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

被引:3
作者
Yoon, Angela J. [1 ]
Carvajal, Richard D. [2 ]
Graboyes, Evan M. [1 ]
Kaczmar, John M. [1 ]
Albergotti, William G. [1 ]
Kejner, Alexandra E. [1 ]
Troob, Scott H. [3 ]
Philipone, Elizabeth [3 ]
Anoma, Jean-Sebastien [1 ]
Armeson, Kent E. [1 ]
Hill, Elizabeth G. [1 ]
Richardson, Mary S. [1 ]
Woods, Tina R. [1 ]
Chera, Bhishamjit S. [1 ]
Nourollah-Zadeh, Farzad [1 ]
Lee, Byung J. [1 ]
Pandruvada, Subramanya [1 ]
Kourtidis, Antonis [1 ]
Kingsley, Christina [1 ]
O'Quinn, Elizabeth C. [1 ]
Mills, Stephanie [1 ]
Jordan, Victoria C. [1 ]
Spencer, Mike [4 ]
Fails, Danielle [4 ]
Mckee, Trevor D. [5 ]
Zaidi, Mark [5 ]
Brisendine, Alan [1 ]
Horn, Shane [1 ]
Mehrotra, Shikhar [1 ]
Ogretmen, Besim [1 ]
Newman, Jason G. [1 ]
机构
[1] Med Univ South Carolina, Charleston, SC 29425 USA
[2] Northwell Hlth Canc Inst, New Hyde Pk, NY USA
[3] Columbia Univ, Irving Med Ctr, New York, NY USA
[4] Fortis Life Sci, Montgomery, TX USA
[5] Pathomics, Toronto, ON, Canada
关键词
oral cancer; neoadjuvant clinical trial; toll-like 7 receptor agonist; imiquimod; immunotherapy; 5-PERCENT CREAM; PHARMACOKINETICS; HEAD;
D O I
10.3389/fimmu.2025.1530262
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background There 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).Methods The primary endpoint is reduction in tumor cell counts assessed by quantitative multiplex immunofluorescence and the immune-related pathologic response. The secondary endpoint is safety.Results 60% 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.Conclusion Neoadjuvant imiquimod immunotherapy could be safe and promising regimen for early-stage oral cancer.Trial registration ClinicalTrials.gov, Identifier NCT04883645.
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页数:12
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