Pembrolizumab for the treatment of uveal melanoma: A case series

Uveal melanoma is a rare disease. Up to 50% of the patients will develop metastases for which the treatment options are limited. No randomized controlled data for the treatment of uveal melanoma patients are available. In this study we describe the clinical course of nine uveal melanoma patients inc...

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Main Authors: Yanina Jeanne Leona Jansen, Teofila Seremet, Bart Neyns
Format: Article
Language:English
Published: SAGE Publishing 2020-11-01
Series:Rare Tumors
Online Access:https://doi.org/10.1177/2036361320971983
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spelling doaj-52873ce27c474fb2aaf32b41fbd02da62020-11-25T04:07:00ZengSAGE PublishingRare Tumors2036-36132020-11-011210.1177/2036361320971983Pembrolizumab for the treatment of uveal melanoma: A case seriesYanina Jeanne Leona Jansen0Teofila Seremet1Bart Neyns2Department of Medical Oncology, Universitair Ziekenhuis Brussel, Vrije Universiteit Brussel, Brussels, BelgiumDermatology, CHUV Lausanne university hospital, Lausanne, SwitzerlandDepartment of Medical Oncology, Universitair Ziekenhuis Brussel, Vrije Universiteit Brussel, Brussels, BelgiumUveal melanoma is a rare disease. Up to 50% of the patients will develop metastases for which the treatment options are limited. No randomized controlled data for the treatment of uveal melanoma patients are available. In this study we describe the clinical course of nine uveal melanoma patients included in the pembrolizumab expanded access program (EAP) in Belgium. Nine uveal melanoma patients were treated in the EAP with 2mg/kg pembrolizumab every 3 weeks. Patients received pembrolizumab as first or second-line treatment. Baseline characteristics and tumor responses were prospectively collected. During a median follow-up of 40 weeks, the estimated median PFS was 18 weeks (95% CI 0.7–35) and median OS was 46 weeks (95% CI 33–59%). Four patients had stable disease (SD) for more than 20 weeks (PFS of 21, 22, and 27 weeks respectively) and 1 patient presented with SD for 119 weeks. No objective responses according to irRC were observed. One grade 3 hepatitis occurred which was reversible with the administration of high doses oral corticosteroids. Even though treatment with pembrolizumab is well tolerated, clinical benefit is disappointing. Nevertheless long-term diseases control can be achieved in selected caseshttps://doi.org/10.1177/2036361320971983
collection DOAJ
language English
format Article
sources DOAJ
author Yanina Jeanne Leona Jansen
Teofila Seremet
Bart Neyns
spellingShingle Yanina Jeanne Leona Jansen
Teofila Seremet
Bart Neyns
Pembrolizumab for the treatment of uveal melanoma: A case series
Rare Tumors
author_facet Yanina Jeanne Leona Jansen
Teofila Seremet
Bart Neyns
author_sort Yanina Jeanne Leona Jansen
title Pembrolizumab for the treatment of uveal melanoma: A case series
title_short Pembrolizumab for the treatment of uveal melanoma: A case series
title_full Pembrolizumab for the treatment of uveal melanoma: A case series
title_fullStr Pembrolizumab for the treatment of uveal melanoma: A case series
title_full_unstemmed Pembrolizumab for the treatment of uveal melanoma: A case series
title_sort pembrolizumab for the treatment of uveal melanoma: a case series
publisher SAGE Publishing
series Rare Tumors
issn 2036-3613
publishDate 2020-11-01
description Uveal melanoma is a rare disease. Up to 50% of the patients will develop metastases for which the treatment options are limited. No randomized controlled data for the treatment of uveal melanoma patients are available. In this study we describe the clinical course of nine uveal melanoma patients included in the pembrolizumab expanded access program (EAP) in Belgium. Nine uveal melanoma patients were treated in the EAP with 2mg/kg pembrolizumab every 3 weeks. Patients received pembrolizumab as first or second-line treatment. Baseline characteristics and tumor responses were prospectively collected. During a median follow-up of 40 weeks, the estimated median PFS was 18 weeks (95% CI 0.7–35) and median OS was 46 weeks (95% CI 33–59%). Four patients had stable disease (SD) for more than 20 weeks (PFS of 21, 22, and 27 weeks respectively) and 1 patient presented with SD for 119 weeks. No objective responses according to irRC were observed. One grade 3 hepatitis occurred which was reversible with the administration of high doses oral corticosteroids. Even though treatment with pembrolizumab is well tolerated, clinical benefit is disappointing. Nevertheless long-term diseases control can be achieved in selected cases
url https://doi.org/10.1177/2036361320971983
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