首页> 外文期刊>The Journal of Urology >Intravesical gemcitabine for high risk, nonmuscle invasive bladder cancer after bacillus Calmette-Guérin treatment failure
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Intravesical gemcitabine for high risk, nonmuscle invasive bladder cancer after bacillus Calmette-Guérin treatment failure

机译:卡介苗治疗失败后,膀胱内吉西他滨治疗高危,非肌肉浸润性膀胱癌

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Purpose: We report our experience with intravesical gemcitabine for bladder cancer after failed bacillus Calmette-Guérin treatment. Materials and Methods: We retrospectively reviewed the records of patients at our cancer center treated with intravesical gemcitabine after bacillus Calmette- Guérin failure. We estimated progression-free, recurrence-free and cancer specific survival using the cumulative incidence function, considering death from another cause as a competing risk. Comparisons were made using the Gray test. Overall survival was estimated using the Kaplan-Meier method and differences were compared with the log rank test. Results: Of 69 patients treated with intravesical gemcitabine 37 had bacillus Calmette-Guérin refractory disease. Median followup in progression-free patients was 3.3 years. Progression-free and cancer specific survival were similar in patients with refractory disease and those with other types of bacillus Calmette- Guérin failure. Overall survival was lower in patients with refractory disease (58% vs 71%) but this was not statistically significant (p = 0.096). Of the patients 27 patients experienced a complete response. Progression-free, cancer specific and overall survival did not differ significantly between patients with and without a complete response. Cystectomy was subsequently performed in 20 patients. Those with a complete response had a delayed time to cystectomy and no muscle invasive bladder cancer at cystectomy. There were no serious adverse events and only a minority of patients discontinued treatment due to adverse events. Conclusions: In our experience intravesical gemcitabine should be considered after bacillus Calmette-Guérin failure in patients with bladder cancer who refuse radical cystectomy or who are not candidates for major surgery.
机译:目的:我们报告在卡介苗治疗后失败的膀胱内吉西他滨治疗膀胱癌的经验。材料和方法:我们回顾性研究了卡介苗失败后,在我们癌症中心接受膀胱内吉西他滨治疗的患者的记录。我们使用累积发病率函数估算了无进展,无复发和癌症特异性生存率,并将其他原因的死亡视为竞争风险。使用灰色检验进行比较。使用Kaplan-Meier方法估算总体生存率,并将差异与对数秩检验进行比较。结果:在接受膀胱内吉西他滨治疗的69例患者中,37例患有卡介苗-卡林芽孢杆菌顽固性疾病。无进展患者的中位随访时间为3。3年。难治性疾病患者和其他类型的卡介苗-卡伦杆菌衰竭患者的无进展生存期和癌症特异性生存率相似。难治性疾病患者的总生存率较低(分别为58%和71%),但无统计学意义(p = 0.096)。在这些患者中,有27位患者完全缓解。有无完全缓解的患者之间无进展,癌症特异性和总体生存率无显着差异。随后在20例患者中进行了膀胱切除术。反应完全的患者膀胱切除术时间延迟,并且在膀胱切除术中无肌肉浸润性膀胱癌。没有严重的不良事件,只有少数患者因不良事件而中止治疗。结论:根据我们的经验,对于拒绝进行根治性膀胱切除术或不适合进行大手术的膀胱癌患者,在卡介苗-卡林杆菌失败后应考虑使用吉西他滨。

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