Lymphoma Clinical Trial
Official title:
Immune Reconstitution After Autologous Hematopoietic Stem Cell Transplantation for High-Risk Lymphoma and Myeloma
RATIONALE: Vaccines may help the body build an effective immune response to kill cancer
cells. Giving vaccine therapy after an autologous stem cell transplant may kill any cancer
cells that remain after transplant.
PURPOSE: This clinical trial is studying how well vaccine therapy works in treating patients
who have undergone autologous stem cell transplant for high-risk lymphoma or multiple
myeloma.
OBJECTIVES:
Primary
- Assess immune reconstitution as measured by response to pneumococcal polyvalent vaccine,
NK-cell activity against autologous lymphoblastoid cell lines, and cytomegalovirus and
Epstein-Barr virus tetramer responses in patients who have undergone autologous
hematopoietic stem cell transplantation for high-risk lymphoma or multiple myeloma.
Secondary
- Assess the absolute number of circulating regulatory T-cells and the function of these
cells as measured by their expression of TGFβ and interleukin-10 (IL-10).
- Evaluate the effect of conditioning therapy on quality of life, including functional
status, fatigue, and depression, in these patients.
- Correlate quality of life with inflammatory cytokine production of peripheral blood
monocytes at specified time points.
- Provide baseline immune reconstitution and quality of life pilot data for comparison in
future post-transplant immunotherapy trials.
OUTLINE: Patients receive pneumococcal polyvalent vaccine intramuscularly once in weeks 9,
17, and 25 after autologous hematopoietic stem cell transplantation.
Blood samples are collected periodically for correlative and immunological studies.
Quality of life (QOL) is assessed periodically using the QOL short form (SF-36, 4-week
version), the Center for Epidemiologic Studies Depression scale (CES-D), and the
Multidimensional Fatigue Symptom Inventory (MFSI-30).
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