Evidence map›Paper›PMID 39863732›Full record

ArticleBone marrow transplantation2025

Identification of the conditions and minimum requirements necessary for the release of autologous fresh CAR T-cell products under hospital exemption: a position paper from the WP-bioproduction of the UNITC consortium.

Olivier Boyer, Daniele Bensoussan, Halvard Bönig, Christian Chabannon, Béatrice Clémenceau, Alexis Cuffel, Guillaume Dachy, John de Vos, Sophie Derenne, Jean-Sébastien Diana and 14 more

Abstract readConsensus Statement
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Article
  3. Review
  4. Review
  5. Review
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

24 authors.

Olivier BoyerUniv Rouen Normandie, Inserm, UMR 1234, CHU de Rouen, Department of Immunology and Biotherapy, F-76000, Rouen, France. olivier.boyer@chu-rouen.fr.
Daniele BensoussanCHRU de Nancy, Unité de Thérapie cellulaire et Banque de Tissus (UTCT). Université de Lorraine, UMR 7365 IMoPA, Vandoeuvre-les-Nancy, France.
Halvard BönigGoethe University, Faculty of Medicine, Institute for Transfusion Medicine and Immunohematology, Frankfurt a.M., Germany.
Christian ChabannonCentre de Thérapie Cellulaire, Institut Paoli-Calmettes (IPC) & module Biothérapies du Centre d'Investigations Cliniques de Marseille, Inserm CBT-1409 / Aix-Marseille Université / AP-HM / IPC, Marseille, France.ORCID 0000-0002-3755-4889
Béatrice ClémenceauUnité de Thérapie Cellulaire et Génique (UTCG), CHU de Nantes, Nantes, France.
Alexis CuffelCHU de Rouen, Laboratoire d'Immunologie et de Biothérapies, Université de Rouen Normandie, Inserm, UMR 1234, F-76000, Rouen, France.
Guillaume DachyCHU de Rouen, Laboratoire d'Immunologie et de Biothérapies, Université de Rouen Normandie, Inserm, UMR 1234, F-76000, Rouen, France.ORCID 0000-0002-1668-975X
John de VosDepartment of Cell and Tissue Engineering, University Montpellier, CHU Montpellier, F-34000, Montpellier, France.ORCID 0000-0003-1880-4130
Sophie DerenneEtablissement Français du Sang, La Plaine Saint Denis, Paris, France.
Jean-Sébastien DianaAPHP, Hôpital Universitaire Necker Enfants Malades, Centre d'Investigation Clinique en Biothérapie, Laboratoire de Thérapie Cellulaire et Génique, Paris, France.
Aurore DougéCHU de Clermont-Ferrand, Service Oncologie médicale, EA 7453 Chelter Université Clermont Auvergne, 63000, Clermont-Ferrand, France.
Laure DeramoudtCHU de Lille, PUI, 59000, Lille, France.
Christophe FerrandUniversité de Franche-Comté, EFS, INSERM, UMR RIGHT, F-, 25000, Besançon, France.ORCID 0000-0003-0119-3919
Edouard ForcadeCHU de Bordeaux, Service Hématologie Clinique et Thérapie Cellulaire, UMR 5164, F-33000, Bordeaux, France.ORCID 0000-0002-8873-2868
Jeanne GalaineUniversité de Franche-Comté, EFS, INSERM, UMR RIGHT, F-, 25000, Besançon, France.
Anne GalyART-TG, Inserm, US35, 91100, Corbeil-Essonnes, France.
Camille GiverneCHU de Rouen, Laboratoire d'Immunologie et de Biothérapies, Université de Rouen Normandie, Inserm, UMR 1234, F-76000, Rouen, France.
Jérémie MartinetUniv Rouen Normandie, Inserm, UMR 1234, CHU de Rouen, Department of Immunology and Biotherapy, F-76000, Rouen, France.
Chrystel MartonCHU de Lille, service des maladies du sang, 59000, Lille, France.
Jérôme LargheroAP-HP, Université Paris Cité, Hôpital Saint-Louis, Centre MEARY de Thérapie Cellulaire et Génique, Unité de Thérapie Cellulaire, Centre d'Investigation Clinique en Biothérapies, Inserm, Paris, France.
Loïc ReppelCHRU de Nancy, Unité de Thérapie cellulaire et Banque de Tissus (UTCT). Université de Lorraine, UMR 7365 IMoPA, Vandoeuvre-les-Nancy, France.
Sébastien VielPlateforme de biothérapies - Médicaments de Thérapie Innovante, Hôpital Edouard Herriot, Hospices Civils de Lyon, 69003, Lyon, France.ORCID 0000-0002-5085-443X
Ibrahim Yakoub-AghaCHU de Lille, Univ Lille, INSERM U1286, Infinite, 59000, Lille, France.
Marina DeschampsUniversité de Franche-Comté, EFS, INSERM, UMR RIGHT, F-, 25000, Besançon, France. marina.deschamps@efs.sante.fr.ORCID 0000-0002-0564-0926

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The accessibility of CAR-T cells in centralized production models faces significant challenges, primarily stemming from logistical complexities and prohibitive costs. However, European Regulation EC No. 1394/2007 introduced a pivotal provision known as the hospital exemption. This exemption enables academic institutions to produce ATMPs, including autologous CAR-T cells, under GMP conditions tailored to specific needs. In response to this regulatory framework, our work group has launched a guideline initiative. This endeavor aims to bolster academic CAR T-cell manufacturing by implementing strategic workshops that serve a dual purpose: standardizing production processes and ensuring both efficacy and safety standards are met. This inaugural focused on delineating criteria for the release of fresh CAR-T cell batches. Key emphases included thorough product characterization, stringent safety and potency evaluations. These criteria are essential for compliance with regulatory mandates and aligning with industry best practices. Notably, the release of initial CAR T-cell batches will be facilitated through provisional certification, with final certification contingent upon the acquisition of comprehensive analytical control results. This procedural framework adheres to methodologies endorsed by the SFGM-TC and the EBMT. Such adherence underscores a commitment to harmonizing practices across academic manufacturing facilities, thus fortifying the accessibility, efficacy, and safety of point-of-care units.

Indexed as

Immunotherapy, AdoptiveReceptors, Chimeric AntigenT-LymphocytesHumansReview Literature as TopicReceptors, 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.