Evidence map›Paper›PMID 36874402›Full record

ArticleCancer research communications2022

Allogeneic Anti-BCMA CAR T Cells Are Superior to Multiple Myeloma-derived CAR T Cells in Preclinical Studies and May Be Combined with Gamma Secretase Inhibitors.

Ana M Metelo, Agnieszka Jozwik, Le Anh Luong, Delaney Dominey-Foy, Charlotte Graham, Charlotte Attwood, Shafqat Inam, Alan Dunlop, Katy Sanchez, Kirsty Cuthill and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cancer research communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. TNature communications · 2025
    Article
  3. Article
  4. Review
  5. Quadruple adenine base-edited allogeneic CAR T cells outperform CRISPR/Cas9 nuclease-engineered T cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Review
  7. Article
  8. Review
  9. Are we there yet? CAR-T therapy in multiple myeloma.British journal of haematology · 2024
    Review
  10. Article
  11. Current Novel Targeted Therapeutic Strategies in Multiple Myeloma.International journal of molecular sciences · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Chimeric Antigen Receptor T Cells for the Treatment of Multiple Myeloma.Mediterranean journal of hematology and infectious diseases · 2024
    Review
  17. Review
  18. Review
  19. Review
  20. 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

17 authors at 5 institutions in 2 countries.

Ana M MeteloComprehensive Cancer Center, Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom.ORCID 0000-0002-8990-6145
Agnieszka JozwikComprehensive Cancer Center, Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom.
Le Anh LuongComprehensive Cancer Center, Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom.
Delaney Dominey-FoyComprehensive Cancer Center, Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom.
Charlotte GrahamComprehensive Cancer Center, Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom.
Charlotte AttwoodComprehensive Cancer Center, Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom.
Shafqat InamKing's College Hospital NHS Foundation Trust, London, United Kingdom.
Alan DunlopKing's College Hospital NHS Foundation Trust, London, United Kingdom.
Katy SanchezKing's College Hospital NHS Foundation Trust, London, United Kingdom.
Kirsty CuthillKing's College Hospital NHS Foundation Trust, London, United Kingdom.
Carmel RiceKing's College Hospital NHS Foundation Trust, London, United Kingdom.
Matthew StreetlyGuy's and St. Thomas' NHS Foundation Trust, London, United Kingdom.
Trevor BentleyAllogene Therapeutics Inc., South San Francisco, California.
Bijan BoldajipourPfizer Inc., South San Francisco, California.ORCID 0000-0003-2065-555X
Cesar SommerAllogene Therapeutics Inc., South San Francisco, California.
Barbra SasuAllogene Therapeutics Inc., South San Francisco, California.ORCID 0000-0002-4394-7339
Reuben BenjaminComprehensive Cancer Center, Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom.
London Cancer · GBKing's College Hospital NHS Foundation Trust · GBAllogene Therapeutics (United States) · USGuy's and St Thomas' NHS Foundation Trust · GBThe Fertilizer Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma remains an incurable plasma cell malignancy despite the rapidly evolving treatment landscape. Chimeric antigen receptor T cells targeted against BCMA have recently shown great promise in relapsed refractory multiple myeloma; however, all patients ultimately still progress from their disease. Lack of CAR T-cell persistence, impaired T-cell fitness in autologous CAR T-cell products and the presence of an immunosuppressive bone marrow (BM) microenvironment are contributory factors to treatment failure. We generated anti-BCMA CAR T cells from healthy donors (HD) and patients with multiple myeloma at different stages of disease to compare their T-cell profile, fitness, and cytotoxic activity in preclinical studies. We also used an Significance: Multiple myeloma is an incurable cancer of the plasma cells. A new therapy with anti-BCMA CAR T cells - the patient's own T cells genetically engineered to find and kill myeloma cancer cells - has shown encouraging results. Unfortunately, patients still relapse. In this study, we propose to use T cells from HD volunteers, which have a stronger T-cell fitness, higher cancer killing capacity, and are ready to be administered when needed.

Indexed as

Hematopoietic Stem Cell TransplantationMultiple MyelomaReceptors, Chimeric AntigenGamma Secretase Inhibitors and ModulatorsHumansNeoplasm Recurrence, LocalT-LymphocytesTumor MicroenvironmentGamma Secretase Inhibitors and ModulatorsReceptors, Chimeric Antigen

Identifiers

PMID36874402
PMCPMC9980918
OpenAlexW4221030777

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.