Er:YAG laser-PDT combined with anti- programmed cell death protein-1 for refractory oral potential malignant disorders following oral squamous cell carcinoma surgery
Year: 2026
Type: article
Study design: Case Report
Abstract: • The combination of Er:YAG-PDT and anti-PD-1 immunotherapy achieved complete clearance of local refractory OPMDs. • Elevated NK cell levels, reduced Treg cell percentage, and stable CD8⁺ T cell counts provide preliminary evidence that the combination therapy activates adaptive immunity while maintaining immune homeostasis. • The study identifies Er:YAG-PDT plus anti-PD-1 therapy as a promising treatment option for high-risk OPMDs patients. Oral potential malignant disorders (OPMDs) have a high risk of malignant transformation and recurrence. This case reports describes a novel therapeutic strategy of Er:YAG laser-assisted photodynamic therapy (Er:YAG-PDT) combined with anti-programmed death protein-1 (anti-PD-1) immunotherapy for a patient with refractory OPMDs in the right lower gingiva following oral squamous cell carcinoma (OSCC) surgery on the contralateral side. Initial PDT alone showed limited efficacy, but after integrating Er:YAG laser pretreatment, the patient achieved significant lesion regression, with a complete final clearance. The 6-month follow-up showed good local lesion control in the patient peripheral blood analysis revealed elevated natural killer (NK) cell level and reduced regulatory T (Treg) cell percentage, suggesting activated adaptive immunity, while similar CD8⁺ T cell levels indicated maintained immune homeostasis. This case report highlights the potential of combined Er:YAG-PDT and anti-PD-1 therapy for OPMDs, while emphasizing the need for optimized monitoring and multi-modal strategies to prevent recurrence in high-risk patients.
Authors: Qisheng Rao, Cong Feng, ShiQin Wang, Hongliang Xie, Li Yuan, Guoquan Zhang, Nianhong Qin
Language: English
Subfield: Periodontics
Field: Dentistry
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,610
OpenAlex ID: W7127888065
