Alhogbani M Mofarej, Picard J Aude, Fassi-Fehri M Hakim, Badet J Lionel, Colombel C Marc
Department of Urology and Transplant Surgery, Hospices Civils de Lyon, Hôpital Edouard Herriot, Lyon, France.
Urol Ann. 2017 Oct-Dec;9(4):315-320. doi: 10.4103/UA.UA_115_17.
Intravesical Bacillus Calmette-Guérin (BCG) is a cause of bladder and systemic toxicity that is difficult to prevent and is responsible for treatment drop out in bladder cancer patients. More recently, BCG shortage has become the main cause of incomplete treatment.
The aim of this study was to examine the impact on long-term prognosis of bladder cancer patients following discontinuation of BCG instillations.
In this retrospective study, data were examined from 333 consecutive nonmuscle invasive bladder cancer patients treated from 2005 to 2015 by transurethral resection (TUR) and had undergone adjuvant BCG therapy after TUR.
Rate of complete cure, the reason for the interruption, toxicity, and the associations between discontinuance of BCG therapy, tumor characteristics, association with carcinoma and tumor recurrence or progression were analyzed.
Recurrence and progression-free survival rate curves were estimated using the Kaplan-Meier method and were compared using the log-rank test. Univariate and multivariate analyses were performed using the Cox proportional hazards model. Differences among groups were considered as statistically significant when < 0.05.
Overall, 303 patients were eligible for analysis. Median follow up was 36 (confidence interval: 7-120) months. A total of 55 (18.1%) had <6 installations (Group I); 87 (28.7%) completed induction and 1-year maintenance (Group III); and 161 (53.1%) completed the induction course, but not the 1-year maintenance (Group II). Grade III-IV toxicity rates were significantly higher in Group I than Group II and III. Interruption for BCG shortage was the main cause of interrupting BCG in Group II. Multivariate analysis showed that discontinuation of BCG induction therapy was an independent predictor for tumor recurrence ( < 0.001) and 1-year BCG maintenance therapy for tumor progression ( = 0.005).
Discontinuation of BCG therapy has a significantly deleterious effect on tumor recurrence and progression rates. Although BCG toxicity is a major cause of drop out, BCG shortage became a major cause of discontinuation. All effort must be done today to restore normal production of BCG worldwide.
膀胱内灌注卡介苗(BCG)会导致膀胱及全身毒性,难以预防,且是膀胱癌患者治疗中断的原因。最近,BCG短缺已成为治疗不完整的主要原因。
本研究旨在探讨停止BCG灌注后对膀胱癌患者长期预后的影响。
在这项回顾性研究中,研究人员检查了2005年至2015年间连续接受经尿道切除术(TUR)治疗且术后接受辅助BCG治疗的333例非肌层浸润性膀胱癌患者的数据。
分析完全治愈的比例、中断治疗的原因、毒性,以及BCG治疗中断、肿瘤特征、与癌的关联和肿瘤复发或进展之间的关系。
采用Kaplan-Meier法估计复发和无进展生存率曲线,并使用对数秩检验进行比较。使用Cox比例风险模型进行单因素和多因素分析。当P<0.05时,组间差异被认为具有统计学意义。
总体而言,303例患者符合分析条件。中位随访时间为36(置信区间:7-120)个月。共有55例(18.1%)接受少于6次灌注(第一组);87例(28.7%)完成诱导和1年维持治疗(第三组);161例(53.1%)完成诱导疗程,但未完成1年维持治疗(第二组)。第一组的III-IV级毒性发生率显著高于第二组和第三组。BCG短缺导致的中断是第二组中断BCG治疗的主要原因。多因素分析表明,停止BCG诱导治疗是肿瘤复发的独立预测因素(P<0.001),而1年BCG维持治疗是肿瘤进展的独立预测因素(P=0.005)。
停止BCG治疗对肿瘤复发率和进展率有显著的有害影响。虽然BCG毒性是治疗中断的主要原因,但BCG短缺已成为中断治疗的主要原因。如今必须全力以赴恢复全球BCG的正常生产。