Frontiers in Immunology (Jan 2025)

Pilot clinical trial of neoadjuvant toll-like receptor 7 agonist (Imiquimod) immunotherapy in early-stage oral squamous cell carcinoma

  • Angela J. Yoon,
  • Richard D. Carvajal,
  • Evan M. Graboyes,
  • John M. Kaczmar,
  • William G. Albergotti,
  • Alexandra E. Kejner,
  • Scott H. Troob,
  • Elizabeth Philipone,
  • Jean-Sebastien Anoma,
  • Kent E. Armeson,
  • Elizabeth G. Hill,
  • Mary S. Richardson,
  • Tina R. Woods,
  • Bhishamjit S. Chera,
  • Farzad Nourollah-Zadeh,
  • Byung J. Lee,
  • Subramanya Pandruvada,
  • Antonis Kourtidis,
  • Christina Kingsley,
  • Elizabeth C. O’Quinn,
  • Stephanie Mills,
  • Victoria C. Jordan,
  • Mike Spencer,
  • Danielle Fails,
  • Trevor D. McKee,
  • Mark Zaidi,
  • Alan Brisendine,
  • Shane Horn,
  • Shikhar Mehrotra,
  • Besim Ogretmen,
  • Jason G. Newman

DOI
https://doi.org/10.3389/fimmu.2025.1530262
Journal volume & issue
Vol. 16

Abstract

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BackgroundThere is no neoadjuvant immunotherapy for early-stage oral cancer patients. We report a single-arm, open-label, pilot clinical trial assessing the efficacy and safety of topical toll-like receptor-7 (TLR-7) agonist, imiquimod, utilized in a neoadjuvant setting in early-stage oral squamous cell carcinoma (OSCC).MethodsThe primary endpoint is reduction in tumor cell counts assessed by quantitative multiplex immunofluorescence and the immune-related pathologic response. The secondary endpoint is safety.Results60% of patients experienced a 50% reduction or greater in tumor cell count post-treatment (95% CI = 32% to 84%). Similarly, 60% of patients had immune-related major pathologic response (irMPR) with two complete pathologic responses, and 40% had partial response (PR) with the percent residual viable tumor ranging from 25% to 65%. An increase in functional helper and cytotoxic T-cells significantly contributed to a reduction in tumor (R=0.54 and 0.55, respectively). The treatment was well tolerated with the application site mucositis being the most common adverse event (grades 1-3), and no grade 4 life-threatening event. The median follow-up time was 17 months (95% CI = 16 months - not reached), and one-year recurrence-free survival was 93% of evaluable patients.ConclusionNeoadjuvant imiquimod immunotherapy could be safe and promising regimen for early-stage oral cancer.Trial registrationClinicalTrials.gov, Identifier NCT04883645.

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