Evidence map›Paper›PMID 31907405›Full record

ArticleNature biotechnology2020

The therapeutic landscape for cells engineered with chimeric antigen receptors.

Matthew MacKay, Ebrahim Afshinnekoo, Jonathan Rub, Ciaran Hassan, Mihir Khunte, Nithyashri Baskaran, Bryan Owens, Lauren Liu, Gail J Roboz, Monica L Guzman and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature biotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 152 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
152citing papers in PubMed, 2 pooled it
–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

152 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Genes & diseases · 2025
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review

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

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

13 authors.

Matthew MacKayDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, USA.
Ebrahim AfshinnekooDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, USA.
Jonathan RubDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, USA.
Ciaran HassanYale University, New Haven, CT, USA.
Mihir KhunteYale University, New Haven, CT, USA.
Nithyashri BaskaranYale University, New Haven, CT, USA.
Bryan OwensYale University, New Haven, CT, USA.
Lauren LiuYale University, New Haven, CT, USA.
Gail J RobozDivision of Hematology/Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
Monica L GuzmanDivision of Hematology/Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0002-9262-8246
Ari M MelnickDivision of Hematology/Oncology, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0002-8074-2287
Shixiu WuNational Cancer Center/National Clinical Research Center for Cancer, Cancer Hospital & Shenzhen Hospital, Shenzhen, China. wushixiu@zju.edu.cn.
Christopher E MasonDepartment of Physiology and Biophysics, Weill Cornell Medicine, New York, NY, USA. chm2042@med.cornell.edu.ORCID http://orcid.org/0000-0002-1850-1642

Funding

Project 3: Targeting PRMT5 in Mantle Cell LymphomaP01CA214274 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI BAIOCCHI, ROBERT ALAN · 2018 to 2022
$8.9M
Targeting Epigenetic Circuits in B-Cell LymphomasR35CA220499 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI MELNICK, ARI M. · 2018 to 2024
$7.2M
The Spatiotemporal Landscape of the Human Brain EpitranscriptomeR01MH117406 · NIMH · WEILL MEDICAL COLL OF CORNELL UNIV · PI MASON, CHRISTOPHER EDWARD · 2018 to 2022
$3.3M
Therapeutic targeting of SIRT3 for aggressive and refractory lymphomasR01CA270243 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI Meng Li · 2023 to 2026
$2.7M
NCI NIH HHS P01 CA214274NCI NIH HHS R01 CA270243NCI NIH HHS R35 CA220499NIMH NIH HHS R01 MH117406
6 · The paper itself

Abstract

Despite the global rapid increase in the number of clinical trials employing chimeric antigen receptors (CARs), no comprehensive survey of their scope, targets and design exists. In this study, we present an interactive CAR clinical trial database, spanning 64 targets deployed in T cells (CAR-T), natural killer cells (CAR-NK) or mixtures (CAR-NK/T) from over 500 clinical trials in 20 countries, encompassing >20,000 patients. By combining these data with transcriptional and proteomic data, we create a 'targetable landscape' for CAR cell therapies based on 13,206 proteins and RNAs across 78 tissues, 124 cell types and 20 cancer types. These data suggest a landscape of over 100 single targets and over 100,000 target pairs using logical switches for CAR cell engineering. Our analysis of the CAR cellular therapeutic landscape may aid the design of future therapies, improve target-to-patient matching, and ultimately help inform our understanding of CAR therapy's safety and efficacy.

Indexed as

Cell- and Tissue-Based TherapyCell EngineeringClinical Trials as TopicGene Expression Regulation, NeoplasticHumansNeoplasmsReceptors, Chimeric AntigenReceptors, Chimeric Antigen

Identifiers

What OpenQuestion holds

Textmetadata
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.