Repeated intravesical instillations of an adenoviral vector in patients with locally advanced bladder cancer:: A phase I study of p53 gene therapy

被引:104
作者
Pagliaro, LC
Keyhani, A
Williams, D
Woods, D
Liu, BS
Perrotte, P
Slaton, JW
Merritt, JA
Grossman, HB
Dinney, CP
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Urol, Houston, TX 77030 USA
[3] Introgen Therapeut Inc, Houston, TX USA
关键词
D O I
10.1200/JCO.2003.09.138
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We investigated the feasibility, safety, and biologic activity of adenovirus-mediated p53 gene transfer in patients with locally advanced bladder cancer. Patients and Methods: Patients with measurable, locally advanced transitional-cell carcinoma of the bladder who were not candidates for cystectomy were eligible. On a 28-day cycle, intravesical instillations of INGN 201 (Ad5CMV-p53) were administered on days 1 and 4 at three dose levels (10(10) particles to 10(12) particles) or on either 4 or 8 consecutive days at a single dose level (10(12) particles). Results: Thirteen patients received a total of 22 courses without dose-limiting toxicity. Specific transgene expression was detected by reverse transcriptase polymerase chain reaction in bladder biopsy tissue from two of seven assessable patients. There were no changes in p53, p21(waf1/cip1), or box protein levels in bladder epithelium evident from immunohistochemical analysis of 11 assessable patients. Outpatient administration of multiple courses was feasible and well tolerated. A patient with advanced superficial bladder cancer showed evidence of tumor response. Conclusion: Intravesical instillation of Ad5CMV-p53 is safe, feasible, and biologically active when administered in multiple doses to patients with bladder cancer. Observations from this study indicate that this treatment has an antitumor effect in superficial transitional-cell carcinoma. improvements in the efficiency of gene transfer and the levels of gene expression are required to develop more effective gene therapy for bladder cancer.
引用
收藏
页码:2247 / 2253
页数:7
相关论文
共 25 条
[1]  
AYALA AG, 1989, PATHOLOGY URINARY BL, P65
[2]   Adenovirus-mediated p53 gene transfer in patients with advanced recurrent head and neck squamous cell carcinoma [J].
Clayman, GL ;
El-Naggar, AK ;
Lippman, SM ;
Henderson, YC ;
Frederick, M ;
Merritt, JA ;
Zumstein, LA ;
Timmons, TM ;
Liu, TJ ;
Ginsberg, L ;
Roth, JA ;
Hong, WK ;
Bruso, P ;
Goepfert, H .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (06) :2221-2232
[3]   Identification of polyamides that enhance adenovirus-mediated gene expression in the urothelium [J].
Conner, RJ ;
Engler, H ;
Machemer, T ;
Philopena, JM ;
Horn, MT ;
Sutjipto, S ;
Maneval, DC ;
Youngster, S ;
Chan, TM ;
Bausch, J ;
McAuliffe, JP ;
Hindsgaul, O ;
Nagabhushan, TL .
GENE THERAPY, 2001, 8 (01) :41-48
[4]   ACCUMULATION OF NUCLEAR P53 AND TUMOR PROGRESSION IN BLADDER-CANCER [J].
ESRIG, D ;
ELMAJIAN, D ;
GROSHEN, S ;
FREEMAN, JA ;
STEIN, JP ;
CHEN, SC ;
NICHOLS, PW ;
SKINNER, DG ;
JONES, PA ;
COTE, RJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (19) :1259-1264
[5]  
Grossman H. Barton, 1997, P269
[6]  
Haviv YS, 2002, CANCER RES, V62, P4273
[7]  
Herr Harry W., 1997, P273
[8]   Successful adenovirus-mediated wild-type p53 gene transfer in patients with bladder cancer by intravesical vector instillation [J].
Kuball, J ;
Wen, SF ;
Leissner, J ;
Atkins, D ;
Meinhardt, P ;
Quijano, E ;
Engler, H ;
Hutchins, B ;
Maneval, DC ;
Grace, MJ ;
Fritz, MA ;
Störkel, S ;
Thüroff, JW ;
Huber, C ;
Schuler, M .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (04) :957-965
[9]  
Li YM, 1999, CANCER RES, V59, P325
[10]   Integrated therapy for locally advanced bladder cancer: Final report of a randomized trial of cystectomy plus adjuvant M-VAC versus cystectomy with both preoperative and postoperative M-VAC [J].
Millikan, R ;
Dinney, C ;
Swanson, D ;
Sweeney, P ;
Ro, JY ;
Smith, TL ;
Williams, D ;
Logothetis, C .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (20) :4005-4013