Marcq Gautier, Jarry Edouard, Ouzaid Idir, Hermieu Jean-François, Henon François, Fantoni Jean-Christophe, Xylinas Evanguelos
CHU Lille, Urology department, Rue Michel Polonovski, Hôpital Claude Huriez, F-59000, Lille, France.
Urology department, Hôpital Claude Huriez, Lille, France.
Ther Adv Urol. 2019 Jan 28;11:1756287218823678. doi: 10.1177/1756287218823678. eCollection 2019 Jan-Dec.
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).
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.
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.
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.
我们旨在对使用新辅助化疗(NAC)的非转移性肌层浸润性膀胱癌(MIBC)患者的最佳实践管理进行全面的文献综述。
2018年7月至9月期间,我们使用MEDLINE和EMBASE电子文献数据库进行了系统综述。检索策略包括以下术语:新辅助治疗和膀胱肿瘤。
单药铂类化疗没有益处。铂类新辅助化疗是金标准治疗,主要由顺铂、长春碱、甲氨蝶呤、多柔比星、吉西他滨甚至表柔比星(MVAC)联合组成。5年时,MVAC的绝对总生存获益为5%,无病生存率绝对提高了9%。观察到这种效果与局部治疗类型无关,且在患者亚组之间没有差异。此外,根治性膀胱切除术后的ypT0期(完全病理缓解)是改善肿瘤学结局的替代标志物。高密度MVAC已被证明可降低毒性(3-4级毒性范围为0%至26%),而不影响肿瘤学结局。迄今为止,对于不适合基于顺铂的新辅助化疗的患者,在新辅助治疗中使用卡铂没有作用。到目前为止,尚无已发表的试验评估免疫疗法在新辅助治疗中的作用,但许多有前景的研究正在进行中。
有强有力的证据支持在新辅助治疗中临床使用高剂量强度的甲氨蝶呤、长春碱、多柔比星和顺铂联合方案。随着新兴免疫疗法的出现,MIBC治疗格局在不久的将来应该会有所发展。