Evidence map›Paper›PMID 28765140›Full record

ReviewEMBO molecular medicine2017

Clinical development of CAR T cells-challenges and opportunities in translating innovative treatment concepts.

Jessica Hartmann, Martina Schüßler-Lenz, Attilio Bondanza, Christian J Buchholz

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in EMBO molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05054257 (Safety and Efficacy of Anti-CD19 Chimeric Antigen Receptor-modified Autologous T Cells), which is not on this map. Cited by 285 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
285citing papers in PubMed, 1 pooled it
28.4field-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.

NCT05054257 phase1recruitingnot on this mapstarted 2021, after this paper: background citation

Safety and Efficacy of Anti-CD19 Chimeric Antigen Receptor-modified Autologous T Cells (CART19) in Patients with Relapsed/refractory CD19+ Acute Lymphoblastic Leukemia and Non-Hodgkin's Lymphoma. a Dose Escalation, Open-label, Phase I Study.

TypeinterventionalSponsorInstitute of Hematology and Blood Transfusion, Czech RepublicRan2021 to 2025Enrolled10ConditionsRelapsed or Refractory B-cell Acute Lymphoblastic Leukemia, Non-Hodgkin's Lymphoma Refractory, Non-Hodgkin's Lymphoma, RelapsedArmsAutologous CAR19 T lymphocytes
3 · Its place in the literature

Who cites it

285 citing papers in PubMed, 1 synthesis or guideline pooled it, 514 citations in OpenAlex.

  1. Pooled it
  2. IL-15 and IL-21 synergy improves anti-tumor efficacy of iPSC-derived cytotoxic T cells in solid tumors.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. CD147 regulates CD8iScience · 2026
    Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Frontiers in immunology · 2026
    Review
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  14. Review
  15. Review
  16. Review
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  18. Article
  19. Article
  20. Review

225 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

4 authors at 3 institutions in 2 countries.

Jessica HartmannMolecular Biotechnology and Gene Therapy, Paul-Ehrlich-Institut, Langen, Germany jessica.hartmann@pei.de christian.buchholz@pei.de.ORCID 0000-0001-9372-8954
Martina Schüßler-LenzDivision of Medical Biotechnology, Paul-Ehrlich-Institut, Langen, Germany.
Attilio BondanzaInnovative immunotherapies, Ospedale San Raffaele, Milano, Italy.
Christian J BuchholzMolecular Biotechnology and Gene Therapy, Paul-Ehrlich-Institut, Langen, Germany jessica.hartmann@pei.de christian.buchholz@pei.de.ORCID 0000-0002-9837-7345
German Cancer Research Center · DEIRCCS Ospedale San Raffaele · ITPaul Ehrlich Institut · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor (CAR) T cell therapy, together with checkpoint inhibition, has been celebrated as a breakthrough technology due to the substantial benefit observed in clinical trials with patients suffering from relapsed or refractory B-cell malignancies. In this review, we provide a comprehensive overview of the clinical trials performed so far worldwide and analyze parameters such as targeted antigen and indication, CAR molecular design, CAR T cell manufacturing, anti-tumor activities, and related toxicities. More than 200 CAR T cell clinical trials have been initiated so far, most of which aim to treat lymphoma or leukemia patients using CD19-specific CARs. An increasing number of studies address solid tumors as well. Notably, not all clinical trials conducted so far have shown promising results. Indeed, in a few patients CAR T cell therapy resulted in severe adverse events with fatal outcome. Of note, less than 10% of the ongoing CAR T cell clinical trials are performed in Europe. Taking lead from our analysis, we discuss the problems and general hurdles preventing efficient clinical development of CAR T cells as well as opportunities, with a special focus on the European stage.

Indexed as

ImmunotherapyClinical Trials as TopicHumansLeukemiaLymphoma, B-CellReceptors, Antigen, T-CellT-LymphocytesReceptors, Antigen, T-CellATMPscancerimmunotherapyregulatory issuestoxicities

Identifiers

PMID28765140
PMCPMC5582407
OpenAlexW2740938625

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.