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A Study of the Safety and Efficacy of EBV Specific T-cell Lines

Lymphoma | Epstein-Barr Virus Infections | Post-Transplant Lymphoproliferative Disorder

This study evaluates the safety and efficacy of EBV-specific T-cell lines to treat patients suffering from high EBV viral titers not responding to standard of care therapies and to treat EBV-related lymphoma. The study will recruit 6 patients to receive autologous T cells or a T cell line derived from the patient's allogeneic donor (in the case of stem cell transplant recipients), and 6 patients to receive a T-cell line prepared from a matched or partially matched related donor.

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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    18 and up

Critères de participation

Inclusion Criteria:

* Capacity to provide informed consent
* Age ≥ 18 years old
* Confirmed treatment-refractory EBV reactivation or EBV-related lymphoma
* ECOG of 2 or less

Exclusion Criteria:

* Medical condition requiring a corticosteroid dose greater than Prednisone 0.5mg/kg/day (or equivalent) at the time of the infusion.
* Patient has received T-cell depleting antibodies or stem cell transplantation in the 28 days prior to proposed date of anti-EBV T-cell line infusion
* Patient has received a solid organ transplant in the 3 months prior to proposed date of anti-EBV T-cell line infusion.
* Pregnant or nursing females
* Life expectancy of less than 3 months due to a condition unrelated to the EBV- related disease.
* Active uncontrolled GVHD
* Active uncontrolled SOT rejection episode

DONOR ELIGIBILITY: An allogeneic donor must be a first-degree relative with at least 3/6 HLA compatibility, have consented to donate peripheral blood mononuclear cells, and fulfill the same criteria for stem cell donation according to the hospital's standard operating procedure.

Lieu de l'étude

Hôpital Maisonneuve-Rosemont
Hôpital Maisonneuve-Rosemont
Montreal, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Jean-Sébastien Delisle, MD, PhD

[email protected]
5142523404
Backup Contact

Stéphanie Thiant, PhD

[email protected]
5142523404
Étude parrainée par
Maisonneuve-Rosemont Hospital
Participants recherchés
Plus d'informations
ID de l'étude: NCT02580539