Evidence map›Paper›PMID 37802054›Full record

ArticleCancer cell2023

Cooperative CAR targeting to selectively eliminate AML and minimize escape.

Sascha Haubner, Jorge Mansilla-Soto, Sarah Nataraj, Friederike Kogel, Qing Chang, Elisa de Stanchina, Michael Lopez, Mei Rosa Ng, Kathryn Fraser, Marion Subklewe and 4 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Cancer cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05748197 (A Phase I Study of ADCLEC.syn1 CAR T Cells in Adult Patients With Relapsed or Refractory Acute Myeloid Leukemia), which is not on this map. Cited by 82 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed, 1 pooled it
21.9field-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.

NCT05748197 phase1recruitingnot on this mapstarted 2024, after this paper: background citation

A Phase I Study of ADCLEC.syn1 CAR T Cells in Adult Patients With Relapsed or Refractory Acute Myeloid Leukemia

TypeinterventionalSponsorMemorial Sloan Kettering Cancer CenterRan2024 to 2028Enrolled40ConditionsAcute Myeloid LeukemiaArmsADCLEC.syn1 CAR T cells, Conditioning chemotherapy
3 · Its place in the literature

Who cites it

82 citing papers in PubMed, 1 synthesis or guideline pooled it, 95 citations in OpenAlex.

  1. Mapping the clinical landscape of multifunctional CAR T cells: Targets, trends, and synergies.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Pediatric AML CAR T cell therapy.Molecular therapy. Oncology · 2026
    Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Phase 1 Study of KITE-222, an Autologous CLL-1-Directed CAR T-cell Therapy in Patients with Relapsed/Refractory Acute Myeloid Leukemia.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Adhesion G protein-coupled receptors.Pharmacological reviews · 2026
    Review

22 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 2 countries.

Sascha HaubnerCenter for Cell Engineering, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Jorge Mansilla-SotoCenter for Cell Engineering, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Sarah NatarajCenter for Cell Engineering, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Friederike KogelCenter for Cell Engineering, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Qing ChangAntitumor Assessment Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Elisa de StanchinaAntitumor Assessment Core Facility, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Molecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Michael LopezCenter for Cell Engineering, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Mei Rosa NgTakeda Development Center Americas, Inc., Lexington, MA 02421, USA.
Kathryn FraserTakeda Development Center Americas, Inc., Lexington, MA 02421, USA.
Marion SubkleweDepartment of Medicine III, University Hospital, LMU Munich, 81377 Munich, Germany.
Jae H ParkCenter for Cell Engineering, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Cellular Therapy Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Xiuyan WangCenter for Cell Engineering, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Molecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Michael G. Harris Cell Therapy and Cell Engineering Facility, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Isabelle RivièreCenter for Cell Engineering, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Molecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Michael G. Harris Cell Therapy and Cell Engineering Facility, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Michel SadelainCenter for Cell Engineering, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. Electronic address: m-sadelain@ski.mskcc.org.
Memorial Sloan Kettering Cancer Center · USTakeda (United States) · USLMU Klinikum · DE

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
The Memorial Sloan Kettering Cancer Center SPORE in LeukemiaP50CA254838 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Anthony Folawuyi Daniyan · 2021 to 2026
$16.8M
NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA254838
6 · The paper itself

Abstract

Acute myeloid leukemia (AML) poses a singular challenge for chimeric antigen receptor (CAR) therapy owing to its phenotypic heterogeneity and similarity to normal hematopoietic stem/progenitor cells (HSPCs). Here we expound a CAR strategy intended to efficiently target AML while minimizing HSPC toxicity. Quantification of target expression in relapsed/refractory patient samples and normal HSPCs reveals a therapeutic window for gated co-targeting of ADGRE2 and CLEC12A: We combine an attenuated ADGRE2-CAR with a CLEC12A-chimeric costimulatory receptor (ADCLEC.syn1) to preferentially engage ADGRE2

Indexed as

Leukemia, Myeloid, AcuteT-LymphocytesAnimalsCell Line, TumorHematopoietic Stem CellsHumansImmunotherapy, AdoptiveLectins, C-TypeMiceReceptors, MitogenCLEC12A protein, humanLectins, C-TypeReceptors, Mitogenacute myeloid leukemiaCAR T cell therapychimeric antigen receptorcombinatorial targetingcooperative CARhematotoxicityICAHTIF-BETTER gateoff-target toxicityon-target toxicity

Identifiers

PMID37802054
PMCPMC11006543
OpenAlexW4387378062

What OpenQuestion holds

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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.