| Literature DB >> 30190821 |
Peter Hersey1,2,1,2, Hojabr Kakavand2,3,2,3, James Wilmott2,3,2,3, Andre van der Westhuizen4,4, Stuart Gallagher1,1, Kavitha Gowrishankar1,1, Richard Scolyer2,3,2,3.
Abstract
The introduction of immunotherapy based on the blockade of the PD1/PD-L1 checkpoints has been associated with high response rates and durable remissions of disease in patients with metastatic melanoma, to the extent that it is now considered the standard of care for a wide range of patients, irrespective of their BRAF or NRAS mutation status. In addition, more frequent follow-up of patients who are at high risk of recurrence after surgical treatment appears to be justified, as does neoadjuvant treatments in order to render patients treatable by surgery. The limitations of this treatment include failure of some patients to respond, a low rate of complete responses and relapses of the disease during treatment. New initiatives in order to overcome these limitations include the identification of biomarkers for the selection responders and evaluations of treatment combinations that will increase responses and their durability. The latter includes combinations with antibodies against other checkpoints on T cells and cotreatments with inhibitors of resistance pathways in melanoma.Entities:
Keywords: CD8 T cells; PD1/PD-L1; TILs; immunotherapy; melanoma; monoclonal antibodies; resistance factors; survival outcomes
Year: 2014 PMID: 30190821 PMCID: PMC6094707 DOI: 10.2217/mmt.14.14
Source DB: PubMed Journal: Melanoma Manag ISSN: 2045-0885