Department of Urology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
Division of Biostatistics, Department of Radiation Oncology, Massachusetts General Hospital, Boston, Massachusetts.
J Urol. 2018 Feb;199(2):407-415. doi: 10.1016/j.juro.2017.08.106. Epub 2017 Sep 1.
We describe the incidence, clinicopathological risk factors, management and outcomes of recurrent nonmuscle invasive bladder cancer after a complete response to trimodality therapy of muscle invasive bladder cancer.
We retrospectively reviewed the records of 342 patients with cT2-4aN0M0 muscle invasive bladder cancer and a complete response after trimodality therapy from 1986 to 2013. Using competing risks analyses we examined the association between baseline clinicopathological variables and nonmuscle invasive bladder cancer outcomes. Kaplan-Meier and the generalized Fleming-Harrington test were used to compare disease specific and overall survival.
At a median followup of 9 years nonmuscle invasive bladder cancer recurred in 85 patients (25%) who had had a complete response. On Kaplan-Meier analysis baseline carcinoma in situ was associated with recurrent nonmuscle invasive bladder cancer (p = 0.02). However, on multivariate analysis carcinoma in situ and other baseline clinicopathological characteristics did not predict such recurrence. Patients with recurrent nonmuscle invasive bladder cancer had worse 10-year disease specific survival than those without recurrence (72.1% vs 78.4%, p = 0.002), although overall survival was similar (p = 0.66). Of the 39 patients (46%) who received adjuvant intravesical bacillus Calmette-Guérin 29 (74%) completed induction therapy and 19 (49%) reported bacillus Calmette-Guérin toxicity. Three-year recurrence-free and progression-free survival after induction bacillus Calmette-Guérin was 59% and 63%, respectively.
After a complete response to trimodality therapy nonmuscle invasive bladder cancer recurred in 25% of patients, developing in some of them more than a decade after trimodality therapy. No baseline clinicopathological characteristics were associated with such recurrence after a complete response. Patients with nonmuscle invasive bladder cancer recurrence had worse disease specific survival than those without such recurrence but similar overall survival. Adjuvant intravesical bacillus Calmette-Guérin had a reasonable toxicity profile and efficacy in this population. Properly selected patients with recurrent nonmuscle invasive bladder cancer after a complete response may avoid immediate salvage cystectomy.
我们描述了完全缓解肌层浸润性膀胱癌三联疗法后非肌层浸润性膀胱癌复发的发生率、临床病理危险因素、处理方法和结果。
我们回顾性分析了 1986 年至 2013 年间 342 例接受过三联疗法治疗且完全缓解的 cT2-4aN0M0 肌层浸润性膀胱癌患者的记录。我们使用竞争风险分析检查了基线临床病理变量与非肌层浸润性膀胱癌结局之间的关系。Kaplan-Meier 法和广义 Fleming-Harrington 检验用于比较疾病特异性和总体生存率。
在中位随访 9 年后,85 例(25%)完全缓解的患者发生非肌层浸润性膀胱癌复发。在 Kaplan-Meier 分析中,基线原位癌与非肌层浸润性膀胱癌复发相关(p = 0.02)。然而,在多变量分析中,原位癌和其他基线临床病理特征并不能预测这种复发。复发非肌层浸润性膀胱癌患者的 10 年疾病特异性生存率低于未复发患者(72.1% vs 78.4%,p = 0.002),尽管总体生存率相似(p = 0.66)。在 39 例(46%)接受辅助膀胱内卡介苗治疗的患者中,29 例(74%)完成了诱导治疗,19 例(49%)报告了卡介苗毒性。诱导卡介苗治疗后 3 年无复发和无进展生存率分别为 59%和 63%。
在完全缓解三联疗法后,25%的患者发生非肌层浸润性膀胱癌复发,其中一些患者在三联疗法后 10 多年才复发。完全缓解后,没有基线临床病理特征与这种复发相关。发生非肌层浸润性膀胱癌复发的患者疾病特异性生存率比未发生这种复发的患者差,但总体生存率相似。辅助膀胱内卡介苗治疗在该人群中具有合理的毒性谱和疗效。适当选择完全缓解后复发的非肌层浸润性膀胱癌患者可能避免立即进行挽救性膀胱切除术。