No registrations found.
ID
Source
Brief title
Health condition
high risk leukemia
Sponsors and support
Intervention
Outcome measures
Primary outcome
1. The number of events of acute GvHD, all other adverse events and death;
2. The feasibility of generation of HA-1 TCR transduced virus-specific donor T-cells.
Secondary outcome
1. The number of HA-1 TCR transduced virus-specific donor T-cells in blood or bone marrow at different time points;
2. The number of patients eligible for standard DLI at 6 months.
Background summary
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.
Study objective
N/A
Study design
1. Weekly, first 8 weeks after infusion(s);
2. Three weekly, next 2-3 months.
Intervention
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.
P. Balen, van
Leiden 2300 RC
The Netherlands
+31 (0)71 5262267
stafsecretariaathematologie@lumc.nl
P. Balen, van
Leiden 2300 RC
The Netherlands
+31 (0)71 5262267
stafsecretariaathematologie@lumc.nl
Inclusion criteria
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.
Exclusion criteria
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.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL3307 |
NTR-old | NTR3454 |
Other | METC LUMC : 2010-03 |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |