L G Gomella, D E McGinnis, E C Lattime, K Butler, M Baltish, I Thompson, M E Marshall
{"title":"Treatment of transitional cell carcinoma of the bladder with intravesical interleukin-2: a pilot study.","authors":"L G Gomella, D E McGinnis, E C Lattime, K Butler, M Baltish, I Thompson, M E Marshall","doi":"10.1089/cbr.1993.8.223","DOIUrl":null,"url":null,"abstract":"<p><p>Human recombinant interleukin-2 (rIL-2) administered systemically can mediate the regression of solid tumors in some patients. IL-2 has been detected in the bladder effluent from patients treated with intravesical BCG for transitional cell carcinoma of the bladder (TCC), suggesting that IL-2 may be an effector molecule in the mechanism of action of BCG. The purpose of the pilot study was to determine the response rate, duration of response and toxicity of rIL-2 (Cetus) administered intravesically to previously untreated patients and patients who had failed prior intravesical therapy with other agents. Fourteen patients with biopsy proven transitional cell carcinoma (13 Stage TIS/Ta/T1, 1 Stage T2) were treated with 8 weekly instillations of 12 x 10(6) IU of rIL-2. An index lesion was followed with cystoscopy, biopsy and cytology at three months, with identical follow up every three months thereafter if a response was noted in the index lesion at the first evaluation. There were 3 complete responses (duration of response measured from start of treatment to date of progression) of 9+, 3, 9 months; one patient with TIS, and 2 patients with Ta disease. There were 11 non-responders for an overall response rate of 21%. One patient with extensive CIS had a dramatic partial response and was converted to a complete response with a second 8-week course of rIL-2. All of the complete responders had failed prior intravesical therapy with standard agents. Toxicity from rIL-2 given intravesically was minimal. One patient reported malaise for 24 hours after each treatment and two patients developed asymptomatic lower UTIs.(ABSTRACT TRUNCATED AT 250 WORDS)</p>","PeriodicalId":79322,"journal":{"name":"Cancer biotherapy","volume":"8 3","pages":"223-7"},"PeriodicalIF":0.0000,"publicationDate":"1993-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/cbr.1993.8.223","citationCount":"19","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer biotherapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1089/cbr.1993.8.223","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 19
Abstract
Human recombinant interleukin-2 (rIL-2) administered systemically can mediate the regression of solid tumors in some patients. IL-2 has been detected in the bladder effluent from patients treated with intravesical BCG for transitional cell carcinoma of the bladder (TCC), suggesting that IL-2 may be an effector molecule in the mechanism of action of BCG. The purpose of the pilot study was to determine the response rate, duration of response and toxicity of rIL-2 (Cetus) administered intravesically to previously untreated patients and patients who had failed prior intravesical therapy with other agents. Fourteen patients with biopsy proven transitional cell carcinoma (13 Stage TIS/Ta/T1, 1 Stage T2) were treated with 8 weekly instillations of 12 x 10(6) IU of rIL-2. An index lesion was followed with cystoscopy, biopsy and cytology at three months, with identical follow up every three months thereafter if a response was noted in the index lesion at the first evaluation. There were 3 complete responses (duration of response measured from start of treatment to date of progression) of 9+, 3, 9 months; one patient with TIS, and 2 patients with Ta disease. There were 11 non-responders for an overall response rate of 21%. One patient with extensive CIS had a dramatic partial response and was converted to a complete response with a second 8-week course of rIL-2. All of the complete responders had failed prior intravesical therapy with standard agents. Toxicity from rIL-2 given intravesically was minimal. One patient reported malaise for 24 hours after each treatment and two patients developed asymptomatic lower UTIs.(ABSTRACT TRUNCATED AT 250 WORDS)
人重组白细胞介素-2 (il -2)系统给药可介导部分患者实体瘤的消退。膀胱内卡介苗治疗膀胱移行细胞癌(TCC)患者膀胱流出液中检测到IL-2,提示IL-2可能是卡介苗作用机制中的一个效应分子。该初步研究的目的是确定il -2 (Cetus)静脉内给药的反应率、反应持续时间和毒性,这些患者之前未经治疗,之前用其他药物进行静脉内治疗失败。14例活检证实为移行细胞癌的患者(13例为TIS/Ta/T1期,1例为T2期)接受8周12 × 10(6) IU il -2滴注治疗。3个月时对指标病变进行膀胱镜检查、活检和细胞学检查,如果在第一次评估时发现指标病变有反应,则此后每3个月进行一次相同的随访。有3个完全缓解(从治疗开始到进展日期测量的缓解持续时间),分别为9+、3、9个月;1例为TIS, 2例为Ta。有11例无反应,总有效率为21%。一名患有广泛CIS的患者出现了戏剧性的部分缓解,并通过第二个8周的rIL-2疗程转化为完全缓解。所有完全应答者先前使用标准药物进行膀胱内治疗失败。il -2静脉给予的毒性很小。1例患者在每次治疗后24小时报告不适,2例患者出现无症状的下尿路感染。(摘要删节250字)