@article{9a5f9b4f7250430fa501be01c83b6f4d,
title = "Trial watch: chemotherapy-induced immunogenic cell death in immuno-oncology",
abstract = "The term 'immunogenic cell death' (ICD) denotes an immunologically unique type of regulated cell death that enables, rather than suppresses, T cell-driven immune responses that are specific for antigens derived from the dying cells. The ability of ICD to elicit adaptive immunity heavily relies on the immunogenicity of dying cells, implying that such cells must encode and present antigens not covered by central tolerance (antigenicity), and deliver immunostimulatory molecules such as damage-associated molecular patterns and cytokines (adjuvanticity). Moreover, the host immune system must be equipped to detect the antigenicity and adjuvanticity of dying cells. As cancer (but not normal) cells express several antigens not covered by central tolerance, they can be driven into ICD by some therapeutic agents, including (but not limited to) chemotherapeutics of the anthracycline family, oxaliplatin and bortezomib, as well as radiation therapy. In this Trial Watch, we describe current trends in the preclinical and clinical development of ICD-eliciting chemotherapy as partner for immunotherapy, with a focus on trials assessing efficacy in the context of immunomonitoring.",
keywords = "Antigen-presenting cell, autophagy, cytotoxic T lymphocyte, endoplasmic reticulum stress, CAR T cells, cytokines, chemokines, dendritic cell, immune checkpoint blocker, type I interferon, CD8(+) T-CELLS, RANDOMIZED PHASE-2 TRIAL, BREAST-CANCER PATIENTS, SOFT-TISSUE SARCOMA, FIND-ME SIGNAL, DENDRITIC CELLS, CHECKPOINT BLOCKADE, APOPTOTIC CELLS, CALRETICULIN EXPOSURE, ANTITUMOR IMMUNITY",
author = "Isaure Vanmeerbeek and Jenny Sprooten and {De Ruysscher}, Dirk and Sabine Tejpar and Peter Vandenberghe and Jitka Fucikova and Radek Spisek and Laurence Zitvogel and Guido Kroemer and Lorenzo Galluzzi and Garg, {Abhishek D.}",
note = "Funding Information: ADG is supported by Research Foundation Flanders{\textquoteright} (FWO) Excellence of Science (EOS) grant (30837538) for the {\textquoteleft}DECODE{\textquoteright} consortium and the KU Leuven via the C1 grant (C14/19/098) as well as the POR award funds (POR/16/040). ST is supported by Research Foundation Flanders{\textquoteright} (FWO) as a Senior Clinical Investigator and by the Stichting tegen Kanker. GK is supported by the Ligue contre le Cancer ({\'E}quipe Labellis{\'e}e); Agence National de la Recherche (ANR) – Projets blancs; ANR under the frame of E-Rare-2, the ERA-Net for Research on Rare Diseases; Association pour la recherche sur le cancer (ARC); Canc{\'e}rop{\^o}le Ile-de-France; Chancelerie des universit{\'e}s de Paris (Legs Poix), Fondation pour la Recherche M{\'e}dicale (FRM); a donation by Elior; European Research Area Network on Cardiovascular Diseases (ERA-CVD, MINOTAUR); Gustave Roussy Odyssea, the European Union Horizon 2020 Project Oncobiome; Fondation Carrefour; High-end Foreign Expert Program in China (GDW20171100085 and GDW20181100051), Institut National du Cancer (INCa); Inserm (HTE); Institut Universitaire de France; LeDucq Foundation; the LabEx Immuno-Oncology; the RHU Torino Lumi{\`e}re; the Seerave Foundation; the SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE); and the SIRIC Cancer Research and Personalized Medicine (CARPEM). The LG lab is supported by a Breakthrough Level 2 grant from the US Department of Defense (DoD), Breast Cancer Research Program (BCRP) (#BC180476P1), by a startup grant from the Dept. of Radiation Oncology at Weill Cornell Medicine (New York, US), by industrial collaborations with Lytix (Oslo, Norway) and Phosplatin (New York, US), and by donations from Phosplatin (New York, US), the Luke Heller TECPR2 Foundation (Boston, US) and Sotio a.s. (Prague, Czech Republic). Funding Information: ADG is supported by Research Foundation Flanders? (FWO) Excellence of Science (EOS) grant (30837538) for the ?DECODE? consortium and the KU Leuven via the C1 grant (C14/19/098) as well as the POR award funds (POR/16/040). ST is supported by Research Foundation Flanders? (FWO) as a Senior Clinical Investigator and by the Stichting tegen Kanker. GK is supported by the Ligue contre le Cancer (?quipe Labellis?e); Agence National de la Recherche (ANR)?Projets blancs; ANR under the frame of E-Rare-2, the ERA-Net for Research on Rare Diseases; Association pour la recherche sur le cancer (ARC); Canc?rop?le Ile-de-France; Chancelerie des universit?s de Paris (Legs Poix), Fondation pour la Recherche M?dicale (FRM); a donation by Elior; European Research Area Network on Cardiovascular Diseases (ERA-CVD, MINOTAUR); Gustave Roussy Odyssea, the European Union Horizon 2020 Project Oncobiome; Fondation Carrefour; High-end Foreign Expert Program in China (GDW20171100085 and GDW20181100051), Institut National du Cancer (INCa); Inserm (HTE); Institut Universitaire de France; LeDucq Foundation; the LabEx Immuno-Oncology; the RHU Torino Lumi?re; the Seerave Foundation; the SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE); and the SIRIC Cancer Research and Personalized Medicine (CARPEM). The LG lab is supported by a Breakthrough Level 2 grant from the US Department of Defense (DoD), Breast Cancer Research Program (BCRP) (#BC180476P1), by a startup grant from the Dept. of Radiation Oncology at Weill Cornell Medicine (New York, US), by industrial collaborations with Lytix (Oslo, Norway) and Phosplatin (New York, US), and by donations from Phosplatin (New York, US), the Luke Heller TECPR2 Foundation (Boston, US) and Sotio a.s. (Prague, Czech Republic). Publisher Copyright: {\textcopyright} 2020, {\textcopyright} 2020 The Author(s). Published with license by Taylor & Francis Group, LLC.",
year = "2020",
doi = "10.1080/2162402X.2019.1703449",
language = "English",
volume = "9",
journal = "OncoImmunology ",
issn = "2162-402X",
publisher = "Landes Bioscience",
number = "1",
}