| Literature DB >> 33707233 |
Cara Haymaker1, Daniel H Johnson2, Ravi Murthy3, Salah-Eddine Bentebibel2, Marc I Uemura2, Courtney W Hudgens1, Houssein Safa2, Marihella James2, Robert H I Andtbacka4, Douglas B Johnson5, Montaser Shaheen6, Michael A Davies2, Shah Rahimian7, Srinivas K Chunduru7, Denái R Milton8, Michael T Tetzlaff1,9, Willem W Overwijk2, Patrick Hwu2, Nashat Gabrail10, Sudhir Agrawal11, Gary Doolittle12, Igor Puzanov13, Joseph Markowitz14, Chantale Bernatchez15, Adi Diab15.
Abstract
Many patients with advanced melanoma are resistant to immune checkpoint inhibition. In the ILLUMINATE-204 phase I/II trial, we assessed intratumoral tilsotolimod, an investigational Toll-like receptor 9 agonist, with systemic ipilimumab in patients with anti-PD-1- resistant advanced melanoma. In all patients, 48.4% experienced grade 3/4 treatment-emergent adverse events. The overall response rate at the recommended phase II dose of 8 mg was 22.4%, and an additional 49% of patients had stable disease. Responses in noninjected lesions and in patients expected to be resistant to ipilimumab monotherapy were observed. Rapid induction of a local IFNα gene signature, dendritic cell maturation and enhanced markers of antigen presentation, and T-cell clonal expansion correlated with clinical response. A phase III clinical trial with this combination (NCT03445533) is ongoing. SIGNIFICANCE: Despite recent developments in advanced melanoma therapies, most patients do not experience durable responses. Intratumoral tilsotolimod injection elicits a rapid, local type 1 IFN response and, in combination with ipilimumab, activates T cells to promote clinical activity, including in distant lesions and patients not expected to respond to ipilimumab alone.This article is highlighted in the In This Issue feature, p. 1861. ©2021 American Association for Cancer Research.Entities:
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Year: 2021 PMID: 33707233 PMCID: PMC8544022 DOI: 10.1158/2159-8290.CD-20-1546
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397