| Literature DB >> 30131322 |
Emilie Soularue1,2, Patricia Lepage3, Caroline Robert2,4, Franck Carbonnel1,2, Jean Frederic Colombel5, Clelia Coutzac6, David Faleck5, Lysiane Marthey1, Michael Collins1,2, Nathalie Chaput6,7.
Abstract
Immune checkpoint inhibitors targeting cytotoxic T-lymphocyte-associated protein-4 (CTLA-4) and programmed death-1 (PD-1)/ligand are increasingly used to treat several types of cancer. These drugs enhance antitumour T-cell activity and therefore induce immune-related adverse effects (irAE), of which gastrointestinal (GI) irAE are among the most frequent and severe. This systematic literature review summarises the clinical manifestations, management and pathophysiology of GI irAE due to immune checkpoint inhibitors. GI irAE induced by anti-CTLA-4 are frequent, potentially severe and resemble IBD, whereas those induced by PD-1 blockade seem to be less frequent and clinically more diverse. Baseline symbiotic gut microbiota is associated with an enhanced antitumour response to immune checkpoint inhibitors and an increased susceptibility to developing enterocolitis, in patients treated with anti-CTLA-4. These findings open new perspectives for possible manipulation of the gut microbiota in order to better identify responders to immune checkpoint inhibitors and to increase their efficacy and safety. © Author(s) (or their employer(s)) 2018. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: colonic microflora; immunotherapy; inflammatory bowel disease
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Year: 2018 PMID: 30131322 DOI: 10.1136/gutjnl-2018-316948
Source DB: PubMed Journal: Gut ISSN: 0017-5749 Impact factor: 23.059