Intravesical gemcitabine for non-muscle invasive bladder cancer: An abridged Cochrane Review

被引:9
|
作者
Han, Mi Ah [1 ]
Maisch, Philipp [2 ]
Jung, Jae Hung [3 ,4 ]
Hwang, Jun Eul [5 ]
Narayan, Vikram [6 ]
Cleves, Anne [7 ]
Hwang, Eu Chang [8 ]
Dahm, Philipp [9 ,10 ]
机构
[1] Chosun Univ, Dept Prevent Med, Coll Med, Gwangju, South Korea
[2] Tech Univ Munich, Dept Urol, Rechtsder Isar Med Ctr, Munich, Germany
[3] Yonsei Univ, Dept Urol, Wonju Coll Med, Wonju, South Korea
[4] Yonsei Univ, Inst Convergence Sci, Ctr Evidence Based Med, Seoul, South Korea
[5] Chonnam Natl Univ, Dept Hematol Oncol, Sch Med, Gwangju, South Korea
[6] Emory Univ, Dept Urol, Atlanta, GA USA
[7] Cardiff Univ, Velindre NHS Trust, Lib Serv, Cardiff, Wales
[8] Chonnam Natl Univ, Dept Urol, Sch Med, Gwangju, South Korea
[9] Minneapolis VA Hlth Care Syst, Urol Sect, Minneapolis, MN USA
[10] Univ Minnesota, Dept Urol, Minneapolis, MN USA
关键词
Administration; intravesical; Gemcitabine; Systematic review; Urinary bladder neoplasms; BACILLUS-CALMETTE-GUERIN; EFFICACY; THERAPY; QUALITY; CLASSIFICATION; INSTILLATION; CARCINOMA;
D O I
10.4111/icu.20210265
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: To assess the comparative effectiveness and toxicity of intravesical gemcitabine instillation for non-muscle invasive bladder cancer (NMIBC). Materials and Methods: We performed a comprehensive literature search on 11 September 2020. We included RCTs in which participants received intravesical gemcitabine for primary or recurrent NMIBC. Two review authors independently assessed the included studies and extracted data for the primary outcomes (time to recurrence, time to progression, grade III to V adverse events) and the secondary outcomes (time to death from bladder cancer, time to death from any cause, grade I or II adverse events, and disease-specific quality of life). We performed statistical analyses using a random-effects model and rated the certainty of the evidence using GRADE. Results: We found seven studies with 1,222 participants. Gemcitabine may reduce the risk of recurrence over time, but may have a similar effect on progression and grade III to V adverse events compared to saline. Gemcitabine may reduce recurrence and progression compared to mitomycin. We are uncertain about the effect of gemcitabine on the grade III to V adverse events compared to mitomycin. Gemcitabine may reduce recurrence and progression compared to giving BCG again in recurrent high-risk NMIBC after BCG treatment. Conclusions: Based on the findings of this review, gemcitabine may have a favorable impact on recurrence and progression-free survival than saline and mitomycin but we are uncertain about how major adverse events compare. The same is true when comparing gemcitabine to BCG in individuals with high-risk diseases who have previously failed BCG.
引用
收藏
页码:623 / 630
页数:8
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