The advent of oncolytic virotherapy in oncology: The Rigvir® story

被引:112
作者
Alberts, Peteris [1 ]
Tilgase, Andra [1 ]
Rasa, Agnija [1 ]
Bandere, Katrina [1 ]
Venskus, Dite [1 ]
机构
[1] Int Virotherapy Ctr, Teatra Iela 9-9, LV-1050 Riga, Latvia
关键词
ECHO-7; virus; Melanoma; Oncotropism; Oncolytic; Rigvir; Virotherapy; DECAY-ACCELERATING FACTOR; NEWCASTLE-DISEASE-VIRUS; CONTINUING SURVEILLANCE; RHABDOMYOSARCOMA CELLS; ECHOVIRUS INFECTION; HISTIOCYTIC SARCOMA; ROSETTE FORMATION; CANCER-TREATMENT; FACTOR CD55; MELANOMA;
D O I
10.1016/j.ejphar.2018.08.042
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Oncolytic viruses are a fast-developing cancer treatment field. Numerous viruses have been tested in clinical trials and three are approved. The first, Rigvir, is an immunomodulator with anti-tumour effect for treatment of melanoma, local treatment of skin and subcutaneous metastases of melanoma, for prevention of relapse and metastasis after radical surgery registered in Latvia, Georgia, Armenia and Uzbekistan. The aim of the present review is to summarize the development of Rigvir. Approximately 60 viruses were screened preclinically. Clinical safety and efficacy trials were with 5 oncolytic enteroviruses. Safety of the selected and melanoma-adapted ECHO-7 virus Rigvir was tested in over 180 patients with no severe adverse events observed. Pre-registration efficacy studies involved over 700 cancer patients: over 540 melanoma patients, and patients with late stage stomach (ca. 90), colorectal cancer (ca. 60), and other cancers. Patients were treated with Rigvir for 3 years after surgery and compared to immunotherapy: 3- and 5-year overall survival appeared to be increased in Rigvir treated patients. In post-marketing retrospective studies, Rigvir-treated stage II melanoma patients showed a 6.67-fold decreased risk for disease progression in comparison to those that had been observed according to guidelines, and stage IB and stage II melanoma patients that had received Rigvir therapy had 4.39-6.57-fold lower mortality. The results are confirmed and extended by case reports. Several immunological markers have been measured. In conclusion, Rigvir is an oncotropic and oncolytic virus for treatment of melanoma; the results will be confirmed and updated by modern clinical studies.
引用
收藏
页码:117 / 126
页数:10
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共 126 条
  • [11] [Anonymous], P LATV ACAD SCI
  • [12] ASADA T, 1974, CANCER, V34, P1907, DOI 10.1002/1097-0142(197412)34:6<1907::AID-CNCR2820340609>3.0.CO
  • [13] 2-4
  • [14] Austin F C, 1979, Adv Cancer Res, V30, P301, DOI 10.1016/S0065-230X(08)60900-8
  • [15] Oncolytic viruses as therapeutic cancer vaccines
    Bartlett, David L.
    Liu, Zuqiang
    Sathaiah, Magesh
    Ravindranathan, Roshni
    Guo, Zongbi
    He, Yukai
    Guo, Zong Sheng
    [J]. MOLECULAR CANCER, 2013, 12
  • [16] DECAY-ACCELERATING FACTOR (CD55), A GLYCOSYLPHOSPHATIDYLINOSITOL-ANCHORED COMPLEMENT REGULATORY PROTEIN, IS A RECEPTOR FOR SEVERAL ECHOVIRUSES
    BERGELSON, JM
    CHAN, M
    SOLOMON, KR
    STJOHN, NF
    LIN, HM
    FINBERG, RW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (13) : 6245 - 6248
  • [17] ROSETTE FORMATION BETWEEN HUMAN LYMPHOCYTES AND SHEEP ERYTHROCYTES - INHIBITION OF ROSETTE FORMATION BY SPECIFIC GLYCOPEPTIDES
    BOLDT, DH
    ARMSTRONG, JP
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1976, 57 (04) : 1068 - 1078
  • [18] Talimogene Laherparepvec (T-VEC) and Other Oncolytic Viruses for the Treatment of Melanoma
    Bommareddy, Praveen K.
    Patel, Anand
    Hossain, Saamia
    Kaufman, Howard L.
    [J]. AMERICAN JOURNAL OF CLINICAL DERMATOLOGY, 2017, 18 (01) : 1 - 15
  • [19] Brokane L., STAT ANAL CHAN UNPUB, P1
  • [20] Bruvere R., 2006, MELANOMA RES, V16