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. 2021 May 22;2021:9912188. doi: 10.1155/2021/9912188

Table 2.

Clinical studies on the application of TLR agonists for cancer treatment published since 2016.

Target TLR TLR agonist Companion treatment Conditions Phase Results Reference
TLR2 CADI-05 Chemotherapy (cisplatin-paclitaxel) Non-small-cell lung cancer II No survival benefit was observed with the addition of CADI-05 to chemotherapy. [143]
TLR3 Poly-ICLC NY-ESO-1 peptide vaccine Melanoma I/II Enhanced specific CD8+ T cell response. [138]
Peptide-pulsed DCs Pancreatic cancer I The treatment was safe and induced a measurable tumor-specific T cell population. [142]
TLR3, TLR4 Poly-ICLC, LPS Multipeptide vaccine and incomplete Freund's adjuvant Melanoma I Combinations of poly-ICLC or LPS with peptide vaccine and incomplete Freund's adjuvant are safe and induce T cell response. [99]
TLR4 TLR9 AS15 Recombinant MAGE-A3 vaccine Melanoma I The treatment was tolerated and produced durable Ab responses. [139]
TLR7 Imiquimod Chemotherapy (paclitaxel) Breast cancer cutaneous metastases II The combination was effective in inducing disease regression, but responses were short-lived. [144]
TLR8 Motolimod Anti-EGFR (cetuximab) Head and neck squamous cell carcinoma I The addition of TLR agonist enhanced the cellular antitumor immune response. [140, 141]
TLR9 GNKG168 N/A Minimal residual disease positive acute leukemia I Immunologic changes were observed. [145]