TY - JOUR
T1 - Trial Watch
T2 - Toll-like receptor agonists in oncological indications
AU - Aranda, Fernando
AU - Vacchelli, Erika
AU - Obrist, Florine
AU - Eggermont, Alexander
AU - Galon, Jérôme
AU - Sautès-Fridman, Catherine
AU - Cremer, Isabelle
AU - ter Meulen, Jan Henrik
AU - Zitvogel, Laurence
AU - Kroemer, Guido
AU - Galluzzi, Lorenzo
N1 - Funding Information:
Authors are supported by the Ligue contre le Cancer (équipe labelisée); Agence National de la Recherche (ANR); Association pour la recherche sur le cancer (ARC); Cancéropôle Ile-de-France; AXA Chair for Longevity Research; Institut National du Cancer (INCa); Fondation Bettencourt-Schueller; Fondation de France; Fondation pour la Recherche Médicale (FRM); the European Commission (ArtForce); the European Research Council (ERC); the LabEx Immuno-Oncology; the SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE); the SIRIC Cancer Research and Personalized Medicine (CARPEM); and the Paris Alliance of Cancer Research Institutes (PACRI).
PY - 2014/1/1
Y1 - 2014/1/1
N2 - Toll-like receptors (TLRs) are an evolutionarily conserved group of enzymatically inactive, single membranespanning proteins that recognize a wide panel of exogenous and endogenous danger signals. Besides constituting a crucial component of the innate immune response to bacterial and viral pathogens, TLRs appear to play a major role in anticancer immunosurveillance. In line with this notion, several natural and synthetic TLR ligands have been intensively investigated for their ability to boost tumor-targeting immune responses elicited by a variety of immunotherapeutic and chemotherapeutic interventions. Three of these agents are currently approved by the US Food and Drug Administration (FDA) or equivalent regulatory agencies for use in cancer patients: the so-called bacillus Calmette-Guérin, monophosphoryl lipid A, and imiquimod. However, the number of clinical trials testing the therapeutic potential of both FDA-approved and experimental TLR agonists in cancer patients is stably decreasing, suggesting that drug developers and oncologists are refocusing their interest on alternative immunostimulatory agents. Here, we summarize recent findings on the use of TLR agonists in cancer patients and discuss how the clinical evaluation of FDA-approved and experimental TLR ligands has evolved since the publication of our first Trial Watch dealing with this topic.
AB - Toll-like receptors (TLRs) are an evolutionarily conserved group of enzymatically inactive, single membranespanning proteins that recognize a wide panel of exogenous and endogenous danger signals. Besides constituting a crucial component of the innate immune response to bacterial and viral pathogens, TLRs appear to play a major role in anticancer immunosurveillance. In line with this notion, several natural and synthetic TLR ligands have been intensively investigated for their ability to boost tumor-targeting immune responses elicited by a variety of immunotherapeutic and chemotherapeutic interventions. Three of these agents are currently approved by the US Food and Drug Administration (FDA) or equivalent regulatory agencies for use in cancer patients: the so-called bacillus Calmette-Guérin, monophosphoryl lipid A, and imiquimod. However, the number of clinical trials testing the therapeutic potential of both FDA-approved and experimental TLR agonists in cancer patients is stably decreasing, suggesting that drug developers and oncologists are refocusing their interest on alternative immunostimulatory agents. Here, we summarize recent findings on the use of TLR agonists in cancer patients and discuss how the clinical evaluation of FDA-approved and experimental TLR ligands has evolved since the publication of our first Trial Watch dealing with this topic.
KW - BCG
KW - CpG-7909
KW - Damage-associated molecular patterns
KW - Hiltonol™
KW - Polyi:C
KW - Resiquimod
UR - http://www.scopus.com/inward/record.url?scp=84906871563&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:84906871563
SN - 2162-4011
VL - 3
JO - OncoImmunology
JF - OncoImmunology
IS - 7
M1 - e29179
ER -