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Clinical Benefit from Ipilimumab Therapy in Melanoma Patients may be Associated with Serum CTLA4 Levels
Stage IV metastatic melanoma patients historically have a poor prognosis with 5–10% 5-year survival. Ipilimumab, a monoclonal antibody against cytotoxic T-lymphocyte antigen 4 (CTLA4), is one of the first treatments to provide beneficial durable responses in advanced melanoma. However, less than 25%...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032905/ https://www.ncbi.nlm.nih.gov/pubmed/24904825 http://dx.doi.org/10.3389/fonc.2014.00110 |
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author | Leung, Anna M. Lee, Agnes Fermin Ozao-Choy, Junko Ramos, Romela Irene Hamid, Omid O’Day, Steven J. Shin-Sim, Myung Morton, Donald L. Faries, Mark B. Sieling, Peter A. Lee, Delphine J. |
author_facet | Leung, Anna M. Lee, Agnes Fermin Ozao-Choy, Junko Ramos, Romela Irene Hamid, Omid O’Day, Steven J. Shin-Sim, Myung Morton, Donald L. Faries, Mark B. Sieling, Peter A. Lee, Delphine J. |
author_sort | Leung, Anna M. |
collection | PubMed |
description | Stage IV metastatic melanoma patients historically have a poor prognosis with 5–10% 5-year survival. Ipilimumab, a monoclonal antibody against cytotoxic T-lymphocyte antigen 4 (CTLA4), is one of the first treatments to provide beneficial durable responses in advanced melanoma. However, less than 25% of those treated benefit, treatment is expensive, and side effects can be fatal. Since soluble (s) CTLA4 may mediate inhibitory effects previously ascribed to the membrane-bound isoform (mCTLA4), we hypothesized patients benefiting from ipilimumab have higher serum levels of sCTLA4. We found that higher sCTLA4 levels correlated both with response and improved survival in patients treated with ipilimumab in a small patient cohort [patients with (n = 9) and without (n = 5) clinical benefit]. sCTLA4 levels were statistically higher in ipilimumab-treated patients with response to ipilimumab. In contrast, sCTLA4 levels did not correlate with survival in patients who did not receive ipilimumab (n = 11). These preliminary observations provide a previously unrecognized link between serum sCTLA4 levels and response to ipilimumab as well as to improved survival in ipilimumab-treated melanoma patients and a potential mechanism by which ipilimumab functions. |
format | Online Article Text |
id | pubmed-4032905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40329052014-06-05 Clinical Benefit from Ipilimumab Therapy in Melanoma Patients may be Associated with Serum CTLA4 Levels Leung, Anna M. Lee, Agnes Fermin Ozao-Choy, Junko Ramos, Romela Irene Hamid, Omid O’Day, Steven J. Shin-Sim, Myung Morton, Donald L. Faries, Mark B. Sieling, Peter A. Lee, Delphine J. Front Oncol Oncology Stage IV metastatic melanoma patients historically have a poor prognosis with 5–10% 5-year survival. Ipilimumab, a monoclonal antibody against cytotoxic T-lymphocyte antigen 4 (CTLA4), is one of the first treatments to provide beneficial durable responses in advanced melanoma. However, less than 25% of those treated benefit, treatment is expensive, and side effects can be fatal. Since soluble (s) CTLA4 may mediate inhibitory effects previously ascribed to the membrane-bound isoform (mCTLA4), we hypothesized patients benefiting from ipilimumab have higher serum levels of sCTLA4. We found that higher sCTLA4 levels correlated both with response and improved survival in patients treated with ipilimumab in a small patient cohort [patients with (n = 9) and without (n = 5) clinical benefit]. sCTLA4 levels were statistically higher in ipilimumab-treated patients with response to ipilimumab. In contrast, sCTLA4 levels did not correlate with survival in patients who did not receive ipilimumab (n = 11). These preliminary observations provide a previously unrecognized link between serum sCTLA4 levels and response to ipilimumab as well as to improved survival in ipilimumab-treated melanoma patients and a potential mechanism by which ipilimumab functions. Frontiers Media S.A. 2014-05-16 /pmc/articles/PMC4032905/ /pubmed/24904825 http://dx.doi.org/10.3389/fonc.2014.00110 Text en Copyright © 2014 Leung, Lee, Ozao-Choy, Ramos, Hamid, O’Day, Shin-Sim, Morton, Faries, Sieling and Lee. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Leung, Anna M. Lee, Agnes Fermin Ozao-Choy, Junko Ramos, Romela Irene Hamid, Omid O’Day, Steven J. Shin-Sim, Myung Morton, Donald L. Faries, Mark B. Sieling, Peter A. Lee, Delphine J. Clinical Benefit from Ipilimumab Therapy in Melanoma Patients may be Associated with Serum CTLA4 Levels |
title | Clinical Benefit from Ipilimumab Therapy in Melanoma Patients may be Associated with Serum CTLA4 Levels |
title_full | Clinical Benefit from Ipilimumab Therapy in Melanoma Patients may be Associated with Serum CTLA4 Levels |
title_fullStr | Clinical Benefit from Ipilimumab Therapy in Melanoma Patients may be Associated with Serum CTLA4 Levels |
title_full_unstemmed | Clinical Benefit from Ipilimumab Therapy in Melanoma Patients may be Associated with Serum CTLA4 Levels |
title_short | Clinical Benefit from Ipilimumab Therapy in Melanoma Patients may be Associated with Serum CTLA4 Levels |
title_sort | clinical benefit from ipilimumab therapy in melanoma patients may be associated with serum ctla4 levels |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032905/ https://www.ncbi.nlm.nih.gov/pubmed/24904825 http://dx.doi.org/10.3389/fonc.2014.00110 |
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