Complete response to PD-1 blockade following EBV-specific T-cell therapy in metastatic nasopharyngeal carcinoma.
Corey SmithMargaret McGrathMichelle A NellerKatherine K MatthewsPauline CrooksLaetitia Le TexierBenedict PanizzaSandro PorcedduRajiv KhannaPublished in: NPJ precision oncology (2021)
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.
Keyphrases
- epstein barr virus
- case report
- cell therapy
- diffuse large b cell lymphoma
- squamous cell carcinoma
- small cell lung cancer
- end stage renal disease
- healthcare
- newly diagnosed
- induced apoptosis
- primary care
- stem cells
- ejection fraction
- poor prognosis
- peritoneal dialysis
- cell cycle
- oxidative stress
- regulatory t cells
- single cell
- signaling pathway
- cell proliferation
- endoplasmic reticulum stress
- data analysis