Recent developments in perioperative combination therapy in muscle-invasive bladder cancer

被引:3
|
作者
Mellema, Jan-Jaap J. [1 ,2 ]
van Rhijn, Bas W. G. [3 ]
van der Heijden, Michiel S. [1 ,2 ]
机构
[1] Netherlands Canc Inst, Dept Med Oncol, Amsterdam, Netherlands
[2] Netherlands Canc Inst, Dept Surg Oncol Urol, Amsterdam, Netherlands
[3] Univ Regensburg, Caritas St Josef Med Ctr, Dept Urol, Regensburg, Germany
关键词
chemotherapy; combination therapy; immunotherapy; muscle-invasive bladder cancer; perioperative treatment; urothelial carcinoma; UROTHELIAL CARCINOMA; NEOADJUVANT CHEMOTHERAPY; OPEN-LABEL; PHASE-II; PEMBROLIZUMAB; NIVOLUMAB; ADJUVANT; ATEZOLIZUMAB; MULTICENTER; CYSTECTOMY;
D O I
10.1097/MOU.0000000000001107
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 of review A summary of recent literature to provide a comprehensive overview of the current state of systemic perioperative treatment combinations for muscle-invasive bladder cancer (MIBC). Recent findings We discuss recent developments in standard and experimental treatment modalities. The VESPER trial has shown that six cycles of neoadjuvant dose-dense MVAC are superior to four cycles of gemcitabine/cisplatin (GC), though it is unclear whether the superiority is derived from the specific regimen or number of cycles. Adjuvant cisplatin-based chemotherapy, a subject of longstanding debate, was shown to have comparable overall survival-benefit to neoadjuvant chemotherapy in an updated meta-analysis. Neoadjuvant chemotherapy and anti-PD-(L)1 show encouraging results, but with no comparative studies to standard care, context is lacking. Immunotherapeutic neoadjuvant anti-CTLA-4/PD-(L)1 combinations or combinations of checkpoint inhibitors with antibody-drug-conjugates are in early stages of development and show promising preliminary results. Summary Six cycles of neoadjuvant dose-dense MVAC are superior to four cycles of gemcitabine/cisplatin. Adjuvant cisplatin-based chemotherapy is a viable option for patients with high-risk tumours who did not receive prior neoadjuvant treatment. The added value of anti-PD-(L)1 to chemotherapy still needs to be established. Novel developments in immunotherapy combinations, while promising, are still in an early stage and randomized studies are ongoing.
引用
收藏
页码:404 / 411
页数:8
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