Evidence map›Paper›PMID 36692420›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2023

Allogeneic CAR T Cells Targeting DLL3 Are Efficacious and Safe in Preclinical Models of Small Cell Lung Cancer.

Yi Zhang, Silvia K Tacheva-Grigorova, Janette Sutton, Zea Melton, Yvonne S L Mak, Cecilia Lay, Bryan A Smith, Tao Sai, Thomas Van Blarcom, Barbra J Sasu and 1 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06348797 (Phase I Clinical Study on Safety and Feasibility of DLL3 Targeted α-PD-L1/4-1BB Modifying Chimeric Antigen Receptor T-cells in Patients With Relapsed or Refractory Small Cell Lung Cancer), which is not on this map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
10.6field-weighted citation impact, top 1% 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.

NCT06348797 phase1recruitingnot on this mapstarted 2025, after this paper: background citation

Phase I Clinical Study on Safety and Feasibility of DLL3 Targeted α-PD-L1/4-1BB Modifying Chimeric Antigen Receptor T-cells in Patients With Relapsed or Refractory Small Cell Lung Cancer (SCLC)

TypeinterventionalSponsorSichuan UniversityRan2025 to 2026Enrolled30ConditionsSmall Cell Lung Cancer Extensive StageArmsα-PD-L1/4-1BB DLL3 CAR-T (BHP01)
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Review
  3. Adoptive cell therapies in thoracic malignancies: a comprehensive review.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. The Five-Decade Journey of Small Cell Lung Cancer.Cancer communications (London, England) · 2026
    Review
  9. Review
  10. Review
  11. Review
  12. The next generation of immunotherapies for lung cancers.Nature reviews. Clinical oncology · 2025
    Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. New developments in immunotherapy for SCLC.Journal for immunotherapy of cancer · 2025
    Review
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Yi ZhangAllogene Therapeutics, South San Francisco, California.ORCID 0000-0003-1878-343X
Silvia K Tacheva-GrigorovaAllogene Therapeutics, South San Francisco, California.ORCID 0000-0002-9665-4193
Janette SuttonAllogene Therapeutics, South San Francisco, California.ORCID 0000-0002-4580-9319
Zea MeltonAllogene Therapeutics, South San Francisco, California.ORCID 0000-0002-9912-9968
Yvonne S L MakAllogene Therapeutics, South San Francisco, California.ORCID 0000-0001-8052-5293
Cecilia LayAllogene Therapeutics, South San Francisco, California.ORCID 0000-0001-5896-0416
Bryan A SmithAllogene Therapeutics, South San Francisco, California.ORCID 0000-0002-7011-7648
Tao SaiPfizer Worldwide Research and Development, South San Francisco, California.ORCID 0000-0002-9226-4016
Thomas Van BlarcomAllogene Therapeutics, South San Francisco, California.ORCID 0000-0003-0111-1661
Barbra J SasuAllogene Therapeutics, South San Francisco, California.ORCID 0000-0002-4394-7339
Siler H PanowskiAllogene Therapeutics, South San Francisco, California.ORCID 0000-0001-7488-3086
Allogene Therapeutics (United States) · USAIR Worldwide (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeSmall cell lung cancer (SCLC) is an aggressive disease with limited treatment options. Delta-like ligand 3 (DLL3) is highly expressed on SCLC and several other types of neuroendocrine cancers, with limited normal tissue RNA expression in brain, pituitary, and testis, making it a promising CAR T-cell target for SCLC and other solid tumor indications. EXPERIMENTAL

designA large panel of anti-DLL3 scFv-based CARs were characterized for both in vitro and in vivo activity. To understand the potential for pituitary and brain toxicity, subcutaneous or intracranial tumors expressing DLL3 were implanted in mice and treated with mouse cross-reactive DLL3 CAR T cells.

resultsA subset of CARs demonstrated high sensitivity for targets with low DLL3 density and long-term killing potential in vitro. Infusion of DLL3 CAR T cells led to robust antitumor efficacy, including complete responses, in subcutaneous and systemic SCLC in vivo models. CAR T-cell infiltration into intermediate and posterior pituitary was detected, but no tissue damage in brain or pituitary was observed, and the hormone-secretion function of the pituitary was not ablated.

conclusionsIn summary, the preclinical efficacy and safety data presented here support further evaluation of DLL3 CAR T cells as potential clinical candidates for the treatment of SCLC.

Indexed as

Hematopoietic Stem Cell TransplantationLung NeoplasmsSmall Cell Lung CarcinomaAnimalsIntracellular Signaling Peptides and ProteinsLigandsMaleMembrane ProteinsMiceT-LymphocytesDll3 protein, mouseIntracellular Signaling Peptides and ProteinsLigandsMembrane Proteins

Identifiers

PMID36692420
OpenAlexW4317868962

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.