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Curr Stem Cell Res Ther ; 7(3): 217-28, 2012 May.
Article in English | MEDLINE | ID: mdl-22329580

ABSTRACT

Treatment of metastatic melanoma is a challenge for clinicians as most agents have failed to demonstrate improved survival in phase III trials. Despite the immunogenicity of this tumor entity, different immunological interventions including cytokine therapy, vaccination, biochemotherapy or allogeneic hematopoietic cell transplantation did not lead to a satisfactory response. However, continuous investigation on the immune mediated rejection of melanoma cells has led to the development of effective antibodies blocking cytotoxic T-lymphocyte antigen-4 (CTLA-4), a critical negative regulator of the antitumor T-cell response. Based on data from rodent models, the anti-CTLA-4 antibody ipilimumab was developed into clinical studies where it had encouraging activity in advanced melanoma with unusual response patterns. As in most immunostimulatory therapies, acute toxicities were severe and clearly mechanism-related. Although some patients developed signs of autoimmunity, the toxicities were overall manageable and mostly reversible. This review summarizes different immunotherapeutical approaches against melanoma that have been applied in the past and focuses on CTLA-4 blockade with respect to its mechanism, clinical effectiveness and immunological side effects.


Subject(s)
Antibodies, Monoclonal/therapeutic use , CTLA-4 Antigen/antagonists & inhibitors , Melanoma/therapy , Skin Neoplasms/therapy , T-Lymphocytes, Cytotoxic/drug effects , Antibodies, Monoclonal/administration & dosage , Antibodies, Monoclonal/adverse effects , CTLA-4 Antigen/immunology , Cancer Vaccines/administration & dosage , Clinical Trials, Phase III as Topic , Cytokines/administration & dosage , Hematopoietic Stem Cell Transplantation , Humans , Immunotherapy , Ipilimumab , Melanoma/immunology , Melanoma/pathology , Skin/drug effects , Skin/immunology , Skin/pathology , Skin Neoplasms/immunology , Skin Neoplasms/pathology , T-Lymphocytes, Cytotoxic/immunology , T-Lymphocytes, Cytotoxic/pathology
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