Broeckelmann, Paul J. and Engert, Andreas (2017). Checkpoint Inhibition in Hodgkin Lymphoma - a Review. Oncol. Res. Treat., 40 (11). S. 654 - 660. BASEL: KARGER. ISSN 2296-5262

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Abstract

Physiological immune checkpoint pathways are important to regulate self-tolerance, limit immune reactions, and moderate autoimmunity. Various cancers are commonly exploiting these mechanisms to evade the host immune system by restraining a durable, efficient antitumor immune response. Immune checkpoints include, but are not limited to, the programmed death 1 (PD1) and the cytotoxic T-lymphocyte-associated protein-4 (CTLA4) axis, which are both druggable by monoclonal antibodies referred to as checkpoint inhibitors (CIs). To date, the anti-PD1 antibodies nivolumab and pembrolizumab are approved for relapsed or refractory classical Hodgkin lymphoma (cHL) due to high response rates with a favorable yet distinct safety profile, and other agents are under investigation. This review summarizes the available preclinical and clinical data including the toxicity and efficacy of different CIs in cHL. It also provides future perspectives based on ongoing clinical trials, potentially synergistic combinatory approaches, and their fit in the therapeutic landscape in cHL. (C) 2017 S. Karger GmbH, Freiburg

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Broeckelmann, Paul J.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Engert, AndreasUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-213649
DOI: 10.1159/000481800
Journal or Publication Title: Oncol. Res. Treat.
Volume: 40
Number: 11
Page Range: S. 654 - 660
Date: 2017
Publisher: KARGER
Place of Publication: BASEL
ISSN: 2296-5262
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
BRENTUXIMAB VEDOTIN; PD-1 BLOCKADE; PHASE-II; EXPRESSION; IPILIMUMAB; NIVOLUMAB; CANCER; MICROENVIRONMENT; PEMBROLIZUMAB; CHEMOTHERAPYMultiple languages
OncologyMultiple languages
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/21364

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