Prakash PrasadDepartment of Medical Oncology (Lab), Dr. BRAIRCH, All India Institute of Medical Sciences (AIIMS), New Delhi 110029, India.ORCID 0000-0002-4911-7483
Archana SinghDepartment of Biochemistry, All India Institute of Medical Sciences (AIIMS), New Delhi 110029, India.
Ajaz A BhatPrecision Medicine in Diabetes, Obesity and Cancer Program, Department of Human Genetics, Sidra Medicine, Doha P.O. Box 26999, Qatar.ORCID 0000-0003-3640-6275
Muzafar A MachaWatson-Crick Centre for Molecular Medicine, Islamic University of Science and Technology, Awantipora 192122, India.ORCID 0000-0003-4468-4435
Moez BenaliFortrea Inc., Durham, NC 27709, USA.
Kamal S SainiFortrea Inc., Durham, NC 27709, USA.ORCID 0000-0001-6301-3309
Rebecca Ann PrevisLabcorp Oncology, Durham, NC 27560, USA.ORCID 0000-0001-8087-9120
Deepak SainiDepartment of Materia Medica, State Lal Bahadur Shastri Homoeopathic Medical College, Prayagraj 211013, India.ORCID 0000-0002-3552-7932
Dwaipayan SahaPratap Chandra Memorial Homoeopathic Hospital & College, Kolkata 700011, India.ORCID 0009-0007-7262-2289
Preyangsee DuttaPratap Chandra Memorial Homoeopathic Hospital & College, Kolkata 700011, India.ORCID 0009-0003-8380-1822
Aseem Rai BhatnagarDepartment of Radiation Oncology, Henry Ford Cancer Institute, Detroit, MI 48202, USA.
Mrinalini DarswalHarvard T.H. Chan School of Public Health, Huntington Ave, Boston, MA 02115, USA.
Abhishek ShankarDepartment of Radiation Oncology, Dr. BRAIRCH, All India Institute of Medical Sciences (AIIMS), New Delhi 110029, India.ORCID 0000-0001-6491-0079
Mayank SinghDepartment of Medical Oncology (Lab), Dr. BRAIRCH, All India Institute of Medical Sciences (AIIMS), New Delhi 110029, India.ORCID 0000-0003-0728-1936
All India Institute of Medical Sciences · INSwami Pranavananda Homoeopathic Medical College and Hospital · INCambridge University Hospitals NHS Foundation Trust · GBDuke Medical Center · USHarvard University · USIslamic University of Science and Technology · INNorthwell Health · USNYU Langone Health · USThe University of Texas MD Anderson Cancer Center · USUniversity of California, Santa Barbara · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Significant progress has been achieved in the realm of therapeutic interventions for multiple myeloma (MM), leading to transformative shifts in its clinical management. While conventional modalities such as surgery, radiotherapy, and chemotherapy have improved the clinical outcomes, the overarching challenge of effecting a comprehensive cure for patients afflicted with relapsed and refractory MM (RRMM) endures. Notably, adoptive cellular therapy, especially chimeric antigen receptor T-cell (CAR-T) therapy, has exhibited efficacy in patients with refractory or resistant B-cell malignancies and is now also being tested in patients with MM. Within this context, the B-cell maturation antigen (BCMA) has emerged as a promising candidate for CAR-T-cell antigen targeting in MM. Alternative targets include SLAMF7, CD38, CD19, the signaling lymphocyte activation molecule CS1, NKG2D, and CD138. Numerous clinical studies have demonstrated the clinical efficacy of these CAR-T-cell therapies, although longitudinal follow-up reveals some degree of antigenic escape. The widespread implementation of CAR-T-cell therapy is encumbered by several barriers, including antigenic evasion, uneven intratumoral infiltration in solid cancers, cytokine release syndrome, neurotoxicity, logistical implementation, and financial burden. This article provides an overview of CAR-T-cell therapy in MM and the utilization of BCMA as the target antigen, as well as an overview of other potential target moieties.

Indexed as

B-cell maturation antigen (BCMA)CAR-T-cell therapymultiple myeloma (MM)

Identifiers

PMID38006053
PMCPMC10674477
OpenAlexW4388722936

What OpenQuestion holds

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Registered trials

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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.