Clinical and local biological effects of an intraturnoral injection of mda-7 (IL24; INGN 241) in patients with advanced carcinoma:: a phase I study

被引:181
作者
Cunningham, CC
Chada, S
Merritt, JA
Tong, A
Senzer, N
Zhang, Y
Mhashilkar, A
Parker, K
Vukelja, S
Richards, D
Hood, J
Coffee, K
Nemunaitis, J
机构
[1] Mary Crowley Med Res Ctr, Dallas, TX 75246 USA
[2] Introgen Therapeut Inc, Houston, TX 77030 USA
[3] US Oncol, Houston, TX USA
[4] Tyler Canc Ctr, Tyler, TX USA
关键词
mda-7; IL-24; apoptosis; bystander; ER; stress; cytokine; secretion; adenovirus; cancer gene therapy; IL-10; IL-19; IL-20; IL-22; receptor;
D O I
10.1016/j.ymthe.2004.09.019
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
The melanoma differentiation-associated gene-7 (mda-7; approved gene symbol IL24) is a tumor suppressor gene whose expression induces selective apoptosis in tumor cells. To characterize the safety and biologic activity of mda-7 gene transfer, we conducted a phase I trial using intratumoral injections of an adenovirus containing the mda-7 construct (Ad-mda7; INGN 241; 2 x 10(10) to 2 x 10(12) vp) in 28 patients with resectable solid tumors. One hundred percent of injected lesions demonstrated INGN 241 vector transduction, transgenic mRNA, elevated MDA-7 protein, and apoptosis induction, with the highest levels near the injection site. Apoptosis of cells in injected tumors was consistently observed even in heavily pretreated patients. INGN 241 vector DNA and mRNA were detected more than 1 cm from the injection site, whereas MDA-7 protein and bioactivity were more widely distributed. Toxicity attributable to the injections was self-limiting and generally mild; however, one patient experienced a grade 3 SAE possibly related to the study drug. Evidence of clinical activity was found in 44% of lesions with the repeat injection schedule, including complete and partial responses in two melanoma patients. Thus intratumoral administration of INGN 241 is well tolerated, induces apoptosis in a large percentage of tumor cells, and demonstrates evidence of clinically significant activity.
引用
收藏
页码:149 / 159
页数:11
相关论文
共 32 条
  • [11] The melanoma differentiation associated gene mda-7 suppresses cancer cell growth
    Jiang, HP
    Su, ZZ
    Lin, JJ
    Goldstein, NI
    Young, CSH
    Fisher, PB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (17) : 9160 - 9165
  • [12] Adenovirus-mediated mda-7 gene expression radiosensitizes non-small cell lung cancer cells via TP53-independent mechanisms
    Kawabe, S
    Nishikawa, T
    Munshi, A
    Roth, JA
    Chada, S
    Meyn, RE
    [J]. MOLECULAR THERAPY, 2002, 6 (05) : 637 - 644
  • [13] The family of IL-10-related cytokines and their receptors: related, but to what extent?
    Kotenko, SV
    [J]. CYTOKINE & GROWTH FACTOR REVIEWS, 2002, 13 (03) : 223 - 240
  • [14] Phase I trial of adenovirus-mediated p53 gene therapy for recurrent glioma:: Biological and clinical results
    Lang, FF
    Bruner, JM
    Fuller, GN
    Aldape, K
    Prados, MD
    Chang, S
    Berger, MS
    McDermott, MW
    Kunwar, SM
    Junck, LR
    Chandler, W
    Zwiebel, JA
    Kaplan, RS
    Yung, WKA
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (13) : 2508 - 2518
  • [15] Combination therapy of Ad-mda7 and trastuzumab increases cell death in Her-2/neu-overexpressing breast cancer cells
    McKenzie, T
    Liu, Y
    Fanale, M
    Swisher, SG
    Chada, S
    Hunt, KK
    [J]. SURGERY, 2004, 136 (02) : 437 - 442
  • [16] MDA-7 negatively regulates the β-catenin and PI3K signaling pathways in breast and lung tumor cells
    Mhashilkar, AM
    Stewart, AL
    Sieger, K
    Yang, HY
    Khimani, AH
    Ito, I
    Saito, Y
    Hunt, KK
    Grimm, EA
    Roth, JA
    Meyn, RE
    Ramesh, R
    Chada, S
    [J]. MOLECULAR THERAPY, 2003, 8 (02) : 207 - 219
  • [17] Melanoma differentiation associated gene-7 (mda-7): A novel anti-tumor gene for cancer gene therapy
    Mhashilkar, AM
    Schrock, RD
    Hindi, M
    Liao, J
    Sieger, K
    Kourouma, F
    Zou-Yang, XH
    Onishi, E
    Takh, O
    Vedvick, TS
    Fanger, G
    Stewart, L
    Watson, GJ
    Snary, D
    Fisher, PB
    Saeki, T
    Roth, JA
    Ramesh, R
    Chada, S
    [J]. MOLECULAR MEDICINE, 2001, 7 (04) : 271 - 282
  • [18] Prognostic value of K-ras mutations, ras oncoprotein, and c-erb B-2 oncoprotein expression in adenocarcinoma of the lung
    Nemunaitis, J
    Klemow, S
    Tong, A
    Courtney, A
    Johnston, W
    Mack, M
    Taylor, W
    Solano, M
    Stone, M
    Mallams, J
    Mues, G
    [J]. AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1998, 21 (02): : 155 - 160
  • [19] Intravenous infusion of a replication-selective adenovirus (ONYX-015) in cancer patients: safety, feasibility and biological activity
    Nemunaitis, J
    Cunningham, C
    Buchanan, A
    Blackburn, A
    Edelman, G
    Maples, P
    Netto, G
    Tong, A
    Randlev, B
    Olson, S
    Kirn, D
    [J]. GENE THERAPY, 2001, 8 (10) : 746 - 759
  • [20] Adenovirus-mediated mda-7 (IL24) gene therapy suppresses angiogenesis and sensitizes NSCLC xenograft tumors to radiation
    Nishikawa, T
    Ramesh, R
    Munshi, A
    Chada, S
    Meyn, RE
    [J]. MOLECULAR THERAPY, 2004, 9 (06) : 818 - 828