N/A
ID
Bron
Verkorte titel
Aandoening
high risk leukemia
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
1. The number of events of acute GvHD, all other adverse events and death;<br>
2. The feasibility of generation of HA-1 TCR transduced virus-specific donor T-cells.
Achtergrond van het onderzoek
This is an open-label non-randomized phase I/II feasibility study to treat patients with high-risk leukemia with HA-1 TCR
transduced virus-specific donor-derived T-cells 8 and 14 weeks after allo-SCT.
The HA-1 TCR transduced virus-specific T-cells will be generated from donor leukocytes obtained from a leukapheresis product of the stem cell donor. Minimally one and maximally two CMV- and/or EBV-specific T cell populations will be isolated from PBMC using Streptamers. After 2-3 days of culture, virus-specific T-cells are transduced with a retroviral vector encoding the HA-1-TCR. After 8-12 days of additional culturing, the transduced virus-specific T-cells will be analyzed for virus-specific T-cell purity and HA-1-TCR cell surface expression using virus- and HA-1-specific tetramers. For release of the HA-1-TCR transduced virus-specific T-cells, ¡Ý 95% of the cell product must be T-cells, ¡Ý 60% of T-cells must be antigen-specific as measured with tetramers specific for the endogenous virus-TCR and introduced HA-1-TCR, and ¡Ý5% of lymphocytes must be HA-1-tetramer positive. The maximal amount of virus- or HA-1-tetramer negative T-cells with unknown specificity administered in the T-cell product is <0.3 x 106 cells/kg body weight in patients transplanted with HLA-matched related donors and <0.15 x 106 cells/kg body weight in patients transplanted with unrelated donors or HLA-A2 mismatched donors.
Doel van het onderzoek
N/A
Onderzoeksopzet
1. Weekly, first 8 weeks after infusion(s);
2. Three weekly, next 2-3 months.
Onderzoeksproduct en/of interventie
Infusion of manipulated donor lymphocytes consisting HA-1 T-cell receptor (TCR) transduced virus-specific donor T-cells 8 weeks after allogeneic stem cell transplantation (allo-SCT). This infusion may be repeated 6 weeks later.
Publiek
P. Balen, van
Leiden 2300 RC
The Netherlands
+31 (0)71 5262267
stafsecretariaathematologie@lumc.nl
Wetenschappelijk
P. Balen, van
Leiden 2300 RC
The Netherlands
+31 (0)71 5262267
stafsecretariaathematologie@lumc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Age 18-75 years;
2. WHO performance score 0-2;
3. High-risk leukemia;
4. Complete remission (CR) or stable partial remission (PR);
5. HLA-A*0201 positive;
6. HA-1h positive;
7. Availability of a suitable donor;
8. Written informed consent.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Life expectation < 3 months;
2. End stage irreversible multi-system organ failure;
3. Pregnant or lactating women;
4. Severe psychological disturbances;
5. HIV-positivity.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL3307 |
NTR-old | NTR3454 |
Ander register | METC LUMC : 2010-03 |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |