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.
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收藏
页码:149 / 159
页数:11
相关论文
共 32 条
  • [1] Adenoviral transfer of mda-7 leads to BAX up-regulation and apoptosis in mesothelioma cells, and is abrogated by over-expression of BCL-XL
    Cao, XX
    Mohuiddin, I
    Chada, S
    Mhashilkar, AM
    Ozvaran, MK
    McConkey, DJ
    Miller, SD
    Daniel, JC
    Smythe, WR
    [J]. MOLECULAR MEDICINE, 2002, 8 (12) : 869 - 876
  • [2] The protein product of the tumor suppressor gene, melanoma differentiation-associated gene 7, exhibits immunostimulatory activity and is designated IL-24
    Caudell, EG
    Mumm, JB
    Poindexter, N
    Ekmekcioglu, S
    Mhashilkar, AM
    Yang, XHH
    Retter, MW
    Hill, P
    Chada, S
    Grimm, EA
    [J]. JOURNAL OF IMMUNOLOGY, 2002, 168 (12) : 6041 - 6046
  • [3] Chada S, 2003, CURR OPIN MOL THER, V5, P463
  • [4] MDA-7/IL-24 is a unique cytokine-tumor suppressor in the IL-10 Family
    Chada, S
    Sutton, RB
    Ekmekcioglu, S
    Ellerhorst, J
    Mumm, JB
    Leitner, WW
    Yang, HY
    Sahin, AA
    Hunt, KK
    Fuson, KL
    Poìndexter, N
    Roth, JA
    Ramesh, R
    Grimm, EA
    Mhashilkar, AM
    [J]. INTERNATIONAL IMMUNOPHARMACOLOGY, 2004, 4 (05) : 649 - 667
  • [5] CHADA S, 2004, IN PRESS MOL THER
  • [6] Ekmekcioglu S, 2003, MOL CANCER THER, V2, P9
  • [7] Down-regulated melanoma differentiation associated gene (MDA-7) expression in human melanomas
    Ekmekcioglu, S
    Ellerhorst, J
    Mhashilkar, AM
    Sahin, AA
    Read, CM
    Prieto, VG
    Chada, S
    Grimm, EA
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2001, 94 (01) : 54 - 59
  • [8] Loss of MDA-7 expression with progression of melanoma
    Ellerhorst, JA
    Prieto, VG
    Ekmekcioglu, S
    Broemeling, L
    Yekell, S
    Chada, S
    Grimm, EA
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (04) : 1069 - 1074
  • [9] Fisher PB, 2003, CANCER BIOL THER, V2, pS23
  • [10] Jiang HP, 1995, ONCOGENE, V11, P2477