Ryoji O, Toma H, Nakazawa H, Goya N, Okumura T, Sonoda T, Kihara T, Tanabe K, Onizuka S, Tomoe H
Department of Urology, Tokyo Women's Medical College, Japan.
Cancer Chemother Pharmacol. 1994;35 Suppl:S60-4. doi: 10.1007/BF00686922.
Intravesical instillation of epirubicin was carried out to investigate the efficacy of this treatment in preventing postoperative recurrence of superficial bladder cancer. The subjects were 100 patients who had been treated with transurethral resection (TUR) for superficial transitional-cell carcinoma of the bladder (classified as primary or recurrent superficial bladder cancer of pathological stage Tis, Ta, or T1 and histological grade G1, G2, or G3) at Tokyo Women's Medical College Hospital and its affiliated hospitals during the 2-year period ranging from April of 1990 through March of 1992. A solution of epirubicin was prepared by dissolving 20 mg in 30 ml physiological saline, and this was instilled into the bladder a total of 17 times during 1 year: once immediately after TUR, once every 2 weeks for the next 4 months, and then once per month for the following 8 months. Thereafter, the course of each patient was followed by performing urinary cytodiagnosis once each month and cystoscopy once every 3 months. Of the 100 patients, 83 were evaluable. The mean duration of follow-up was 461 +/- 222 days, and the recurrence rate was 30.1% (25/83 cases). The recurrence rate determined for primary cases was 19.7%, whereas that recorded for recurrent cases was 61.9%. Adverse effects occurred in 9.3% (9/97) of the patients, but these side effects were mild in severity and the instillation regimen did not have to be discontinued in any of the patients. Analysis of the risk factors for recurrence revealed significantly higher recurrence in the recurrent-patient group and the multiple-tumor group. On the basis of these findings, the authors surmised that when given in an intravesical instillation regimen, epirubicin causes few adverse effects, and its efficacy in the prophylaxis of recurrence of superficial bladder cancer is equivalent to that thus for reported for other drugs. At present, the authors are carrying out a controlled clinical study on epirubicin that takes into account the risk factors for recurrence of superficial bladder cancer.
进行表柔比星膀胱内灌注,以研究该治疗方法预防浅表性膀胱癌术后复发的疗效。研究对象为100例患者,他们于1990年4月至1992年3月的2年期间,在东京女子医科大学医院及其附属医院接受了经尿道切除术(TUR)治疗浅表性膀胱移行细胞癌(病理分期为Tis、Ta或T1,组织学分级为G1、G2或G3的原发性或复发性浅表性膀胱癌)。将20mg表柔比星溶解于30ml生理盐水中配制成溶液,在1年内共向膀胱内灌注17次:TUR术后立即灌注1次,接下来4个月内每2周灌注1次,随后8个月内每月灌注1次。此后,对每位患者每月进行1次尿脱落细胞诊断,每3个月进行1次膀胱镜检查,以跟踪其病情发展。100例患者中,83例可进行评估。平均随访时间为461±222天,复发率为30.1%(25/83例)。原发性病例的复发率为19.7%,而复发性病例的复发率为61.9%。9.3%(9/97)的患者出现了不良反应,但这些副作用程度较轻,所有患者均无需中断灌注方案。对复发危险因素的分析显示,复发性患者组和多肿瘤组的复发率显著更高。基于这些发现,作者推测,表柔比星采用膀胱内灌注方案给药时,不良反应较少,其预防浅表性膀胱癌复发的疗效与其他已报道药物相当。目前,作者正在针对表柔比星开展一项对照临床研究,该研究考虑了浅表性膀胱癌复发的危险因素。