Complete response to PD-1 blockade following EBV-specific T-cell therapy in metastatic nasopharyngeal carcinoma.


Journal

NPJ precision oncology
ISSN: 2397-768X
Titre abrégé: NPJ Precis Oncol
Pays: England
ID NLM: 101708166

Informations de publication

Date de publication:
19 Mar 2021
Historique:
received: 16 08 2020
accepted: 18 02 2021
entrez: 20 3 2021
pubmed: 21 3 2021
medline: 21 3 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 33742086
doi: 10.1038/s41698-021-00162-7
pii: 10.1038/s41698-021-00162-7
pmc: PMC7979738
doi:

Types de publication

Journal Article

Langues

eng

Pagination

24

Subventions

Organisme : Department of Health | National Health and Medical Research Council (NHMRC)
ID : 1132519

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Auteurs

Corey Smith (C)

QIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

Margaret McGrath (M)

Princess Alexandra Hospital, Faculty of Medicine, University of Queensland, Brisbane, Australia.

Michelle A Neller (MA)

QIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

Katherine K Matthews (KK)

QIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

Pauline Crooks (P)

QIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

Laetitia Le Texier (L)

QIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

Benedict Panizza (B)

Princess Alexandra Hospital, Faculty of Medicine, University of Queensland, Brisbane, Australia.

Sandro Porceddu (S)

Princess Alexandra Hospital, Faculty of Medicine, University of Queensland, Brisbane, Australia.

Rajiv Khanna (R)

QIMR Berghofer Centre for Immunotherapy and Vaccine Development and Tumour Immunology Laboratory, Department of Immunology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia. rajiv.khanna@qimr.edu.au.

Classifications MeSH