| Literature DB >> 33742086 |
Corey Smith1, Margaret McGrath2, Michelle A Neller1, Katherine K Matthews1, Pauline Crooks1, Laetitia Le Texier1, Benedict Panizza2, Sandro Porceddu2, Rajiv Khanna3.
Abstract
Nasopharyngeal carcinoma (NPC) is an Epstein-Barr virus (EBV)-associated heterogeneous disease and is characterized by peritumoral immune infiltrate. Adoptive T-cell therapy (ACT) has emerged as a potential therapeutic strategy for NPC. However, the tumor microenvironment remains a major roadblock for the successful implementation of ACT in clinical settings. Expression of checkpoint molecules by malignant cells can inhibit the effector function of adoptively transferred EBV-specific T cells. Here we present a novel case report of a patient with metastatic NPC who was successfully treated with a combination of EBV-specific ACT and programmed cell death-1 blockade therapy. Following combination immunotherapy, the patient showed complete resolution of metastatic disease with no evidence of disease relapse for 22 months. Follow-up immunological analysis revealed dramatic restructuring of the global T-cell repertoire that was coincident with the clinical response. This case report provides an important platform for translating these findings to a larger cohort of NPC patients.Entities:
Year: 2021 PMID: 33742086 PMCID: PMC7979738 DOI: 10.1038/s41698-021-00162-7
Source DB: PubMed Journal: NPJ Precis Oncol ISSN: 2397-768X