Immunotherapy for gastric cancers: emerging role and future perspectives

被引:39
作者
Bonotto, Marta [1 ,2 ]
Garattini, Silvio Ken [1 ,2 ]
Basile, Debora [1 ,2 ]
Ongaro, Elena [1 ,2 ]
Fanotto, Valentina [1 ,2 ]
Cattaneo, Monica [1 ,2 ]
Cortiula, Francesco [1 ,2 ]
Iacono, Donatella [1 ]
Cardellino, Giovanni Gerardo [1 ]
Pella, Nicoletta [1 ]
Fasola, Gianpiero [1 ]
Antonuzzo, Lorenzo [3 ]
Silvestris, Nicola [4 ]
Aprile, Giuseppe [1 ,5 ]
机构
[1] Univ Hosp Udine, Dept Oncol, Udine, Italy
[2] Univ Udine, Dept Med Area, Udine, Italy
[3] Univ Hosp Careggi, Med Oncol, Florence, Italy
[4] Natl Canc Inst IRCCS Giovanni Paolo II, Med Oncol Unit, Bari, Italy
[5] ULSS8 Ber, Gen Hosp San Bortolo, Dept Oncol, Vicenza, Italy
关键词
Gastric cancer; immunotherapy; PD-L1; PD-L2; molecular classification; MICROSATELLITE INSTABILITY; PD-L1; EXPRESSION; PHASE-II; MOLECULAR CHARACTERIZATION; IMMUNE MICROENVIRONMENT; ANTI-PD-L1; ANTIBODY; NIVOLUMAB; MELANOMA; COMBINATION; IPILIMUMAB;
D O I
10.1080/17512433.2017.1313113
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: The broad use of immunotherapy is revolutionizing the treatment paradigms of many solid tumors. Although chemotherapy remains the treatment backbone for advanced gastric cancer, improvements in its molecular characterization and progresses in understanding its underpinning biology have supported clinical development of novel immunotherapies. However, the results of recent trials testing these new agents raise the question on how to identify the patients that could greatly benefit. Areas covered: This article summarizes the current understanding on the biology and the mechanisms underlying different clinical features of gastric cancers. Particularly, after a comprehensive literature search, we speculate whether specific molecular subsets of patients could derive more benefit from immunotherapy. Expert commentary: Most cancers may evade the immune response, which is normally regulated by a delicate balance between activating and inhibitory signals. For example, both CTLA-4 and PD-1, once linked to PD-L1/2, may inhibit T-cell signaling. The use of agent to harness the power of the immune system appears to be the ultimate frontier in gastric cancer treatment. While anti-CTLA-4 antibodies are minimally active, there is growing evidence for the efficacy of PD1/-L1 inhibitors. The search of predictive factors for immunotherapy will provide key hints towards the optimal use of these agents.
引用
收藏
页码:609 / 619
页数:11
相关论文
共 88 条
  • [1] Signatures of mutational processes in human cancer
    Alexandrov, Ludmil B.
    Nik-Zainal, Serena
    Wedge, David C.
    Aparicio, Samuel A. J. R.
    Behjati, Sam
    Biankin, Andrew V.
    Bignell, Graham R.
    Bolli, Niccolo
    Borg, Ake
    Borresen-Dale, Anne-Lise
    Boyault, Sandrine
    Burkhardt, Birgit
    Butler, Adam P.
    Caldas, Carlos
    Davies, Helen R.
    Desmedt, Christine
    Eils, Roland
    Eyfjord, Jorunn Erla
    Foekens, John A.
    Greaves, Mel
    Hosoda, Fumie
    Hutter, Barbara
    Ilicic, Tomislav
    Imbeaud, Sandrine
    Imielinsk, Marcin
    Jaeger, Natalie
    Jones, David T. W.
    Jones, David
    Knappskog, Stian
    Kool, Marcel
    Lakhani, Sunil R.
    Lopez-Otin, Carlos
    Martin, Sancha
    Munshi, Nikhil C.
    Nakamura, Hiromi
    Northcott, Paul A.
    Pajic, Marina
    Papaemmanuil, Elli
    Paradiso, Angelo
    Pearson, John V.
    Puente, Xose S.
    Raine, Keiran
    Ramakrishna, Manasa
    Richardson, Andrea L.
    Richter, Julia
    Rosenstiel, Philip
    Schlesner, Matthias
    Schumacher, Ton N.
    Span, Paul N.
    Teague, Jon W.
    [J]. NATURE, 2013, 500 (7463) : 415 - +
  • [2] Immunotherapy for Gastric Cancer: A Focus on Immune Checkpoints
    Alsina, Maria
    Moehler, Markus
    Hierro, Cinta
    Guardeno, Raquel
    Tabernero, Josep
    [J]. TARGETED ONCOLOGY, 2016, 11 (04) : 469 - 477
  • [3] [Anonymous], ANTIANGIOGENIC MOL C
  • [4] Apatinib for gastric cancer: are we moving the antiangiogenic strategy any forward?
    Aprile, Giuseppe
    Bonotto, Marta
    Ongaro, Elena
    Garattini, Silvio Ken
    Fanotto, Valentina
    Basile, Debora
    Cattaneo, Monica
    Casagrande, Mariaelena
    Ferrari, Laura
    Cardellino, Giovanni Gerardo
    Ermacora, Paola
    Pella, Nicoletta
    Giovannoni, Mariella
    Fasola, Gianpiero
    [J]. TRANSLATIONAL CANCER RESEARCH, 2016, 5 : S765 - S771
  • [5] Angiogenic inhibitors in gastric cancers and gastroesophageal junction carcinomas: A critical insight
    Aprile, Giuseppe
    Ongaro, Elena
    Del Re, Marzia
    Lutrino, Stefania Eufemia
    Bonotto, Marta
    Ferrari, Laura
    Rihawi, Karim
    Cardellino, Giovanni Gerardo
    Pella, Nicoletta
    Danesi, Romano
    Fasola, Gianpiero
    [J]. CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2015, 95 (02) : 165 - 178
  • [6] Arzimanoglou II, 1998, CANCER-AM CANCER SOC, V82, P1808, DOI 10.1002/(SICI)1097-0142(19980515)82:10<1808::AID-CNCR2>3.0.CO
  • [7] 2-J
  • [8] Effects of MAPK and PI3K Pathways on PD-L1 Expression in Melanoma
    Atefi, Mohammad
    Avramis, Earl
    Lassen, Amanda
    Wong, Deborah J. L.
    Robert, Lidia
    Foulad, David
    Cerniglia, Michael
    Titz, Bjoern
    Chodon, Thinle
    Graeber, Thomas G.
    Comin-Anduix, Begonya
    Ribas, Antoni
    [J]. CLINICAL CANCER RESEARCH, 2014, 20 (13) : 3446 - 3457
  • [9] Bae Jong-Myon, 2016, J Prev Med Public Health, V49, P97, DOI 10.3961/jpmph.15.068
  • [10] Bang YJ, 2010, LANCET, V376, P1302