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Treatment with Ipilimumab: A Case Report of Complete Response in a Metastatic Malignant Melanoma Patient

INTRODUCTION: Over the past year, 3 agents have been approved for the treatment of melanoma by the Food and Drug Administration. These include pegylated interferon α-2b for stage III melanoma, vemurafenib for unresectable or metastatic melanoma with BRAF V600E mutation, and ipilimumab for unresectab...

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Autores principales: Addeo, Alfredo, Rinaldi, Ciro Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3725017/
https://www.ncbi.nlm.nih.gov/pubmed/23898270
http://dx.doi.org/10.1159/000351834
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author Addeo, Alfredo
Rinaldi, Ciro Roberto
author_facet Addeo, Alfredo
Rinaldi, Ciro Roberto
author_sort Addeo, Alfredo
collection PubMed
description INTRODUCTION: Over the past year, 3 agents have been approved for the treatment of melanoma by the Food and Drug Administration. These include pegylated interferon α-2b for stage III melanoma, vemurafenib for unresectable or metastatic melanoma with BRAF V600E mutation, and ipilimumab for unresectable or metastatic melanoma. CASE PRESENTATION: We present here the case of a 65-year-old Caucasian male diagnosed with advanced melanoma in April 2011 and treated with ipilimumab (Yervoy(®)), a monoclonal antibody targeting cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), as second-line treatment after progression with dacarbazine, for (wild-type BRAF) metastatic melanoma. The patient was referred to us for several painful lumps on his right arm. A biopsy of one of them revealed melanoma. CT and PET scans did not show any other lesions or a primary site. The patient was started on first-line chemotherapy with dacarbazine 850 mg/m(2) on day 1, every 3 weeks. After 3 cycles, the patient showed disease progression with an increase in size of the skin metastasis. Second-line treatment was started with ipilimumab 3 mg/kg on day 1, every 3 weeks. At the end of the treatment, after 4 cycles, we documented a complete clinical response with total resolution of the skin metastasis. At the time of writing this paper, our patient had finished his treatment more than 9 months earlier and is still in complete remission. CONCLUSION: This is a paradigmatic case where, despite extensive metastatic disease, treatment with ipilimumab has confirmed its efficacy. It is still an open question why only a minority of patients have such a remarkable response, and further trials are warranted to address this important question.
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spelling pubmed-37250172013-07-29 Treatment with Ipilimumab: A Case Report of Complete Response in a Metastatic Malignant Melanoma Patient Addeo, Alfredo Rinaldi, Ciro Roberto Case Rep Oncol Published online: May, 2013 INTRODUCTION: Over the past year, 3 agents have been approved for the treatment of melanoma by the Food and Drug Administration. These include pegylated interferon α-2b for stage III melanoma, vemurafenib for unresectable or metastatic melanoma with BRAF V600E mutation, and ipilimumab for unresectable or metastatic melanoma. CASE PRESENTATION: We present here the case of a 65-year-old Caucasian male diagnosed with advanced melanoma in April 2011 and treated with ipilimumab (Yervoy(®)), a monoclonal antibody targeting cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), as second-line treatment after progression with dacarbazine, for (wild-type BRAF) metastatic melanoma. The patient was referred to us for several painful lumps on his right arm. A biopsy of one of them revealed melanoma. CT and PET scans did not show any other lesions or a primary site. The patient was started on first-line chemotherapy with dacarbazine 850 mg/m(2) on day 1, every 3 weeks. After 3 cycles, the patient showed disease progression with an increase in size of the skin metastasis. Second-line treatment was started with ipilimumab 3 mg/kg on day 1, every 3 weeks. At the end of the treatment, after 4 cycles, we documented a complete clinical response with total resolution of the skin metastasis. At the time of writing this paper, our patient had finished his treatment more than 9 months earlier and is still in complete remission. CONCLUSION: This is a paradigmatic case where, despite extensive metastatic disease, treatment with ipilimumab has confirmed its efficacy. It is still an open question why only a minority of patients have such a remarkable response, and further trials are warranted to address this important question. S. Karger AG 2013-05-30 /pmc/articles/PMC3725017/ /pubmed/23898270 http://dx.doi.org/10.1159/000351834 Text en Copyright © 2013 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Users may download, print and share this work on the Internet for noncommercial purposes only, provided the original work is properly cited, and a link to the original work on http://www.karger.com and the terms of this license are included in any shared versions.
spellingShingle Published online: May, 2013
Addeo, Alfredo
Rinaldi, Ciro Roberto
Treatment with Ipilimumab: A Case Report of Complete Response in a Metastatic Malignant Melanoma Patient
title Treatment with Ipilimumab: A Case Report of Complete Response in a Metastatic Malignant Melanoma Patient
title_full Treatment with Ipilimumab: A Case Report of Complete Response in a Metastatic Malignant Melanoma Patient
title_fullStr Treatment with Ipilimumab: A Case Report of Complete Response in a Metastatic Malignant Melanoma Patient
title_full_unstemmed Treatment with Ipilimumab: A Case Report of Complete Response in a Metastatic Malignant Melanoma Patient
title_short Treatment with Ipilimumab: A Case Report of Complete Response in a Metastatic Malignant Melanoma Patient
title_sort treatment with ipilimumab: a case report of complete response in a metastatic malignant melanoma patient
topic Published online: May, 2013
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3725017/
https://www.ncbi.nlm.nih.gov/pubmed/23898270
http://dx.doi.org/10.1159/000351834
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