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The Price of Tumor Control: An Analysis of Rare Side Effects of Anti-CTLA-4 Therapy in Metastatic Melanoma from the Ipilimumab Network

BACKGROUND: Ipilimumab, a cytotoxic T-lymphocyte antigen-4 (CTLA-4) blocking antibody, has been approved for the treatment of metastatic melanoma and induces adverse events (AE) in up to 64% of patients. Treatment algorithms for the management of common ipilimumab-induced AEs have lead to a reductio...

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Autores principales: Voskens, Caroline J., Goldinger, Simone M., Loquai, Carmen, Robert, Caroline, Kaehler, Katharina C., Berking, Carola, Bergmann, Tanja, Bockmeyer, Clemens L., Eigentler, Thomas, Fluck, Michael, Garbe, Claus, Gutzmer, Ralf, Grabbe, Stephan, Hauschild, Axel, Hein, Rüdiger, Hundorfean, Gheorghe, Justich, Armin, Keller, Ullrich, Klein, Christina, Mateus, Christine, Mohr, Peter, Paetzold, Sylvie, Satzger, Imke, Schadendorf, Dirk, Schlaeppi, Marc, Schuler, Gerold, Schuler-Thurner, Beatrice, Trefzer, Uwe, Ulrich, Jens, Vaubel, Julia, von Moos, Roger, Weder, Patrik, Wilhelm, Tabea, Göppner, Daniela, Dummer, Reinhard, Heinzerling, Lucie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544906/
https://www.ncbi.nlm.nih.gov/pubmed/23341990
http://dx.doi.org/10.1371/journal.pone.0053745
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author Voskens, Caroline J.
Goldinger, Simone M.
Loquai, Carmen
Robert, Caroline
Kaehler, Katharina C.
Berking, Carola
Bergmann, Tanja
Bockmeyer, Clemens L.
Eigentler, Thomas
Fluck, Michael
Garbe, Claus
Gutzmer, Ralf
Grabbe, Stephan
Hauschild, Axel
Hein, Rüdiger
Hundorfean, Gheorghe
Justich, Armin
Keller, Ullrich
Klein, Christina
Mateus, Christine
Mohr, Peter
Paetzold, Sylvie
Satzger, Imke
Schadendorf, Dirk
Schlaeppi, Marc
Schuler, Gerold
Schuler-Thurner, Beatrice
Trefzer, Uwe
Ulrich, Jens
Vaubel, Julia
von Moos, Roger
Weder, Patrik
Wilhelm, Tabea
Göppner, Daniela
Dummer, Reinhard
Heinzerling, Lucie M.
author_facet Voskens, Caroline J.
Goldinger, Simone M.
Loquai, Carmen
Robert, Caroline
Kaehler, Katharina C.
Berking, Carola
Bergmann, Tanja
Bockmeyer, Clemens L.
Eigentler, Thomas
Fluck, Michael
Garbe, Claus
Gutzmer, Ralf
Grabbe, Stephan
Hauschild, Axel
Hein, Rüdiger
Hundorfean, Gheorghe
Justich, Armin
Keller, Ullrich
Klein, Christina
Mateus, Christine
Mohr, Peter
Paetzold, Sylvie
Satzger, Imke
Schadendorf, Dirk
Schlaeppi, Marc
Schuler, Gerold
Schuler-Thurner, Beatrice
Trefzer, Uwe
Ulrich, Jens
Vaubel, Julia
von Moos, Roger
Weder, Patrik
Wilhelm, Tabea
Göppner, Daniela
Dummer, Reinhard
Heinzerling, Lucie M.
author_sort Voskens, Caroline J.
collection PubMed
description BACKGROUND: Ipilimumab, a cytotoxic T-lymphocyte antigen-4 (CTLA-4) blocking antibody, has been approved for the treatment of metastatic melanoma and induces adverse events (AE) in up to 64% of patients. Treatment algorithms for the management of common ipilimumab-induced AEs have lead to a reduction of morbidity, e.g. due to bowel perforations. However, the spectrum of less common AEs is expanding as ipilimumab is increasingly applied. Stringent recognition and management of AEs will reduce drug-induced morbidity and costs, and thus, positively impact the cost-benefit ratio of the drug. To facilitate timely identification and adequate management data on rare AEs were analyzed at 19 skin cancer centers. METHODS AND FINDINGS: Patient files (n = 752) were screened for rare ipilimumab-associated AEs. A total of 120 AEs, some of which were life-threatening or even fatal, were reported and summarized by organ system describing the most instructive cases in detail. Previously unreported AEs like drug rash with eosinophilia and systemic symptoms (DRESS), granulomatous inflammation of the central nervous system, and aseptic meningitis, were documented. Obstacles included patientś delay in reporting symptoms and the differentiation of steroid-induced from ipilimumab-induced AEs under steroid treatment. Importantly, response rate was high in this patient population with tumor regression in 30.9% and a tumor control rate of 61.8% in stage IV melanoma patients despite the fact that some patients received only two of four recommended ipilimumab infusions. This suggests that ipilimumab-induced antitumor responses can have an early onset and that severe autoimmune reactions may reflect overtreatment. CONCLUSION: The wide spectrum of ipilimumab-induced AEs demands doctor and patient awareness to reduce morbidity and treatment costs and true ipilimumab success is dictated by both objective tumor responses and controlling severe side effects.
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spelling pubmed-35449062013-01-22 The Price of Tumor Control: An Analysis of Rare Side Effects of Anti-CTLA-4 Therapy in Metastatic Melanoma from the Ipilimumab Network Voskens, Caroline J. Goldinger, Simone M. Loquai, Carmen Robert, Caroline Kaehler, Katharina C. Berking, Carola Bergmann, Tanja Bockmeyer, Clemens L. Eigentler, Thomas Fluck, Michael Garbe, Claus Gutzmer, Ralf Grabbe, Stephan Hauschild, Axel Hein, Rüdiger Hundorfean, Gheorghe Justich, Armin Keller, Ullrich Klein, Christina Mateus, Christine Mohr, Peter Paetzold, Sylvie Satzger, Imke Schadendorf, Dirk Schlaeppi, Marc Schuler, Gerold Schuler-Thurner, Beatrice Trefzer, Uwe Ulrich, Jens Vaubel, Julia von Moos, Roger Weder, Patrik Wilhelm, Tabea Göppner, Daniela Dummer, Reinhard Heinzerling, Lucie M. PLoS One Research Article BACKGROUND: Ipilimumab, a cytotoxic T-lymphocyte antigen-4 (CTLA-4) blocking antibody, has been approved for the treatment of metastatic melanoma and induces adverse events (AE) in up to 64% of patients. Treatment algorithms for the management of common ipilimumab-induced AEs have lead to a reduction of morbidity, e.g. due to bowel perforations. However, the spectrum of less common AEs is expanding as ipilimumab is increasingly applied. Stringent recognition and management of AEs will reduce drug-induced morbidity and costs, and thus, positively impact the cost-benefit ratio of the drug. To facilitate timely identification and adequate management data on rare AEs were analyzed at 19 skin cancer centers. METHODS AND FINDINGS: Patient files (n = 752) were screened for rare ipilimumab-associated AEs. A total of 120 AEs, some of which were life-threatening or even fatal, were reported and summarized by organ system describing the most instructive cases in detail. Previously unreported AEs like drug rash with eosinophilia and systemic symptoms (DRESS), granulomatous inflammation of the central nervous system, and aseptic meningitis, were documented. Obstacles included patientś delay in reporting symptoms and the differentiation of steroid-induced from ipilimumab-induced AEs under steroid treatment. Importantly, response rate was high in this patient population with tumor regression in 30.9% and a tumor control rate of 61.8% in stage IV melanoma patients despite the fact that some patients received only two of four recommended ipilimumab infusions. This suggests that ipilimumab-induced antitumor responses can have an early onset and that severe autoimmune reactions may reflect overtreatment. CONCLUSION: The wide spectrum of ipilimumab-induced AEs demands doctor and patient awareness to reduce morbidity and treatment costs and true ipilimumab success is dictated by both objective tumor responses and controlling severe side effects. Public Library of Science 2013-01-14 /pmc/articles/PMC3544906/ /pubmed/23341990 http://dx.doi.org/10.1371/journal.pone.0053745 Text en © 2013 Voskens et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Voskens, Caroline J.
Goldinger, Simone M.
Loquai, Carmen
Robert, Caroline
Kaehler, Katharina C.
Berking, Carola
Bergmann, Tanja
Bockmeyer, Clemens L.
Eigentler, Thomas
Fluck, Michael
Garbe, Claus
Gutzmer, Ralf
Grabbe, Stephan
Hauschild, Axel
Hein, Rüdiger
Hundorfean, Gheorghe
Justich, Armin
Keller, Ullrich
Klein, Christina
Mateus, Christine
Mohr, Peter
Paetzold, Sylvie
Satzger, Imke
Schadendorf, Dirk
Schlaeppi, Marc
Schuler, Gerold
Schuler-Thurner, Beatrice
Trefzer, Uwe
Ulrich, Jens
Vaubel, Julia
von Moos, Roger
Weder, Patrik
Wilhelm, Tabea
Göppner, Daniela
Dummer, Reinhard
Heinzerling, Lucie M.
The Price of Tumor Control: An Analysis of Rare Side Effects of Anti-CTLA-4 Therapy in Metastatic Melanoma from the Ipilimumab Network
title The Price of Tumor Control: An Analysis of Rare Side Effects of Anti-CTLA-4 Therapy in Metastatic Melanoma from the Ipilimumab Network
title_full The Price of Tumor Control: An Analysis of Rare Side Effects of Anti-CTLA-4 Therapy in Metastatic Melanoma from the Ipilimumab Network
title_fullStr The Price of Tumor Control: An Analysis of Rare Side Effects of Anti-CTLA-4 Therapy in Metastatic Melanoma from the Ipilimumab Network
title_full_unstemmed The Price of Tumor Control: An Analysis of Rare Side Effects of Anti-CTLA-4 Therapy in Metastatic Melanoma from the Ipilimumab Network
title_short The Price of Tumor Control: An Analysis of Rare Side Effects of Anti-CTLA-4 Therapy in Metastatic Melanoma from the Ipilimumab Network
title_sort price of tumor control: an analysis of rare side effects of anti-ctla-4 therapy in metastatic melanoma from the ipilimumab network
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3544906/
https://www.ncbi.nlm.nih.gov/pubmed/23341990
http://dx.doi.org/10.1371/journal.pone.0053745
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