Oncolytic Viruses and Cancer Immunotherapy

被引:24
作者
Malhotra, Jyoti [1 ]
Kim, Edward S. [1 ]
机构
[1] City Hope Comprehens Canc Ctr, Med Oncol Sr Therapeut Res, Pavil Bldg Med Oncol,1500 E Duarte Rd, Duarte, CA 91020 USA
关键词
Oncolytic viruses; Immunotherapy combinations; Clinical trials; CELL LUNG-CANCER; P53; GENE-TRANSFER; PHASE-I; 1ST-LINE CHEMOTHERAPY; SOLID TUMORS; ADENOVIRUS; THERAPY; TG4010; PATHWAYS; REOVIRUS;
D O I
10.1007/s11912-022-01341-w
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of Review Oncolytic viruses (OVs) exert their antitumor effect through selective killing of cancer cells and induction of host anti-tumor immunity. This review aims to summarize the recent and current trials with OVs for the treatment of lung cancer. Recent Findings Several OVs have been developed for the treatment of lung cancer including adenovirus, coxsackievirus B3, reovirus, and vaccinia virus and trials have demonstrated a safe toxicity profile. Early-phase trials in lung cancer with OVs have reported antiviral immune responses and evidence of clinical benefit. However, clinical efficacy of OVs in lung cancer either as monotherapy or in combination with chemotherapy has not been confirmed in larger phase II or III trials. Development of OVs in lung cancer has been limited by difficulty in administering OVs in the tumor directly as well as achieving adequate viral load at all tumor sites with systemically administered OVs. Developing novel combinations with OVs, especially checkpoint inhibitors and other immunotherapeutics, may be a strategy to address the limited success seen thus far. Integrating appropriate biomarker studies and meaningful endpoints in future clinical trials will be imperative. Using novel viral delivery systems in addition to increasing tumor specificity through improved genetic modifications in the OVs are other strategies to improve efficacy.
引用
收藏
页码:19 / 28
页数:10
相关论文
共 74 条
[1]   Phase I Study of Intrapleural Gene-Mediated Cytotoxic Immunotherapy in Patients with Malignant Pleural Effusion [J].
Aggarwal, Charu ;
Haas, Andrew R. ;
Metzger, Susan ;
Aguilar, Laura K. ;
Aguilar-Cordova, Estuardo ;
Manzanera, Andrea G. ;
Gomez-Hernandez, Gregoria ;
Katz, Sharyn I. ;
Alley, Evan W. ;
Evans, Tracey L. ;
Bauml, Joshua M. ;
Cohen, Roger B. ;
Langer, Corey J. ;
Albelda, Steven M. ;
Sterman, Daniel H. .
MOLECULAR THERAPY, 2018, 26 (05) :1198-1205
[2]   The advent of oncolytic virotherapy in oncology: The Rigvir® story [J].
Alberts, Peteris ;
Tilgase, Andra ;
Rasa, Agnija ;
Bandere, Katrina ;
Venskus, Dite .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2018, 837 :117-126
[3]   Talimogene Laherparepvec Improves Durable Response Rate in Patients With Advanced Melanoma [J].
Andtbacka, Robert H. I. ;
Kaufman, Howard L. ;
Collichio, Frances ;
Amatruda, Thomas ;
Senzer, Neil ;
Chesney, Jason ;
Delman, Keith A. ;
Spitler, Lynn E. ;
Puzanov, Igor ;
Agarwala, Sanjiv S. ;
Milhem, Mohammed ;
Cranmer, Lee ;
Curti, Brendan ;
Lewis, Karl ;
Ross, Merrick ;
Guthrie, Troy ;
Linette, Gerald P. ;
Daniels, Gregory A. ;
Harrington, Kevin ;
Middleton, Mark R. ;
Miller, Wilson H., Jr. ;
Zager, Jonathan S. ;
Ye, Yining ;
Yao, Bin ;
Li, Ai ;
Doleman, Susan ;
VanderWalde, Ari ;
Gansert, Jennifer ;
Coffin, Robert S. .
JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (25) :2780-U98
[4]   Updates to the antitumor mechanism of oncolytic virus [J].
Bai, Yang ;
Hui, Peng ;
Du, Xiaoyu ;
Su, Xing .
THORACIC CANCER, 2019, 10 (05) :1031-1035
[5]   Interferon-γ-induced activation of JAK1 and JAK2 suppresses tumor cell susceptibility to NK cells through upregulation of PD-L1 expression [J].
Bellucci, Roberto ;
Martin, Allison ;
Bommarito, Davide ;
Wang, Kathy ;
Hansen, Steen H. ;
Freeman, Gordon J. ;
Ritz, Jerome .
ONCOIMMUNOLOGY, 2015, 4 (06)
[6]   An adenovirus mutant that replicates selectively in p53-deficient human tumor cells [J].
Bischoff, JR ;
Kim, DH ;
Williams, A ;
Heise, C ;
Horn, S ;
Muna, M ;
Ng, L ;
Nye, JA ;
SampsonJohannes, A ;
Fattaey, A ;
McCormick, F .
SCIENCE, 1996, 274 (5286) :373-376
[7]   MECHANISM OF INTERFERON ACTION - ACTIVATION OF THE HUMAN P1/ELF-2-ALPHA-PROTEIN KINASE BY INDIVIDUAL REOVIRUS S-CLASS MESSENGER-RNAS - S1 MESSENGER-RNA IS A POTENT ACTIVATOR RELATIVE TO S4 MESSENGER-RNA [J].
BISCHOFF, JR ;
SAMUEL, CE .
VIROLOGY, 1989, 172 (01) :106-115
[8]  
Bommareddy PK, 2018, NAT REV IMMUNOL, V18, P498, DOI 10.1038/s41577-018-0014-6
[9]   Canadian Cancer Trials Group (CCTG) IND211: A randomized trial of pelareorep (Reolysin) in patients with previously treated advanced or metastatic non-small cell lung cancer receiving standard salvage therapy [J].
Bradbury, Penelope A. ;
Morris, Donald G. ;
Nicholas, Garth ;
Tu, Dongsheng ;
Tehfe, Moustapha ;
Goffin, John R. ;
Shepherd, Frances A. ;
Gregg, Richard W. ;
Rothenstein, Jeffrey ;
Lee, Christoper ;
Kuruvilla, Sara ;
Keith, Bruce D. ;
Torri, Vamsee ;
Blais, Normand ;
Hao, Desiree ;
Korpanty, Grzegorz J. ;
Goss, Glenwood ;
Melosky, Barbara L. ;
Mates, Mihaela ;
Leighl, Natasha ;
Ayoub, Jean-Pierre ;
Sederias, Joana ;
Feilotter, Harriet ;
Seymour, Lesley ;
Laurie, Scott A. .
LUNG CANCER, 2018, 120 :142-148
[10]   Potentiating Cancer Immunotherapy Using an Oncolytic Virus [J].
Bridle, Byram W. ;
Stephenson, Kyle B. ;
Boudreau, Jeanette E. ;
Koshy, Sandeep ;
Kazdhan, Natasha ;
Pullenayegum, Eleanor ;
Brunelliere, Jerome ;
Bramson, Jonathan L. ;
Lichty, Brian D. ;
Wan, Yonghong .
MOLECULAR THERAPY, 2010, 18 (08) :1430-1439