| Literature DB >> 26829031 |
Nicolas Jacquelot1, María Paula Roberti2, David P Enot3, Sylvie Rusakiewicz2, Michaela Semeraro4, Sarah Jégou5, Camila Flores6, Lieping Chen7, Byoung S Kwon8, Christophe Borg9, Benjamin Weide10, François Aubin11, Stéphane Dalle12, Holbrook Kohrt13, Maha Ayyoub14, Guido Kroemer15, Aurélien Marabelle2, Andréa Cavalcanti16, Alexander Eggermont6, Laurence Zitvogel17.
Abstract
Stage III metastatic melanomas require adequate adjuvant immunotherapy to prevent relapses. Prognostic factors are awaited to optimize the clinical management of these patients. The magnitude of metastatic lymph node invasion and the BRAF(V600) activating mutation have clinical significance. Based on a comprehensive immunophenotyping of 252 parameters per patient in paired blood and metastatic lymph nodes performed in 39 metastatic melanomas, we found that blood markers were as contributive as tumor-infiltrated lymphocyte immunotypes, and parameters associated with lymphocyte exhaustion/suppression showed higher clinical significance than those related to activation or lineage. High frequencies of CD45RA(+)CD4(+) and CD3(-)CD56(-) tumor-infiltrated lymphocytes appear to be independent prognostic factors of short progression-free survival. High NKG2D expression on CD8(+)tumor-infiltrated lymphocytes, low level of regulatory T-cell tumor-infiltrated lymphocytes, and low PD-L1 expression on circulating T cells were retained in the multivariate Cox analysis model to predict prolonged overall survival. Prospective studies are needed to determine whether such immunological markers may guide adjuvant therapies in stage III metastatic melanomas.Entities:
Mesh:
Year: 2016 PMID: 26829031 PMCID: PMC6156792 DOI: 10.1016/j.jid.2015.12.042
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551