The Role of Oncolytic Viruses in the Treatment of Melanoma

被引:35
作者
Bayan, Claire-Audrey Y. [1 ]
Lopez, Adriana T. [1 ]
Gartrell, Robyn D. [2 ]
Komatsubara, Kimberly M. [2 ]
Bogardus, Margaret [1 ]
Rao, Nisha [2 ]
Chen, Cynthia [1 ]
Hart, Thomas D. [3 ]
Enzler, Thomas [2 ]
Rizk, Emanuelle M. [2 ]
Pradhan, Jaya Sarin [4 ]
Marks, Douglas K. [2 ]
Geskin, Larisa J. [5 ]
Saenger, Yvonne M. [2 ]
机构
[1] Columbia Univ, Med Ctr, New York, NY 10032 USA
[2] Columbia Univ, Med Ctr, Dept Med, Div Hematol Oncol, 161 Ft Washington Ave, New York, NY 10032 USA
[3] Columbia Univ, Columbia Coll, New York, NY 10027 USA
[4] Columbia Univ, Med Ctr, Dept Pathol, New York, NY 10032 USA
[5] Columbia Univ, Med Ctr, Dept Dermatol, New York, NY 10032 USA
关键词
Oncolytic virus; Oncolytic viral therapy; Melanoma; Immunotherapy; Talimogene laherparepvec (T-VEC); Tumor microenvironment; Biosafety; Combination therapy; HERPES-SIMPLEX-VIRUS; NEWCASTLE-DISEASE VIRUS; PHASE-I TRIAL; COSTIMULATORY MOLECULES; TALIMOGENE LAHERPAREPVEC; MALIGNANT-MELANOMA; MEASLES-VIRUS; TUMOR; EXPRESSION; TYPE-1;
D O I
10.1007/s11912-018-0729-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of Review Oncolytic virotherapy is a new approach to the treatment of cancer and its success in the treatment of melanoma represents a breakthrough in cancer therapeutics. This paper provides a review of the current literature on the use of oncolytic viruses (OVs) in the treatment of melanoma. Recent Findings Talimogene laherparepvec (T-VEC) is the first OV approved for the treatment of melanoma and presents new challenges as it enters the clinical setting. Several other OVs are at various stages of clinical and pre-clinical development for the treatment of melanoma. Reports from phase Ib-III clinical trials combining T-VEC with checkpoint blockade are encouraging and demonstrate potential added benefit of combination immunotherapy. Summary OVs have recently emerged as a standard treatment option for patients with advanced melanoma. Several OVs and therapeutic combinations are in development. Immunooncolytic virotherapy combined with immune checkpoint inhibitors is promising for the treatment of advanced melanoma.
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页数:14
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共 85 条
[71]   Defining the role of the tumor vasculature in antitumor immunity and immunotherapy [J].
Schaaf, Marco B. ;
Garg, Abhishek D. ;
Agostinis, Patrizia .
CELL DEATH & DISEASE, 2018, 9
[72]   Phase II Clinical Trial of a Granulocyte-Macrophage Colony-Stimulating Factor-Encoding, Second-Generation Oncolytic Herpesvirus in Patients With Unresectable Metastatic Melanoma [J].
Senzer, Neil N. ;
Kaufman, Howard L. ;
Amatruda, Thomas ;
Nemunaitis, Mike ;
Reid, Tony ;
Daniels, Gregory ;
Gonzalez, Rene ;
Glaspy, John ;
Whitman, Eric ;
Harrington, Kevin ;
Goldsweig, Howard ;
Marshall, Tracey ;
Love, Colin ;
Coffin, Robert ;
Nemunaitis, John J. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (34) :5763-5771
[73]   Systemic therapy of malignant human melanoma tumors by a common cold-producing enterovirus, coxsackievirus A21 [J].
Shafren, DR ;
An, GG ;
Nguyen, T ;
Newcombe, NG ;
Haley, ES ;
Beagley, L ;
Johansson, ES ;
Hersey, P ;
Barry, RD .
CLINICAL CANCER RESEARCH, 2004, 10 (01) :53-60
[74]   Effect of hypoxia on Ad5 infection, transgene expression and replication [J].
Shen, BH ;
Hermiston, TW .
GENE THERAPY, 2005, 12 (11) :902-910
[75]   A phase I trial of intravenous CG7870, a replication-selective, prostate-specific antigen-targeted oncolytic adenovirus, for the treatment of hormone-refractory, metastatic prostate cancer [J].
Small, Eric J. ;
Carducci, Michael A. ;
Burke, James M. ;
Rodriguez, Ron ;
Fong, Lawrence ;
van Ummersen, Lynn ;
Yu, D. C. ;
Aimi, Junko ;
Ando, Dale ;
Working, Peter ;
Kirn, David ;
Wilding, George .
MOLECULAR THERAPY, 2006, 14 (01) :107-117
[76]   Oncolytic viral therapy using a spontaneously generated herpes simplex virus type 1 variant for disseminated peritoneal tumor in immunocompetent mice [J].
Takakuwa, H ;
Goshima, R ;
Nozawa, N ;
Yoshikawa, T ;
Kimata, H ;
Nakao, A ;
Nawa, A ;
Kurata, T ;
Sata, T ;
Nishiyama, Y .
ARCHIVES OF VIROLOGY, 2003, 148 (04) :813-825
[77]   Tumor growth inhibition by intratumoral inoculation of defective herpes simplex virus vectors expressing granulocyte-macrophage colony-stimulating factor [J].
Toda, M ;
Martuza, RL ;
Rabkin, SD .
MOLECULAR THERAPY, 2000, 2 (04) :324-329
[78]   Determination and analysis of the DNA sequence of highly attenuated herpes simplex virus type 1 mutant HF10, a potential oncolytic virus [J].
Ushijima, Yoko ;
Luo, Chenhong ;
Goshima, Fumi ;
Yamauchi, Yohei ;
Kimura, Hiroshi ;
Nishiyama, Yukihiro .
MICROBES AND INFECTION, 2007, 9 (02) :142-149
[79]   Regulation of dendritic cell development by GM-CSF: molecular control and implications for immune homeostasis and therapy [J].
van de Laar, Lianne ;
Coffer, Paul J. ;
Woltman, Andrea M. .
BLOOD, 2012, 119 (15) :3383-3393
[80]   A Phase I Study of Intravenous Oncolytic Reovirus Type 3 Dearing in Patients with Advanced Cancer [J].
Vidal, Laura ;
Pandha, Hardev S. ;
Yap, Timothy A. ;
White, Christine L. ;
Twigger, Katie ;
Vile, Richard G. ;
Melcher, Alan ;
Coffey, Matt ;
Harrington, Kevin J. ;
DeBono, Johann S. .
CLINICAL CANCER RESEARCH, 2008, 14 (21) :7127-7137