TY - JOUR
T1 - Trial Watch
T2 - Immunotherapy plus radiation therapy for oncological indications
AU - Vacchelli, Erika
AU - Bloy, Norma
AU - Aranda, Fernando
AU - Buqué, Aitziber
AU - Cremer, Isabelle
AU - Demaria, Sandra
AU - Eggermont, Alexander
AU - Formenti, Silvia Chiara
AU - Fridman, Wolf Hervé
AU - Fucikova, Jitka
AU - Galon, Jérôme
AU - Spisek, Radek
AU - Tartour, Eric
AU - Zitvogel, Laurence
AU - Kroemer, Guido
AU - Galluzzi, Lorenzo
N1 - Publisher Copyright:
© 2016 Taylor & Francis Group, LLC.
PY - 2016/9/1
Y1 - 2016/9/1
N2 - Malignant cells succumbing to some forms of radiation therapy are particularly immunogenic and hence can initiate a therapeutically relevant adaptive immune response. This reflects the intrinsic antigenicity of malignant cells (which often synthesize a high number of potentially reactive neo-antigens) coupled with the ability of radiation therapy to boost the adjuvanticity of cell death as it stimulates the release of endogenous adjuvants from dying cells. Thus, radiation therapy has been intensively investigated for its capacity to improve the therapeutic profile of several anticancer immunotherapies, including (but not limited to) checkpoint blockers, anticancer vaccines, oncolytic viruses, Toll-like receptor (TLR) agonists, cytokines, and several small molecules with immunostimulatory effects. Here, we summarize recent preclinical and clinical advances in this field of investigation.
AB - Malignant cells succumbing to some forms of radiation therapy are particularly immunogenic and hence can initiate a therapeutically relevant adaptive immune response. This reflects the intrinsic antigenicity of malignant cells (which often synthesize a high number of potentially reactive neo-antigens) coupled with the ability of radiation therapy to boost the adjuvanticity of cell death as it stimulates the release of endogenous adjuvants from dying cells. Thus, radiation therapy has been intensively investigated for its capacity to improve the therapeutic profile of several anticancer immunotherapies, including (but not limited to) checkpoint blockers, anticancer vaccines, oncolytic viruses, Toll-like receptor (TLR) agonists, cytokines, and several small molecules with immunostimulatory effects. Here, we summarize recent preclinical and clinical advances in this field of investigation.
KW - Danger-associated molecular patterns
KW - TGFβ1
KW - immunogenic cell death
KW - ipilimumab
KW - nivolumab
KW - pembrolizumab
UR - http://www.scopus.com/inward/record.url?scp=84986253403&partnerID=8YFLogxK
U2 - 10.1080/2162402X.2016.1214790
DO - 10.1080/2162402X.2016.1214790
M3 - Review article
AN - SCOPUS:84986253403
SN - 2162-4011
VL - 5
JO - OncoImmunology
JF - OncoImmunology
IS - 9
M1 - e1214790
ER -