Gårdmark Truls, Jahnson Staffan, Wahlquist Rolf, Wijkström Hans, Malmström Per-Uno
Department of Urology, Surgical Sciences, Uppsala, Sweden.
BJU Int. 2007 Apr;99(4):817-20. doi: 10.1111/j.1464-410X.2006.06706.x. Epub 2007 Jan 22.
To report the 10-year follow-up of a study randomizing between instillations of bacillus Calmette-Guérin (BCG) and mitomycin-C (MMC) for treating high-risk and not muscle-invasive urinary bladder cancer to assess progression, the need for more aggressive treatment and survival (cancer-specific and overall), as many of the published studies comparing different treatments for disease that is not muscle-invasive have a short follow-up.
Between 1987 and 1992, 261 patients were included; they had frequently recurring Ta/T1G1-G2, T1G3 or primary Tis-dysplasia. The patients were randomized to treatment with either 40 mg of MMC or 120 mg of BCG (Danish strain 1331) given weekly for 6 weeks, then monthly up to a year and finally every third month for a further year. The 250 evaluable patients were followed using hospital files and national registers on causes of death.
The median follow-up for survivors was 123 months. The disease progressed in 58 (23%) of the patients, 34 in the MMC group and 24 in the BCG group (P = 0.26). Of the 140 patients who died, 68 were in the BCG and 72 in the MMC group (log-rank P = 0.98); most (95, 68%) died from other causes.
Based on the follow-up of the present patients it cannot be concluded that the drugs originally administered, MMC or BCG, differed in their effect on progression, need for subsequent treatment or survival.
报告一项针对高危非肌层浸润性膀胱癌患者,随机接受卡介苗(BCG)和丝裂霉素-C(MMC)膀胱灌注治疗的10年随访研究结果,以评估疾病进展情况、是否需要更积极的治疗以及生存率(癌症特异性生存率和总生存率)。因为许多已发表的比较非肌层浸润性疾病不同治疗方法的研究随访时间较短。
1987年至1992年间纳入了261例患者,他们患有频繁复发的Ta/T1G1-G2、T1G3或原发性Tis-发育异常。患者被随机分为两组,分别接受40mg MMC或120mg BCG(丹麦1331株)治疗,每周一次,共6周,然后每月一次,持续一年,最后每三个月一次,再持续一年。通过医院档案和国家死亡原因登记册对250例可评估患者进行随访。
幸存者的中位随访时间为123个月。58例(23%)患者疾病进展,MMC组34例,BCG组24例(P = 0.26)。在140例死亡患者中,BCG组68例,MMC组72例(对数秩检验P = 0.98);大多数(95例,68%)死于其他原因。
基于对本研究患者的随访结果,无法得出最初使用的药物MMC或BCG在对疾病进展、后续治疗需求或生存率的影响方面存在差异的结论。