Irradiation of Donor Mononuclear Cells for Treatment of Chemorefractory Metastatic Solid Cancers: A Community-Based Immune Transplant Pilot Study / Journal of the Korean Cancer Association, 대한암학회지
Cancer Research and Treatment
;
: 133-141, 2012.
Article
in English
| WPRIM
| ID: wpr-92986
ABSTRACT
PURPOSE:
Chemotherapy has demonstrated ability to generate tumor antigens secondary to induction of apoptosis, against which human leukocyte antigen-compatible, irradiated, related donor mononuclear cells may be administered with immune stimulation to activate antigen presenting and cytotoxic T cells, while minimizing risk of graft-versus-host disease (GVHD). The present study endeavours to describe feasibility and efficacy of this treatment, specifically in the community setting. MATERIALS ANDMETHODS:
Eligible patients had rapidly progressive, chemorefractory metastatic solid tumors. Treatment consisted of intravenous etoposide and cyclosporine for three days followed by granulocyte-macrophage colony-stimulating factor for 5 days. The following week, 5x10(7) haploidentical or more closely matched irradiated donor mononuclear cells were given weekly for 10 weeks along with interleukin-2.RESULTS:
Three patients were enrolled, and the regimen was well-tolerated, with no GVHD observed. All patients had clinical response, despite advanced and heavily pretreated disease.CONCLUSION:
The above-outlined protocol demonstrates favorable tolerability and efficacy, and appears to be feasible in the community setting. While the optimal chemotherapy, immunostimulation, and irradiation regimens may be further optimized, future investigation appears warranted, and may include community oncology programs.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Tissue Donors
/
Leukocytes, Mononuclear
/
T-Lymphocytes
/
Pilot Projects
/
Granulocyte-Macrophage Colony-Stimulating Factor
/
Immunization
/
Cyclosporine
/
Apoptosis
/
Neoplasm, Residual
/
Transplants
Type of study:
Practice guideline
Limits:
Humans
Language:
English
Journal:
Cancer Research and Treatment
Year:
2012
Type:
Article
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