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mHag UTA2-1 loaded PD-L silenced DC vaccination after allo SCT

Conditions
Multipel Myeloma (MM), Chronic Lymphocytic Leukemia (CLL), Non Hodgkin Lymphoma (NHL)
Acute Myeloide Leukemie (AML)
Registration Number
NL-OMON22602
Lead Sponsor
VU University Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
17
Inclusion Criteria

1. Patients with Multiple Myeloma (MM) or Chronic Lymphocytic Leukemia (CLL) or non hodgkin lymphoma (any grade) or acute myeloid leukemia (AML)
2. Recipient and donor have a mismatch in UTA2-1 mHag in the Graft versus Tumor (GvT) direction (recipient UTA2-1 positive, donor UTA2-1 negative).
4. Recipient and donor are positive for HLA-A*0201
5. Age 18-75 years
6. Absence of acute GvHD > grade 2 or extensive chronic GvHD
7. No treatment with immunosuppressive drugs such as prednisone, cyclosporine A and MMF at least 4 weeks prior to planned vaccination date.
8. WHO performance 0-2
9. Absence of severe cardiac hepatic, renal, or metabolic disease
10. Written informed consent

Exclusion Criteria

1. WHO performance 3-4
2. Presence of severe cardiac hepatic, renal, metabolic disease
3. Rapidly progressive disease,
4. Life expectancy < 3 months

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
-To evaluate the toxicity and feasibility of a preemptive minor H ag UTA2-1 peptide-loaded, PD-L silenced donor DC<br> vaccination<br> - To evaluate the effect of minor H ag UTA2-1 peptide-loaded, PD-L1/2 silenced donor DC vaccination on the immune<br> status of the recipient in correlation with the induction of UTA2-1 specific T cell responses after vaccination.
Secondary Outcome Measures
NameTimeMethod
-to evaluate the efficacy of the minor H ag UTA2-1 peptide-loaded, PD-L silenced donor DC vaccination to induce a<br> GvT effect.
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