Use of monitoring levels of soluble forms of cytokeratin 18 in the urine of patients with superficial bladder cancer following intravesical Ad-IFNα/Syn3 treatment in a phase 1 study

被引:11
作者
Benedict, W. F. [1 ]
Fisher, M. [2 ]
Zhang, X-Q [1 ]
Yang, Z. [1 ]
Munsell, M. F. [3 ]
Dinney, C. N. P. [2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Box 1374,1515 Holcombe Blvd, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Urol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
关键词
Adenoviral-mediated interferon alpha treatment; urine cytokeratin 18 levels; bladder cancer; phase I study; ADENOVIRAL-MEDIATED INTERFERON; OVERCOMES RESISTANCE; TUMOR;
D O I
10.1038/cgt.2014.1
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
A phase I study using intravesical Ad-IFN alpha Syn3 for patients with bacillus Calmette-Guerin-resistant superficial bladder cancer showed a complete remission (CR) of 43% at 90 days after treatment with high levels of interferon-alpha (IFN alpha) being produced. Ad-IFN alpha kills bladder cancer cells by two apoptotic and one necrotic mechanism that can be measured by soluble forms of cytokeratin 18 (CK18) using M30 and M65 ELISAs, assays for caspase-cleaved (apoptotic) and uncleaved (necrotic) cell death, respectively. Therefore, we determined whether M30 and M65 levels in the urine after treatment could document all three mechanisms of cancer cell kill and also predict having a CR. High levels of both M30 and M65 were found in all patients within 24h after treatment with all three types of cancer cell death occurring. Moreover, the return of both M30 and M65 levels in the urine to normal levels within 5 days or more after treatment was strongly associated with obtaining a CR (P=0.003). This is the first time that such assays have been used to study response to therapy in the urine of patients with bladder cancer and in the future may prove valuable in predicting clinical outcome.
引用
收藏
页码:91 / 94
页数:4
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