Oncolytic virotherapy for cancer with the adenovirus dl1520 (Onyx-015):: results of Phase I and II trials

被引:130
作者
Kirn, D [1 ]
机构
[1] Hammersmith Hosp, Mol Oncol Unit, Imperial Canc Res Fund, Viral & Genet Therapy Programme, London, England
关键词
adenovirus; cancer; clinical research; gene therapy; viral therapy;
D O I
10.1517/14712598.1.3.525
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Replication-selective viral agents hold promise as a novel cancer treatment platform (virotherapy). dl1520 (Onyx-015, now CI-1042, Pfizer Corp., Groton, CT, USA), an E1B-55kD gene-deleted adenovirus, was the first such genetically engineered agent to be tested in humans. Over 250 cancer patients have now been treated on approximately ten clinical trials (phase I-III). The virus was generally well tolerated at doses of up to 2 x 10(12) particles by intratumoural, intraperitoneal, hepatic arterial and iv. administration; no maximally-tolerated doses were identified following intra-vascular administration. Viral replication was tumour-selective and was documented after administration by all routes; however, viral replication was variable depending on tumour histology. Single agent efficacy has been relatively limited to date (0 - 14% local tumour regression rates). In combination with chemotherapy, however, encouraging antitumoural activity has been demonstrated. These clinical research results demonstrate the potential of this novel treatment platform, as well as the hurdles to be overcome. Novel replication-selective agents with improved potency are being developed.
引用
收藏
页码:525 / 538
页数:14
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共 59 条
  • [1] [Anonymous], P AM SOC CLIN ONCOLO
  • [2] ASADA T, 1974, CANCER, V34, P1907, DOI 10.1002/1097-0142(197412)34:6<1907::AID-CNCR2820340609>3.0.CO
  • [3] 2-4
  • [4] ADENOVIRUS PROTEINS FROM BOTH E1B READING FRAMES ARE REQUIRED FOR TRANSFORMATION OF RODENT CELLS BY VIRAL-INFECTION AND DNA TRANSFECTION
    BARKER, DD
    BERK, AJ
    [J]. VIROLOGY, 1987, 156 (01) : 107 - 121
  • [5] An adenovirus mutant that replicates selectively in p53-deficient human tumor cells
    Bischoff, JR
    Kim, DH
    Williams, A
    Heise, C
    Horn, S
    Muna, M
    Ng, L
    Nye, JA
    SampsonJohannes, A
    Fattaey, A
    McCormick, F
    [J]. SCIENCE, 1996, 274 (5286) : 373 - 376
  • [6] BOVIATSIS EJ, 1994, CANCER RES, V54, P5745
  • [7] Reovirus therapy of tumors with activated Ras pathway
    Coffey, MC
    Strong, JE
    Forsyth, PA
    Lee, PWK
    [J]. SCIENCE, 1998, 282 (5392) : 1332 - 1334
  • [8] Nuclear export of the E1B 55-kDa and E4 34-kDa adenoviral oncoproteins mediated by a rev-like signal sequence
    Dobbelstein, M
    Roth, J
    Kimberly, WT
    Levine, AJ
    Shenk, T
    [J]. EMBO JOURNAL, 1997, 16 (14) : 4276 - 4284
  • [9] Blockage by adenovirus E4orf6 of transcriptional activation by the p53 tumor suppressor
    Dobner, T
    Horikoshi, N
    Rubenwolf, S
    Shenk, T
    [J]. SCIENCE, 1996, 272 (5267) : 1470 - 1473
  • [10] A novel three-pronged approach to kill cancer cells selectively: Concomitant viral, double suicide gene, and radiotherapy
    Freytag, SO
    Rogulski, KR
    Paielli, DL
    Gilbert, JD
    Kim, JH
    [J]. HUMAN GENE THERAPY, 1998, 9 (09) : 1323 - 1333