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首页> 外文期刊>Arab Journal of Urology >A comparative study between full-dose and half-dose intravesical immune bacille Calmette–Guérin injection in the management of superficial bladder cancer
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A comparative study between full-dose and half-dose intravesical immune bacille Calmette–Guérin injection in the management of superficial bladder cancer

机译:膀胱浅表癌全剂量和半剂量腔内免疫杆菌卡介苗注射液的比较研究

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Objectives To determine whether a half-dose of bacille Calmette–Guérin (BCG) can reduce toxicity without affecting its efficacy in the management of non-muscle-invasive bladder cancer. Patients and methods From January 2012 to January 2014, 80 patients with superficial bladder cancer and in the intermediate-risk group were simply randomised to receive two different doses of BCG, i.e., a full dose of 90 mg (group A) or a half-dose of 45 mg (group B). There were no significant differences in clinical and pathological characteristics between the groups. At completion of the study, 40 patients could be evaluated in each group. Results All patients were evaluated for a follow-up of 12 months after treatment. There was no significant difference in recurrence rate (15 patients, 38%, in group A and 16, 40%, in group B) in the two groups, and no difference in progression rate of the disease, at eight patients (20%) in each group. There were significant differences between groups A and B in toxicity (grade 1 adverse events, 70% vs. 60%; grade 2, 18% vs. 7.5%, respectively). Grade 3 adverse events were only reported in group A (2.5%). Conclusion The half dose of intravesical BCG instillation can reduce the toxicity and side-effects that are associated with the treatment of superficial bladder cancer, without affecting the efficacy of therapy.
机译:目的确定半剂量的卡介苗(BCG)能否降低毒性而不影响其在非肌肉浸润性膀胱癌治疗中的功效。患者和方法从2012年1月至2014年1月,将80例浅表性膀胱癌和中危组的患者随机分为两组,分别接受两种剂量的BCG,即全剂量90 mg(A组)或半剂量。剂量为45毫克(B组)。两组之间的临床和病理特征无显着差异。在研究完成时,每组可评估40名患者。结果所有患者均接受治疗后12个月的随访评估。两组的复发率无显着性差异(A组为15例,38%,B组为16,40%,8例(20%),疾病进展率无差异在每个组中。 A组和B组在毒性方面有显着差异(1级不良事件分别为70%和60%; 2级不良事件分别为18%和7.5%)。仅在A组中报告了3级不良事件(2.5%)。结论膀胱内BCG滴注半剂量可减少与治疗浅表性膀胱癌相关的毒性和副作用,而不影响治疗效果。

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