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Evaluation of Immunological Reconstitution After Haploidentical Bone Marrow Transplantation

Conditions
Lymphoma
Registration Number
NCT01891578
Lead Sponsor
Armando Santoro, MD
Brief Summary

Evaluation of immunological reconstitution after haploidentical BMT using a nonmyeloablative preparative regimen and post-transplant cyclophosphamide in patients with poor prognosis lymphoma

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
23
Inclusion Criteria
  • Patients with lymphoma (any histology) relapsed after high dose chemotherapy and in partial remission, complete remission or stable disease after the last CT line that
  • Signed informed consent to perform an haploidentical allo-BMT using a nonmyeloablative preparative regimen and post-transplant cyclophosphamide
Exclusion Criteria

none

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Evaluation of T lymphocytes and NK cells absolute number1 year
Secondary Outcome Measures
NameTimeMethod
Evaluation of discrete T-cells populations1 year

Evaluation, by flow cytometry, of discrete T cell populations, including CD4+ and CD8+ TN, TSCM, TCM and TEM, NK and NKT cells, B cells, dendritic cell subsets

Evaluation of antigen-specific T cell populations1 year

Evaluation of antigen-specific T cell frequency towards CMV, EBV and influenza virus by MHC tetramers

Evaluation of antigen-specific T lymphocyte's functionality1 year

antigen-specific T lymphocyte's functionality towards tumor cell line evaluated using a degranulation assay

Evaluation of cytokines production by IL-2 and anti-CD16 activated NK cells1 year

Trial Locations

Locations (1)

Istituto Clinico Humanitas

🇮🇹

Rozzano, MI, Italy

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