Immunotherapy and the concept of a clinical cure

被引:39
作者
Eggermont, Alexander M. M. [1 ,2 ]
Kroemer, Guido [1 ,3 ,4 ,5 ,6 ]
Zitvogel, Laurence [2 ,7 ,8 ]
机构
[1] Inst Gustave Roussy, F-94805 Villejuif, France
[2] Univ Paris 11, F-94270 Le Kremlin Bicetre, France
[3] INSERM, U848, F-94805 Villejuif, France
[4] Univ Paris 05, Sorbonne Paris Cite, F-75006 Paris, France
[5] Ctr Rech Cordeliers, Equipe Labellise Ligue Canc 11, F-75006 Paris, France
[6] Hop Europeen Georges Pompidou, AP HP, F-75015 Paris, France
[7] INSERM, U1015, F-94805 Villejuif, France
[8] Inst Gustave Roussy, Ctr Clin Invest, CBT507, F-94805 Villejuif, France
关键词
Immunotherapy; Anti-PD-1; Ipilimumab; Immunogenic cell death; Clinical cure; METASTATIC MELANOMA; IMPROVED SURVIVAL; MEK INHIBITION; IMMUNE-SYSTEM; BRAF; VEMURAFENIB; IMPROVES;
D O I
10.1016/j.ejca.2013.06.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Immunotherapy has entered a new phase in its history, i.e. the phase of being broadly accepted as a key component of therapeutic strategies to control and cure cancer. Immune-modulation by checkpoint inhibitors have demonstrated to be capable of inducing long lasting tumour responses. Breaking tolerance by ipilimumab has been a crucial event in the past recent years, but PD-1/PD-L1 antibodies have forever changed the landscape in oncology in 2013. The most mature results have been obtained in advanced melanoma patients. High response rates of high quality with prolonged duration have been demonstrated in melanoma, renal cancer and in lung cancer. The broad potential is now being explored across a wide range of tumours. Importantly, synergy with ipilimumab has been demonstrated in melanoma, indicating a bright further future. Long term tumour control now seems achievable and thus the concept of a "clinical cure" is emerging. These antibodies bring immunotherapy to the forefront and indicate that immune-modulation will be a key component of therapeutic strategies from now on. All these observations indicate that "clinical cures" can only be achieved when the immune system is involved, and so the true renaissance of immunotherapy has arrived. (C) 2013 Published by Elsevier Ltd.
引用
收藏
页码:2965 / 2967
页数:3
相关论文
共 23 条
[1]
[Anonymous], N ENGL J MED
[2]
[Anonymous], J CLIN ONCOL S
[3]
Toll-like receptor 4-dependent contribution of the immune system to anticancer chemotherapy and radiotherapy [J].
Apetoh, Lionel ;
Ghiringhelli, Francois ;
Tesniere, Antoine ;
Obeid, Michel ;
Ortiz, Carla ;
Criollo, Alfredo ;
Mignot, Gregoire ;
Maiuri, M. Chiara ;
Ullrich, Evelyn ;
Saulnier, Patrick ;
Yang, Huan ;
Amigorena, Sebastian ;
Ryffel, Bernard ;
Barrat, Franck J. ;
Saftig, Paul ;
Levi, Francis ;
Lidereau, Rosette ;
Nogues, Catherine ;
Mira, Jean-Paul ;
Chompret, Agnes ;
Joulin, Virginie ;
Clavel-Chapelon, Francoise ;
Bourhis, Jean ;
Andre, Fabrice ;
Delaloge, Suzette ;
Tursz, Thomas ;
Kroemer, Guido ;
Zitvogel, Laurence .
NATURE MEDICINE, 2007, 13 (09) :1050-1059
[4]
Autoimmunity correlates with tumor regression in patients with metastatic melanoma treated with anti-cytotoxic T-lymphocyte antigen-4 [J].
Attia, P ;
Phan, GQ ;
Maker, AV ;
Robinson, MR ;
Quezado, MM ;
Yang, JC ;
Sherry, RM ;
Topalian, SL ;
Kammula, US ;
Royal, RE ;
Restifo, NP ;
Haworth, LR ;
Levy, C ;
Mavroukakis, SA ;
Nichol, G ;
Yellin, MJ ;
Rosenberg, SA .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) :6043-6053
[5]
Brahmer JR, 2013, J CLIN ONCOL, V31
[6]
Improved Survival with Vemurafenib in Melanoma with BRAF V600E Mutation [J].
Chapman, Paul B. ;
Hauschild, Axel ;
Robert, Caroline ;
Haanen, John B. ;
Ascierto, Paolo ;
Larkin, James ;
Dummer, Reinhard ;
Garbe, Claus ;
Testori, Alessandro ;
Maio, Michele ;
Hogg, David ;
Lorigan, Paul ;
Lebbe, Celeste ;
Jouary, Thomas ;
Schadendorf, Dirk ;
Ribas, Antoni ;
O'Day, Steven J. ;
Sosman, Jeffrey A. ;
Kirkwood, John M. ;
Eggermont, Alexander M. M. ;
Dreno, Brigitte ;
Nolop, Keith ;
Li, Jiang ;
Nelson, Betty ;
Hou, Jeannie ;
Lee, Richard J. ;
Flaherty, Keith T. ;
McArthur, Grant A. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 364 (26) :2507-2516
[7]
Alternatively spliced NKp30 isoforms affect the prognosis of gastrointestinal stromal tumors [J].
Delahaye, Nicolas F. ;
Rusakiewicz, Sylvie ;
Martins, Isabelle ;
Menard, Cedric ;
Roux, Stephan ;
Lyonnet, Luc ;
Paul, Pascale ;
Sarabi, Matthieu ;
Chaput, Nathalie ;
Semeraro, Michaela ;
Minard-Colin, Veronique ;
Poirier-Colame, Vichnou ;
Chaba, Kariman ;
Flament, Caroline ;
Baud, Veronique ;
Authier, Helene ;
Kerdine-Roemer, Saadia ;
Pallardy, Marc ;
Cremer, Isabelle ;
Peaudecerf, Laetitia ;
Rocha, Benedita ;
Valteau-Couanet, Dominique ;
Gutierrez, Javier Celis ;
Nunes, Jacques A. ;
Commo, Frederic ;
Bonvalot, Sylvie ;
Ibrahim, Nicolas ;
Terrier, Philippe ;
Opolon, Paule ;
Bottino, Cristina ;
Moretta, Alessandro ;
Tavernier, Jan ;
Rihet, Pascal ;
Coindre, Jean-Michel ;
Blay, Jean-Yves ;
Isambert, Nicolas ;
Emile, Jean-Francois ;
Vivier, Eric ;
Lecesne, Axel ;
Kroemer, Guido ;
Zitvogel, Laurence .
NATURE MEDICINE, 2011, 17 (06) :700-+
[8]
BRAF inhibition improves tumor recognition by the immune system Potential implications for combinatorial therapies against melanoma involving adoptive T-cell transfer [J].
Donia, Marco ;
Fagone, Paolo ;
Nicoletti, Ferdinando ;
Andersen, Rikke Sick ;
Hogdall, Estrid ;
Straten, Per Thor ;
Andersen, Mads Hald ;
Svane, Inge Marie .
ONCOIMMUNOLOGY, 2012, 1 (09) :1476-1483
[9]
Improved Survival with MEK Inhibition in BRAF-Mutated Melanoma [J].
Flaherty, Keith T. ;
Robert, Caroline ;
Hersey, Peter ;
Nathan, Paul ;
Garbe, Claus ;
Milhem, Mohammed ;
Demidov, Lev V. ;
Hassel, Jessica C. ;
Rutkowski, Piotr ;
Mohr, Peter ;
Dummer, Reinhard ;
Trefzer, Uwe ;
Larkin, James M. G. ;
Utikal, Jochen ;
Dreno, Brigitte ;
Nyakas, Marta ;
Middleton, Mark R. ;
Becker, Juergen C. ;
Casey, Michelle ;
Sherman, Laurie J. ;
Wu, Frank S. ;
Ouellet, Daniele ;
Martin, Anne-Marie ;
Patel, Kiran ;
Schadendorf, Dirk .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 367 (02) :107-114
[10]
Immunogenic and tolerogenic cell death [J].
Green, Douglas R. ;
Ferguson, Thomas ;
Zitvogel, Laurence ;
Kroemer, Guido .
NATURE REVIEWS IMMUNOLOGY, 2009, 9 (05) :353-363