Onrust S V, Wiseman L R, Goa K L
Adis International Limited, Mairangi Bay, Auckland, New Zealand.
Drugs Aging. 1999 Oct;15(4):307-33. doi: 10.2165/00002512-199915040-00006.
The anthracycline epirubicin has been investigated for intravesical use in patients with superficial bladder cancer. In multicentre, randomised trials, prophylaxis with intravesical epirubicin 30 to 80 mg after transurethral resection (TUR) was more effective than no prophylaxis in the prevention of disease recurrence. Intravesical prophylaxis with epirubicin was as effective as that with equivalent dosages of doxorubicin after TUR. Data are conflicting concerning the relative efficacy of intravesical epirubicin and bacillus Calmette-Guerin (BCG) in patients at intermediate risk of recurrence after TUR, but epirubicin was less effective than BCG in those at high risk. The efficacy and tolerability of prophylaxis with epirubicin relative to that with mitomycin is not yet established. The efficacy of epirubicin as prophylaxis after TUR in combination with BCG or interferon-alpha-2b, or as treatment in patients with superficial bladder cancer has been evaluated in small, noncomparative trials, but requires clarification. Adverse events associated with intravesical epirubicin were generally mild and transient. The most common adverse events were localised to the bladder (cystitis, haematuria and urinary tract infection). Systemic adverse events (cardiac, haematological or related to hypersensitivity) were not reported in many trials of intravesical epirubicin, and when reported generally occurred in < or =5% of patients who received the drug. Intravesical epirubicin was generally tolerated as well as intravesical doxorubicin and was associated with a lower incidence of mild chemical cystitis in 1 clinical trial. The incidence of adverse events associated with intravesical epirubicin was markedly lower than that associated with intravesical BCG.
Intravesical epirubicin has shown efficacy in preventing disease recurrence after TUR of superficial bladder cancer. In comparison with equivalent dosages of doxorubicin, the efficacy of epirubicin for this indication is generally similar, and the tolerability profile may be more favourable. Epirubicin is less effective than BCG as intravesical prophylaxis in patients at high risk of recurrence after TUR; the relative efficacy of epirubicin and BCG after TUR in patients at intermediate risk is not yet clear. Intravesical epirubicin is generally tolerated better than BCG. Intravesical epirubicin may be used as prophylaxis after TUR in patients who are at low or intermediate risk of recurrence of superficial bladder cancer.
已对蒽环类药物表柔比星用于浅表性膀胱癌患者的膀胱内灌注进行了研究。在多中心随机试验中,经尿道切除(TUR)后膀胱内灌注30至80毫克表柔比星预防疾病复发比不进行预防更有效。TUR后膀胱内灌注表柔比星预防疾病复发的效果与等量多柔比星相同。关于TUR后复发风险中等的患者膀胱内灌注表柔比星与卡介苗(BCG)的相对疗效的数据存在冲突,但在复发风险高的患者中,表柔比星的效果不如BCG。相对于丝裂霉素,表柔比星预防疾病复发的疗效和耐受性尚未确定。在小型非对照试验中评估了表柔比星在TUR后与BCG或干扰素-α-2b联合用于预防疾病复发或用于浅表性膀胱癌患者治疗的疗效,但仍需进一步明确。与膀胱内灌注表柔比星相关的不良事件一般较轻且为一过性。最常见的不良事件局限于膀胱(膀胱炎、血尿和尿路感染)。在许多膀胱内灌注表柔比星的试验中未报告全身性不良事件(心脏、血液学或与超敏反应相关的不良事件),报告时一般在接受该药物治疗的患者中发生率≤5%。膀胱内灌注表柔比星的耐受性一般与膀胱内灌注多柔比星相同,且在1项临床试验中轻度化学性膀胱炎的发生率较低。与膀胱内灌注表柔比星相关的不良事件发生率明显低于与膀胱内灌注BCG相关的不良事件发生率。
膀胱内灌注表柔比星已显示出预防浅表性膀胱癌TUR后疾病复发的疗效。与等量多柔比星相比,表柔比星在该适应证上的疗效一般相似,且耐受性可能更好。在TUR后复发风险高的患者中,膀胱内灌注表柔比星预防疾病复发的效果不如BCG;TUR后复发风险中等的患者中表柔比星与BCG的相对疗效尚不清楚。膀胱内灌注表柔比星的耐受性一般优于BCG。膀胱内灌注表柔比星可用于浅表性膀胱癌复发风险低或中等的患者TUR后的预防。