Losa A, Hurle R, Lembo A
Division of Urology, Ospedali Riuniti di Bergamo, Italy.
J Urol. 2000 Jan;163(1):68-71; discussion 71-2.
Bacillus Calmette-Guerin (BCG) is standard treatment for carcinoma in situ of the bladder. However, its long-term effectiveness is still debated.
From January 1987 to January 1995, 70 consecutive patients with primary or secondary carcinoma in situ with or without concomitant solitary or multifocal papillary tumor were treated with weekly instillations of 75 mg. Pasteur strain BCG for 6 weeks after histological diagnosis. An additional induction course was given to patients with relapse. Tumor-free patients were given a maintenance course of monthly instillations for 12 months.
At the end of induction course 1, 56 of the 70 patients (80%) were tumor-free. Of 14 patients given induction course 2, 9 had a complete response (64.2%). A total of 65 patients (92.8%) were disease-free after 1 or 2 courses and given the maintenance course. Median followup for disease-free patients was 74 months (range 17 to 134). Subsequently 50 patients (71.4%) were disease-free, 12 (17.1%) had recurrence and 8 (11.4%) had progression. Mean time was 18 months (range 6 to 69) to treatment failure and 13 months (range 7 to 53) to progression. Of the patients 1 died of disease and 10 of other causes. Crude survival was 84.2%, disease specific mortality 1.4% and nondisease specific mortality 14.2%. The risk of treatment failure was significantly greater for carcinoma in situ associated with stage T1 papillary tumor (p = 0.0001) or severe dysplasia (p = 0.0005), and the risk of disease progression was significantly greater for carcinoma in situ associated with stage T1 papillary tumor (p = 0.0001). The drug was well tolerated with few side effects.
Intravesical BCG is the best available conservative therapy for patients with carcinoma in situ of the bladder. Low dose BCG is similarly effective, with a lower incidence of side effects and long lasting positive outcome.
卡介苗(BCG)是膀胱原位癌的标准治疗方法。然而,其长期疗效仍存在争议。
1987年1月至1995年1月,连续70例原发性或继发性原位癌患者,伴或不伴有孤立性或多灶性乳头状肿瘤,在组织学诊断后每周膀胱灌注75mg卡介苗巴斯德菌株,共6周。复发患者给予额外的诱导疗程。无瘤患者给予每月一次的维持疗程,共12个月。
在诱导疗程1结束时,70例患者中有56例(80%)无肿瘤。在接受诱导疗程2的14例患者中,9例完全缓解(64.2%)。1或2个疗程后,共有65例患者(92.8%)无疾病,并接受维持疗程。无疾病患者的中位随访时间为74个月(范围17至134个月)。随后,50例患者(71.4%)无疾病,12例(17.1%)复发,8例(11.4%)进展。治疗失败的平均时间为18个月(范围6至69个月),进展的平均时间为13个月(范围7至53个月)。患者中1例死于疾病,10例死于其他原因。粗生存率为84.2%,疾病特异性死亡率为1.4%,非疾病特异性死亡率为14.2%。与T1期乳头状肿瘤相关的原位癌(p = 0.0001)或重度发育异常(p = 0.0005)患者治疗失败的风险显著更高,与T1期乳头状肿瘤相关的原位癌患者疾病进展的风险显著更高(p = 0.0001)。该药物耐受性良好,副作用较少。
膀胱内灌注卡介苗是膀胱原位癌患者可用的最佳保守治疗方法。低剂量卡介苗同样有效,副作用发生率较低,且有持久的阳性结果。