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Anti‐PD‐1 antibodies in metastatic uveal melanoma: a treatment option?

Uveal melanomas (UMs) are a rare form of cancer with clinical and pathological characteristics distinct from cutaneous melanomas. Ipilimumab has shown efficacy and safety in the treatment of metastatic UM. This provides a rationale for treatment with other immune checkpoint inhibitors. This is a ret...

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Autores principales: Bender, Carolin, Enk, Alexander, Gutzmer, Ralf, Hassel, Jessica C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504332/
https://www.ncbi.nlm.nih.gov/pubmed/28639409
http://dx.doi.org/10.1002/cam4.887
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author Bender, Carolin
Enk, Alexander
Gutzmer, Ralf
Hassel, Jessica C.
author_facet Bender, Carolin
Enk, Alexander
Gutzmer, Ralf
Hassel, Jessica C.
author_sort Bender, Carolin
collection PubMed
description Uveal melanomas (UMs) are a rare form of cancer with clinical and pathological characteristics distinct from cutaneous melanomas. Ipilimumab has shown efficacy and safety in the treatment of metastatic UM. This provides a rationale for treatment with other immune checkpoint inhibitors. This is a retrospective review of 15 patients with metastatic UM treated between June 2014 and February 2016, who received treatment with the anti‐PD‐1 Abs pembrolizumab or nivolumab. Patients were treated at two German university hospitals. Therapy was administered at the approved dosing schedules of 2 mg/kg q3w for pembrolizumab and 3 mg/kg q2w for nivolumab. Treatment was given until first tumor assessment and continued if tumor assessment showed disease control. Tumor assessments were performed at baseline and following scans every 12 weeks. Patients were monitored throughout for adverse events. Best response to treatment was stable disease in four patients. Eight out of 15 (53%) patients received treatment until first tumor assessment. As of February 2016, median progression‐free survival (PFS) is 3 months (range 0.75–6.75 months) and overall survival (OS) is 5 months (range 1–16 months). Eight out of 15 (53%) patients are still alive (two patients lost to follow‐up) with one out of four patients is in ongoing disease control. Patients with multiple organ metastases and elevated serum lactate dehydrogenase did not respond well to treatment. No objective response to PD‐1 Ab therapy was seen. Best response to treatment was stable disease in four patients. Treatment was well tolerated with manageable toxicity.
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spelling pubmed-55043322017-07-12 Anti‐PD‐1 antibodies in metastatic uveal melanoma: a treatment option? Bender, Carolin Enk, Alexander Gutzmer, Ralf Hassel, Jessica C. Cancer Med Clinical Cancer Research Uveal melanomas (UMs) are a rare form of cancer with clinical and pathological characteristics distinct from cutaneous melanomas. Ipilimumab has shown efficacy and safety in the treatment of metastatic UM. This provides a rationale for treatment with other immune checkpoint inhibitors. This is a retrospective review of 15 patients with metastatic UM treated between June 2014 and February 2016, who received treatment with the anti‐PD‐1 Abs pembrolizumab or nivolumab. Patients were treated at two German university hospitals. Therapy was administered at the approved dosing schedules of 2 mg/kg q3w for pembrolizumab and 3 mg/kg q2w for nivolumab. Treatment was given until first tumor assessment and continued if tumor assessment showed disease control. Tumor assessments were performed at baseline and following scans every 12 weeks. Patients were monitored throughout for adverse events. Best response to treatment was stable disease in four patients. Eight out of 15 (53%) patients received treatment until first tumor assessment. As of February 2016, median progression‐free survival (PFS) is 3 months (range 0.75–6.75 months) and overall survival (OS) is 5 months (range 1–16 months). Eight out of 15 (53%) patients are still alive (two patients lost to follow‐up) with one out of four patients is in ongoing disease control. Patients with multiple organ metastases and elevated serum lactate dehydrogenase did not respond well to treatment. No objective response to PD‐1 Ab therapy was seen. Best response to treatment was stable disease in four patients. Treatment was well tolerated with manageable toxicity. John Wiley and Sons Inc. 2017-06-21 /pmc/articles/PMC5504332/ /pubmed/28639409 http://dx.doi.org/10.1002/cam4.887 Text en © 2017 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Bender, Carolin
Enk, Alexander
Gutzmer, Ralf
Hassel, Jessica C.
Anti‐PD‐1 antibodies in metastatic uveal melanoma: a treatment option?
title Anti‐PD‐1 antibodies in metastatic uveal melanoma: a treatment option?
title_full Anti‐PD‐1 antibodies in metastatic uveal melanoma: a treatment option?
title_fullStr Anti‐PD‐1 antibodies in metastatic uveal melanoma: a treatment option?
title_full_unstemmed Anti‐PD‐1 antibodies in metastatic uveal melanoma: a treatment option?
title_short Anti‐PD‐1 antibodies in metastatic uveal melanoma: a treatment option?
title_sort anti‐pd‐1 antibodies in metastatic uveal melanoma: a treatment option?
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504332/
https://www.ncbi.nlm.nih.gov/pubmed/28639409
http://dx.doi.org/10.1002/cam4.887
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