Midterm follow-up (3 years) confirms and extends short-term results of intravesical gemcitabine as bladder-preserving treatment for non-muscle-invasive bladder cancer after BCG failure

被引:14
|
作者
Hurle, Rodolfo [1 ]
Contieri, Roberto [1 ]
Casale, Paolo [1 ]
Morenghi, Emanuela [2 ]
Saita, Alberto [1 ]
Buffi, Nicolomaria [1 ,2 ,3 ]
Lughezzani, Giovanni [1 ,3 ]
Colombo, Piergiuseppe [4 ]
Frego, Nicola [1 ]
Fasulo, Vittorio [1 ]
Paciotti, Marco [1 ]
Guazzoni, Giorgio [1 ,3 ]
Lazzeri, Massimo [1 ]
机构
[1] Humanitas Clin & Res Ctr IRCCS, Dept Urol, Milan, Italy
[2] Humanitas Clin & Res Ctr IRCCS, Dept Med Stat, Milan, Italy
[3] Dept Biomed Sci, Dept Urol, Pieve Emanuele Milano, Italy
[4] Humanitas Clin & Res Ctr IRCCS, Dept Pathol, Milan, Italy
关键词
Bladder cancer; BCG; Gemcitabine; Intravesical therapy; BACILLUS-CALMETTE-GUERIN; CARCINOMA IN-SITU; UROTHELIAL CANCER; TRIAL; VALRUBICIN; RECURRENCE; CISPLATIN; THERAPIES; EFFICACY;
D O I
10.1016/j.urolonc.2020.09.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: There is a high demand for bladder sparing therapies in patients who do not respond to bacillus Calmette-Guerin (BCG). Objective: To report the mid-term results of intravesical gemcitabine in non-muscle-invasive bladder cancer (NMIBC) patients, who failed BCG and who were unwilling to undergo radical cystectomy (RC). Material & methods: This is an extended confirmatory open-label, single-arm study, which enrolled consecutive patients who failed BCG or were BCG intolerant and unwilling to undergo the RC (histologically confirmed Tis (CIS), T1 high grade or multifocal Ta high grade of the urinary bladder). Intravesical gemcitabine was administered once a week for 6 consecutive weeks and once a month for 12 months. The primary outcome was disease-free survival (DFS) defined as the lack of tumor on cystoscopy and negative urine cytology. The secondary endpoint was safety, defined according a grading of side effects. overall survival, progression-free survival and DFS were described with Kaplan-Meier method at 12, 24, and 36 months. Results and limitations: Overall 46 patients were enrolled. The mean follow-up was 40 months. The DFS was 69.05% at the end of induction phase and 32.69% at 36 months. The progression-free survival at 36 months was 65.38%. The overall survival and cancer specific survival were 66.97% (95% confidence interval 47.25%-80.70%) and 78.71% (95% confidence interval 59.16%-89.66%), respectively. There was no life-threatening event or treatment related death (grade 4 or 5). The most common mild and moderate adverse events reported were urinary symptoms (lower urinary tract symptoms) and fatigue (G1-G2). Conclusion: Intravesical gemcitabine seemed to represent a valid and safe alternative at 3 years follow-up for patients who failed BCG and were unwilling to undergo RC. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:195.e7 / 195.e13
页数:7
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