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一项多中心随机前瞻性试验,比较三种用于中危浅表性膀胱癌的膀胱内辅助治疗方法:低剂量卡介苗(27毫克)对比极低剂量卡介苗(13.5毫克)对比丝裂霉素C。

A multicentre, randomised prospective trial comparing three intravesical adjuvant therapies for intermediate-risk superficial bladder cancer: low-dose bacillus Calmette-Guerin (27 mg) versus very low-dose bacillus Calmette-Guerin (13.5 mg) versus mitomycin C.

作者信息

Ojea Antonio, Nogueira José Luís, Solsona Eduardo, Flores Nicolás, Gómez Jesús María Fernández, Molina Jesús Rodríguez, Chantada Venancio, Camacho José Emilio, Piñeiro Luís Martínez, Rodríguez Rafael Hernandez, Isorna Santiago, Blas Miguel, Martínez-Piñeiro José A, Madero Rosario

机构信息

Complejo Hospitalario Universitario de Vigo, Vigo, Spain.

出版信息

Eur Urol. 2007 Nov;52(5):1398-406. doi: 10.1016/j.eururo.2007.04.062. Epub 2007 Apr 27.

Abstract

OBJECTIVE

The primary aim was to search for lower doses of Bacillus Calmette-Guerin (BCG) that are effective and have lower toxicity.

METHODS

A low dose of BCG 27 mg was compared with BCG 13.5mg, using mitomycin C (MMC) 30 mg as the third arm of comparison. A total of 430 patients with intermediate-risk superficial bladder cancer were randomised into three groups. Instillations were repeated once a week for 6 wk followed by another six instillations given once every 2 wk during 12 wk.

RESULTS

There was a significantly longer disease-free interval for BCG 27 mg versus MMC 30 mg (p=0.006). There were no statistically significant differences between BCG 27 mg and BCG 13.5mg (p=0.165) or between BCG 13.5mg and MMC 30 mg (p=0.183). Cox proportional hazards regression showed that disease-free interval in the multivariate analysis was significantly better for primary disease and treatment with BCG 27 mg. There were no significant differences among the three groups with regards to time to progression and cancer-specific survival time. Local and systemic toxicity were higher in both BCG treatment groups.

CONCLUSIONS

One third of the standard dose, BCG 27 mg, seems to be the minimum effective dose as adjuvant treatment for intermediate-risk superficial bladder cancer, being more effective than MMC 30 mg. One sixth of the standard dose, BCG 13.5mg, has the same efficacy as MMC 30 mg but it is more toxic.

摘要

目的

主要目的是寻找有效且毒性较低的卡介苗(BCG)低剂量。

方法

将低剂量的27毫克BCG与13.5毫克BCG进行比较,以30毫克丝裂霉素C(MMC)作为第三组对照。总共430例中危浅表性膀胱癌患者被随机分为三组。每周重复灌注一次,共6周,随后在12周内每2周再进行6次灌注。

结果

27毫克BCG组的无病间期明显长于30毫克MMC组(p = 0.006)。27毫克BCG组与13.5毫克BCG组之间(p = 0.165)或13.5毫克BCG组与30毫克MMC组之间(p = 0.183)无统计学显著差异。Cox比例风险回归显示,在多变量分析中,原发性疾病和27毫克BCG治疗的无病间期明显更好。三组在进展时间和癌症特异性生存时间方面无显著差异。两个BCG治疗组的局部和全身毒性均较高。

结论

标准剂量的三分之一,即27毫克BCG,似乎是中危浅表性膀胱癌辅助治疗的最低有效剂量,比30毫克MMC更有效。标准剂量的六分之一,即13.5毫克BCG,与30毫克MMC具有相同的疗效,但毒性更大。

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