Co-immunotherapy with interleukin-2 and taurolidine for progressive metastatic melanoma.
dc.contributor.author | O'Brien, G C | |
dc.contributor.author | Cahill, R A | |
dc.contributor.author | Bouchier-Hayes, D J | |
dc.contributor.author | Redmond, H P | |
dc.date.accessioned | 2012-02-03T15:05:28Z | |
dc.date.available | 2012-02-03T15:05:28Z | |
dc.date.issued | 2012-02-03T15:05:28Z | |
dc.identifier.citation | Ir J Med Sci. 2006 Jan-Mar;175(1):10-4. | en_GB |
dc.identifier.issn | 0021-1265 (Print) | en_GB |
dc.identifier.issn | 0021-1265 (Linking) | en_GB |
dc.identifier.pmid | 16615221 | en_GB |
dc.identifier.uri | http://hdl.handle.net/10147/208852 | |
dc.description.abstract | BACKGROUND: Recombinant interleukin-2(rIL-2) therapy in metastatic melanoma is limited by toxicities, particularly vascular leak syndrome(VLS). Taurolidine potentiates the anti-neoplastic effects of IL-2 while reducing its associated endothelial cell dysfunction in experimental settings. We hypothesized that co-administration of rIL-2 with taurolidine could enhance tolerability without weakening effectiveness. METHODS: Eleven patients with progressive metastatic melanoma received high-dose rIL-2 with co-infusion of taurolidine. Patients were monitored for the development of toxicities and evidence of response. RESULTS: Ten patients tolerated twenty-nine courses of high-dose rIL-2 without dose-reduction. Most toxicities were low-grade. No patient developed VLS. Seven patients died from disease progression. Two had complete clinical and radiological responses to treatment. Two patients remain alive despite evidence of disease progression a mean of 17.5 months after diagnosing metastatic disease. CONCLUSION: Co-administration of taurolidine with high-dose rIL-2 in stage IV melanoma patients appears to greatly enhance the tolerability of this regime without diminishing its therapeutic value. | |
dc.language.iso | eng | en_GB |
dc.subject.mesh | Adult | en_GB |
dc.subject.mesh | Drug Combinations | en_GB |
dc.subject.mesh | Female | en_GB |
dc.subject.mesh | Humans | en_GB |
dc.subject.mesh | Immunotherapy | en_GB |
dc.subject.mesh | Interleukin-2/*therapeutic use | en_GB |
dc.subject.mesh | Ireland | en_GB |
dc.subject.mesh | Male | en_GB |
dc.subject.mesh | Melanoma/*drug therapy/secondary | en_GB |
dc.subject.mesh | Middle Aged | en_GB |
dc.subject.mesh | Skin Neoplasms/*drug therapy/*secondary | en_GB |
dc.subject.mesh | Taurine/*analogs & derivatives/therapeutic use | en_GB |
dc.subject.mesh | Thiadiazines/*therapeutic use | en_GB |
dc.title | Co-immunotherapy with interleukin-2 and taurolidine for progressive metastatic melanoma. | en_GB |
dc.contributor.department | Dept of Academic Surgery, Cork University Hospital and NUI. | en_GB |
dc.identifier.journal | Irish journal of medical science | en_GB |
dc.description.province | Munster | |
html.description.abstract | BACKGROUND: Recombinant interleukin-2(rIL-2) therapy in metastatic melanoma is limited by toxicities, particularly vascular leak syndrome(VLS). Taurolidine potentiates the anti-neoplastic effects of IL-2 while reducing its associated endothelial cell dysfunction in experimental settings. We hypothesized that co-administration of rIL-2 with taurolidine could enhance tolerability without weakening effectiveness. METHODS: Eleven patients with progressive metastatic melanoma received high-dose rIL-2 with co-infusion of taurolidine. Patients were monitored for the development of toxicities and evidence of response. RESULTS: Ten patients tolerated twenty-nine courses of high-dose rIL-2 without dose-reduction. Most toxicities were low-grade. No patient developed VLS. Seven patients died from disease progression. Two had complete clinical and radiological responses to treatment. Two patients remain alive despite evidence of disease progression a mean of 17.5 months after diagnosing metastatic disease. CONCLUSION: Co-administration of taurolidine with high-dose rIL-2 in stage IV melanoma patients appears to greatly enhance the tolerability of this regime without diminishing its therapeutic value. |