Circulating Plasma Exosomal PD-L1 Predicts Prognosis of Head and Neck Squamous Cell Carcinoma After Radiation Therapy
- Keisuke Tamari 1, Kazumasa Minami 2, Shotaro Tatekawa 1, Yuji Seo 3, Takahito Fukusumi 4, Hidenori Tanaka 4, Motoyuki Suzuki 4, Hirotaka Eguchi 4, Yukinori Takenaka 4, Takero Hirata 1, Kazuhiko Hayashi 1, Fumiaki Isohashi 1, Shinichi Shimizu 3, Masahiko Koizumi 2, Hidenori Inohara 4, Kazuhiko Ogawa 1
- 1Department of Radiation Oncology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
- 2Department of Medical Physics and Engineering, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
- 3Department of Carbon Ion Radiotherapy, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
- 4Department of Otorhinolaryngology-Head and Neck Surgery, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
- 0Department of Radiation Oncology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
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View abstract on PubMed
Summary
This summary is machine-generated.Pretreatment exosomal programmed death-ligand 1 (PD-L1) in plasma predicts outcomes for head and neck squamous cell carcinoma (HNSCC) patients undergoing radiation therapy. High exosomal PD-L1 levels correlate with poorer progression-free survival and local control.
Area Of Science
- Oncology
- Immunotherapy
- Biomarker Discovery
Background
- Radiation therapy is a standard treatment for head and neck squamous cell carcinoma (HNSCC).
- Predictive biomarkers are crucial for optimizing HNSCC treatment strategies.
- Programmed death-ligand 1 (PD-L1) is an immune checkpoint protein implicated in cancer progression.
Purpose Of The Study
- To investigate the association between circulating plasma programmed death-ligand 1 (PD-L1) levels and treatment outcomes in HNSCC patients receiving radiation therapy.
- To determine if pretreatment PD-L1, both total and exosomal, can serve as a prognostic biomarker for HNSCC patients.
Main Methods
- Retrospective analysis of plasma samples from 76 HNSCC patients before radiation therapy.
- Quantification of total and exosomal PD-L1 using enzyme-linked immunosorbent assay.
- Statistical analysis including univariate and multivariate models to assess the correlation between PD-L1 levels and overall survival (OS), progression-free survival (PFS), and local control (LC).
Main Results
- Median total PD-L1 was 115.1 pg/mL; median exosomal PD-L1 was 2.8 pg/mL.
- Elevated pretreatment exosomal PD-L1 was significantly associated with poorer PFS and LC.
- 1-year PFS was 79.2% for high exosomal PD-L1 vs. 33.3% for low (P < .001).
- 1-year LC was 87.3% for high exosomal PD-L1 vs. 50.0% for low (P < .001).
- Total PD-L1 and exosomal PD-L1 did not significantly impact OS.
Conclusions
- Pretreatment circulating exosomal PD-L1 in plasma is a significant prognostic factor for HNSCC patients undergoing radiation therapy.
- Exosomal PD-L1 levels can help predict progression-free survival and local control.
- This finding supports the potential utility of exosomal PD-L1 as a predictive biomarker in HNSCC management.
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