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Use of nonsteroidal anti-inflammatory drugs predicts improved patient survival for PIK3CA-altered head and neck cancer.

Matthew L HedbergNoah D PeyserJulie E BaumanWilliam E GoodingHua LiNeil E BholaTian Ran ZhuYan ZengToni M BrandMi-Ok KimRichard C K JordanScott VandenBergVictor OlivasTrever G BivonaSimion I ChioseaLin WangGordon B MillsJonas T JohnsonUmamaheswar DuvvuriRobert L FerrisPatrick HaDaniel E JohnsonJennifer R Grandis
Published in: The Journal of experimental medicine (2019)
PIK3CA is the most commonly altered oncogene in head and neck squamous cell carcinoma (HNSCC). We evaluated the impact of nonsteroidal anti-inflammatory drugs (NSAIDs) on survival in a PIK3CA-characterized cohort of 266 HNSCC patients and explored the mechanism in relevant preclinical models including patient-derived xenografts. Among subjects with PIK3CA mutations or amplification, regular NSAID use (≥6 mo) conferred markedly prolonged disease-specific survival (DSS; hazard ratio 0.23, P = 0.0032, 95% CI 0.09-0.62) and overall survival (OS; hazard ratio 0.31, P = 0.0043, 95% CI 0.14-0.69) compared with nonregular NSAID users. For PIK3CA-altered HNSCC, predicted 5-yr DSS was 72% for NSAID users and 25% for nonusers; predicted 5-yr OS was 78% for regular NSAID users and 45% for nonregular users. PIK3CA mutation predicted sensitivity to NSAIDs in preclinical models in association with increased systemic PGE2 production. These findings uncover a biologically plausible rationale to implement NSAID therapy in PIK3CA-altered HNSCC.
Keyphrases
  • anti inflammatory drugs
  • protein kinase
  • free survival
  • clinical trial
  • newly diagnosed
  • stem cells
  • cell therapy
  • chronic kidney disease
  • patient reported outcomes
  • bone marrow
  • nucleic acid