Contemporary best practice in the use of neoadjuvant chemotherapy in muscle-invasive bladder cancer

被引:17
作者
Marcq, Gautier [1 ]
Jarry, Edouard [2 ]
Ouzaid, Idir [3 ]
Hermieu, Jean-Francois [2 ,3 ]
Henon, Francois [2 ]
Fantoni, Jean-Christophe [2 ]
Xylinas, Evanguelos [3 ]
机构
[1] CHU Lille, Urol Dept, Hop Claude Huriez, Rue Michel Polonovski, F-59000 Lille, France
[2] Hop Claude Huriez, Urol Dept, Lille, France
[3] Paris Descartes Univ, Dept Urol, Paris, France
关键词
immunotherapy; muscle-invasive bladder cancer; neoadjuvant chemotherapy (NAC); platinum-based chemotherapy; TRANSITIONAL-CELL-CARCINOMA; GEMCITABINE PLUS CISPLATIN; METASTATIC UROTHELIAL CARCINOMA; RADICAL CYSTECTOMY; ACCELERATED METHOTREXATE; M-VAC; DOXORUBICIN; VINBLASTINE; SURVIVAL; THERAPY;
D O I
10.1177/1756287218823678
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
Background: We aimed to provide a comprehensive literature review on the best practice management of patients with nonmetastatic muscle-invasive bladder cancer (MIBC) using neoadjuvant chemotherapy (NAC). Method: Between July and September 2018, we conducted a systematic review using MEDLINE and EMBASE electronic bibliographic databases. The search strategy included the following terms: Neoadjuvant Therapy and Urinary Bladder Neoplasms. Results: There is no benefit of a single-agent platinum-based chemotherapy. Platinum-based NAC is the gold standard therapy and mainly consists of a combination of cisplatin, vinblastine, methotrexate, doxorubicin, gemcitabine or even epirubicin (MVAC). At 5 years, the absolute overall survival benefit of MVAC was 5% and the absolute disease-free survival was improved by 9%. This effect was observed independently of the type of local treatment and did not vary between subgroups of patients. Moreover, a ypT0 stage (complete pathological response) after radical cystectomy was a surrogate marker for improved oncological outcomes. High-density MVAC has been shown to decrease toxicity (with a grade 3-4 toxicity ranging from 0% to 26%) without impacting oncological outcomes. To date, there is no role for carboplatin administration in the neoadjuvant setting in patients that are unfit for cisplatin-based NAC administration. So far, there is no published trial evaluating the role of immunotherapy in a neoadjuvant setting, but many promising studies are ongoing. Conclusion: There is a strong level of evidence supporting the clinical use of a high-dose-intensity combination of methotrexate, vinblastine, doxorubicin and cisplatin in a neoadjuvant setting. The landscape of MIBC therapies should evolve in the near future with emerging immunotherapies.
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页码:1 / 8
页数:8
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