French Register Of Patients With Hemopathy Eligible For CAR-T Cell Treatment (DESCAR-T)

This study is a registry including prospective and retrospective data on all patients who have been presented in a Multidisciplinary tumor board or RCP to be eligible for CAR-T cell treatment.

Study Overview

Study Type

Observational

Enrollment (Estimated)

5000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Amiens, France
        • Recruiting
        • CHU d'Amiens - Hôpital Sud
        • Contact:
      • Angers, France
      • Besançon, France
        • Recruiting
        • CHRU Besançon - Hôpital Minjoz
        • Contact:
          • Adrien CHAUCHET, MD
      • Brest, France
      • Caen, France
        • Recruiting
        • Institut d'Hématologie de Basse Normandie
        • Contact:
      • Clermont-Ferrand, France
      • Créteil, France
        • Recruiting
        • APHP - Hopital Henri Mondor
        • Contact:
      • Dijon, France
      • La Tronche, France
        • Recruiting
        • CHU de Grenoble
        • Contact:
      • Lille, France
        • Recruiting
        • CHRU de Lille - Hôpital Claude Hurriez
        • Contact:
      • Limoges, France
      • Lyon, France
        • Recruiting
        • Centre Léon Bérard
      • Lyon, France
        • Recruiting
        • Institut d'Hématologie et d'Oncologie Pédiatrique (IHOP)
        • Contact:
      • Marseille, France
      • Marseille, France
        • Recruiting
        • Institut Paoli Calmette
        • Contact:
          • Aude Collignon, MD
      • Montpellier, France
      • Nantes, France
      • Nice, France
        • Recruiting
        • CHU de Nice
        • Contact:
      • Paris, France
      • Paris, France
        • Recruiting
        • APHP - Hôpital Saint Antoine
        • Contact:
      • Paris, France
        • Recruiting
        • APHP - Hôpital Necker
        • Contact:
      • Paris, France
        • Recruiting
        • APHP - Hopital Saint Louis
        • Contact:
      • Paris, France
        • Recruiting
        • APHP - Hôpital La Pitié Salpêtrière
        • Contact:
      • Paris, France
        • Recruiting
        • APHP - Hôpital Universitaire Robert Debré
        • Contact:
      • Pessac, France
      • Pierre-Bénite, France
        • Recruiting
        • Centre Hospitalier Lyon sud
        • Contact:
      • Poitiers, France
        • Recruiting
        • Hôpital de la Milétrie - CHU de Poitiers
        • Contact:
      • Rennes, France
      • Rouen, France
      • Rouen, France
      • Saint-Priest-en-Jarez, France
        • Recruiting
        • Institut de Cancérologie Hématologie Universitaire de Saint Etienne
        • Contact:
      • Strasbourg, France
        • Recruiting
        • ICANS (Institut de Cancérologie Strasbourg Europe)
        • Contact:
      • Toulouse, France
        • Recruiting
        • Institut Universitaire du Cancer - Oncopole Toulouse (IUCT-O)
        • Contact:
      • Tours, France
        • Recruiting
        • CHU Bretonneau
        • Contact:
      • Vandœuvre-lès-Nancy, France
        • Recruiting
        • CHU Brabois
        • Contact:
        • Principal Investigator:
          • Marie-Thérèse RUBIO, Pr
        • Principal Investigator:
          • Cécile POCHON, MD
      • Villejuif, France

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

1 second to 99 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Patient eligible for a treatment with CAR-T for an hematological malignancy

Description

Inclusion Criteria:

Retrospective inclusion :

  • Patient treated with CAR-T from 1 July 2018 under temporary authorization (ATU) or covered by French health insurance system (under post-ATU or MA) in a qualified center before activation of this register in this center
  • If the patient is alive, the patient has been informed of the collection and use of their data, and the patient has not opposed this use. If the patient has died, the patient did not opposed the use of their data while alive

Prospective inclusion :

  • Patient eligible for a treatment with CAR-T for an hematological malignancy which is covered by French health insurance (for ATUs / post-ATUs or MA), or as part of a clinical trial with the same indication, after the activation of this register in this center.
  • Patient whose CAR-T indication has been validated during a multidisciplinary tumor board (RCP) of a qualified center, according to the ministerial order of 8 August 2019
  • Patient deemed eligible for a treatment with CAR-T after a medical exam performed in a qualified center according to the ministerial order of 8 August 2019
  • If the patient is alive, the patient has been informed of the collection and use of their data, and the patient has not opposed this use. If the patient has died, the patient did not opposed the use of their data while alive.

Exclusion Criteria Patient not registered with the social security in France

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Other

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
overall survival from eligibility
Time Frame: 15 years
15 years
Overall survival from administration
Time Frame: 15 years
15 years
complete response rate
Time Frame: 15 years
15 years
Progression free survival
Time Frame: 15 years
15 years
Duration of response
Time Frame: 15 years
15 years
Delays between patient eligibility and CAR-T treatment
Time Frame: 15 years
15 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Steven LE GOUILL, Pr, Institut CURIE
  • Principal Investigator: Roch HOUOT, Pr, CHU Pontchaillou

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 19, 2019

Primary Completion (Estimated)

December 19, 2038

Study Completion (Estimated)

December 19, 2038

Study Registration Dates

First Submitted

March 27, 2020

First Submitted That Met QC Criteria

March 27, 2020

First Posted (Actual)

March 31, 2020

Study Record Updates

Last Update Posted (Actual)

March 4, 2026

Last Update Submitted That Met QC Criteria

March 2, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • DESCAR-T

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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