Clinical research results with dl1520 (Onyx-015), a replication-selective adenovirus for the treatment of cancer: what have we learned?

被引:293
作者
Kirn, D [1 ]
机构
[1] Hammersmith Hosp, Imperial Coll Sch Med, Imperial Canc Res Fund,Med Oncol Unit, Viral & Genet Therapy Programme, London W12 0NN, England
关键词
clinical trials; adenovirus; cancer; dl1520; oncolytic;
D O I
10.1038/sj.gt.3301377
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Replication-selective microbial agents hold promise as a novel cancer treatment platform, dl1520 (Onyx-015), an E1B-55 kD gene-deleted adenovirus, was the first such genetically engineered agent to be tested in humans. Over 200 cancer patients have been treated to date on over 10 clinical trials (phases I-III). The virus was generally well-tolerated at doses of up to 2 x 10(12) particles by intratumoral, intraperitoneal, hepatic arterial and intravenous administration; no maximally tolerated doses were identified by any route of administration. Viral replication was tumor-selective, and was documented after administration by all routes; replication was generally transient (<10 days), however, and was variable depending on tumor histology. Single agent efficacy has been limited to date (0-14% local tumor regression rates). In combination with chemotherapy, however, encouraging antitumoral 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 needed.
引用
收藏
页码:89 / 98
页数:10
相关论文
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