Emerging treatment options for the management of Hodgkin's lymphoma: clinical utility of Nivolumab

David A Bond, Lapo Alinari Department of Internal Medicine, Division of Hematology, Arthur G James Comprehensive Cancer Center, The Ohio State University Wexner Medical Center, Columbus, OH, USA Abstract: Classical Hodgkin’s lymphoma (cHL) is a B-cell malignancy comprised of patho...

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Main Authors: Bond DA, Alinari L
Format: Article
Language:English
Published: Dove Medical Press 2017-05-01
Series:Journal of Blood Medicine
Subjects:
Online Access:https://www.dovepress.com/emerging-treatment-options-for-the-management-of-hodgkins-lymphoma-cl-peer-reviewed-article-JBM
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spelling doaj-775a214d048945a3a60ff7a0c86e05002020-11-25T00:10:16ZengDove Medical PressJournal of Blood Medicine1179-27362017-05-01Volume 8415432797Emerging treatment options for the management of Hodgkin's lymphoma: clinical utility of NivolumabBond DAAlinari LDavid A Bond, Lapo Alinari Department of Internal Medicine, Division of Hematology, Arthur G James Comprehensive Cancer Center, The Ohio State University Wexner Medical Center, Columbus, OH, USA Abstract: Classical Hodgkin’s lymphoma (cHL) is a B-cell malignancy comprised of pathologic Reed Sternberg cells with a surrounding immune-tolerant inflammatory milieu. RS cells evade immune recognition in part through programmed death ligand 1 (PD-L1) overexpression, which is genetically programmed through copy number alterations, polysomy, and amplification of the 9p24.1 locus encoding PD-L1. By engaging with PD-1+ T-cells, PD-L1 delivers a potent immune suppressive signal promoting immunologic escape of the tumor cell. Enhancing antitumor immune response by targeting PD-1 with the monoclonal antibody nivolumab has proved to be effective in multiple solid tumors, but the highest response rates to date have been reported in patients with cHL, with over 65% of treated patients achieving an objective clinical response. In this review, we will summarize the published evidence regarding the activity of nivolumab in cHL as well as its current place in therapy. We will review the pharmacology, mechanism of action, and side effects of nivolumab as well as the emerging data indicating possible increased risk of graft versus host disease in patients treated with PD-1 inhibitors either pre- or post-allogeneic stem cell transplant. Given the remarkable single-agent activity and safety profile of PD-1 inhibitors in heavily pretreated patients with cHL, the possibility of employing nivolumab in combination with other active agents and earlier in therapy is a promising area of active investigation, and we will briefly summarize current clinical trials. Keywords: nivolumab, Hodgkin’s lymphoma, pembrolizumab, checkpoint inhibitor therapyhttps://www.dovepress.com/emerging-treatment-options-for-the-management-of-hodgkins-lymphoma-cl-peer-reviewed-article-JBMnivolumab Hodgkins lymphoma pembrolizumab checkpoint inhibitor therapy
collection DOAJ
language English
format Article
sources DOAJ
author Bond DA
Alinari L
spellingShingle Bond DA
Alinari L
Emerging treatment options for the management of Hodgkin's lymphoma: clinical utility of Nivolumab
Journal of Blood Medicine
nivolumab Hodgkins lymphoma pembrolizumab checkpoint inhibitor therapy
author_facet Bond DA
Alinari L
author_sort Bond DA
title Emerging treatment options for the management of Hodgkin's lymphoma: clinical utility of Nivolumab
title_short Emerging treatment options for the management of Hodgkin's lymphoma: clinical utility of Nivolumab
title_full Emerging treatment options for the management of Hodgkin's lymphoma: clinical utility of Nivolumab
title_fullStr Emerging treatment options for the management of Hodgkin's lymphoma: clinical utility of Nivolumab
title_full_unstemmed Emerging treatment options for the management of Hodgkin's lymphoma: clinical utility of Nivolumab
title_sort emerging treatment options for the management of hodgkin's lymphoma: clinical utility of nivolumab
publisher Dove Medical Press
series Journal of Blood Medicine
issn 1179-2736
publishDate 2017-05-01
description David A Bond, Lapo Alinari Department of Internal Medicine, Division of Hematology, Arthur G James Comprehensive Cancer Center, The Ohio State University Wexner Medical Center, Columbus, OH, USA Abstract: Classical Hodgkin’s lymphoma (cHL) is a B-cell malignancy comprised of pathologic Reed Sternberg cells with a surrounding immune-tolerant inflammatory milieu. RS cells evade immune recognition in part through programmed death ligand 1 (PD-L1) overexpression, which is genetically programmed through copy number alterations, polysomy, and amplification of the 9p24.1 locus encoding PD-L1. By engaging with PD-1+ T-cells, PD-L1 delivers a potent immune suppressive signal promoting immunologic escape of the tumor cell. Enhancing antitumor immune response by targeting PD-1 with the monoclonal antibody nivolumab has proved to be effective in multiple solid tumors, but the highest response rates to date have been reported in patients with cHL, with over 65% of treated patients achieving an objective clinical response. In this review, we will summarize the published evidence regarding the activity of nivolumab in cHL as well as its current place in therapy. We will review the pharmacology, mechanism of action, and side effects of nivolumab as well as the emerging data indicating possible increased risk of graft versus host disease in patients treated with PD-1 inhibitors either pre- or post-allogeneic stem cell transplant. Given the remarkable single-agent activity and safety profile of PD-1 inhibitors in heavily pretreated patients with cHL, the possibility of employing nivolumab in combination with other active agents and earlier in therapy is a promising area of active investigation, and we will briefly summarize current clinical trials. Keywords: nivolumab, Hodgkin’s lymphoma, pembrolizumab, checkpoint inhibitor therapy
topic nivolumab Hodgkins lymphoma pembrolizumab checkpoint inhibitor therapy
url https://www.dovepress.com/emerging-treatment-options-for-the-management-of-hodgkins-lymphoma-cl-peer-reviewed-article-JBM
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