TY - JOUR
T1 - Trial watch
T2 - Chemotherapy with immunogenic cell death inducers
AU - Vacchelli, Erika
AU - Galluzzi, Lorenzo
AU - Fridman, Wolf Hervé
AU - Galon, Jerome
AU - Sautès-Fridman, Catherine
AU - Tartour, Eric
AU - Zitvogel, Laurence
AU - Kroemer, Guido
N1 - Funding Information:
Authors are supported by the Ligue contre le Cancer (équipes labelisées), AXA Chair for Longevity Research, Cancéropôle Ile-de-France, Institut National du Cancer (INCa), Fondation Bettencourt-Schueller, Fondation de France, Fondation pour la Recherche Médicale, Agence National de la Recherche, the European Commission (Apo-Sys, ArtForce, ChemoRes. Death-Train) and the LabEx Immuno-Oncology.
PY - 2012/10/29
Y1 - 2012/10/29
N2 - The long-established notion that apoptosis would be immunologically silent, and hence it would go unnoticed by the immune system, if not tolerogenic, and hence it would actively suppress immune responses, has recently been revisited. In some instances, indeed, cancer cells undergo apoptosis while emitting a spatiotemporally-defined combination of signals that renders them capable of eliciting a long-term protective antitumor immune response. Importantly, only a few anticancer agents can stimulate such an immunogenic cell death. These include cyclophosphamide, doxorubicin and oxaliplatin, which are currently approved by FDA for the treatment of multiple hematologic and solid malignancies, as well as mitoxantrone, which is being used in cancer therapy and against multiple sclerosis. In this Trial Watch, we will review and discuss the progress of recent (initiated after January 2008) clinical trials evaluating the off-label use of cyclophosphamide, doxorubicin, oxaliplatin and mitoxantrone.
AB - The long-established notion that apoptosis would be immunologically silent, and hence it would go unnoticed by the immune system, if not tolerogenic, and hence it would actively suppress immune responses, has recently been revisited. In some instances, indeed, cancer cells undergo apoptosis while emitting a spatiotemporally-defined combination of signals that renders them capable of eliciting a long-term protective antitumor immune response. Importantly, only a few anticancer agents can stimulate such an immunogenic cell death. These include cyclophosphamide, doxorubicin and oxaliplatin, which are currently approved by FDA for the treatment of multiple hematologic and solid malignancies, as well as mitoxantrone, which is being used in cancer therapy and against multiple sclerosis. In this Trial Watch, we will review and discuss the progress of recent (initiated after January 2008) clinical trials evaluating the off-label use of cyclophosphamide, doxorubicin, oxaliplatin and mitoxantrone.
KW - ATP
KW - Autophagy
KW - Calreticulin
KW - HMGB1
KW - HSP70
KW - Interferon γ
UR - http://www.scopus.com/inward/record.url?scp=84878019374&partnerID=8YFLogxK
U2 - 10.4161/onci.1.2.19026
DO - 10.4161/onci.1.2.19026
M3 - Review article
AN - SCOPUS:84878019374
SN - 2162-4011
VL - 1
SP - 179
EP - 188
JO - OncoImmunology
JF - OncoImmunology
IS - 2
ER -