Department of Urology, Charles Nicolle University Hospital, Rouen, France.
Clinical Investigation Center, Onco-Urology, Inserm 1404, Rouen, France.
J Clin Oncol. 2022 Jun 20;40(18):2013-2022. doi: 10.1200/JCO.21.02051. Epub 2022 Mar 7.
The optimal perioperative chemotherapy regimen for patients with nonmetastatic muscle-invasive bladder cancer is not defined.
Between February 2013 and March 2018, 500 patients were randomly assigned in 28 French centers and received either six cycles of dose-dense methotrexate, vinblastine, doxorubicin, and cisplatin (dd-MVAC) once every 2 weeks or four cycles of gemcitabine and cisplatin (GC) once every 3 weeks before surgery (neoadjuvant group) or after surgery (adjuvant group). We report the primary end point of the GETUG-AFU V05 VESPER trial (ClinicalTrials.gov identifier: NCT01812369): progression-free survival (PFS) at 3 years. Secondary end points were time to progression and overall survival.
Four hundred thirty-seven patients (88%) received neoadjuvant chemotherapy; 60% of patients received the planned six cycles in the dd-MVAC arm, 84% received four cycles in the GC arm, and thereafter, 91% and 90% of patients underwent surgery, respectively. Organ-confined response (< ypT3N0) was observed more frequently in the dd-MVAC arm (77% 63%, = .001). In the adjuvant group, 40% of patients received six cycles in the dd-MVAC arm, and 81% of patients received four cycles in the GC arm. For all patients in the clinical trial, 3-year PFS was improved in the dd-MVAC arm, but the study did not meet its primary end point (3-year rate: 64% 56%, hazard ratio [HR] = 0.77 [95% CI, 0.57 to 1.02], = .066); nevertheless, the dd-MVAC arm was associated with a significantly longer time to progression (3-year rate: 69% 58%, HR = 0.68 [95% CI, 0.50 to 0.93], = .014). In the neoadjuvant group, PFS at 3 years was significantly higher in the dd-MVAC arm (66% 56%, HR = 0.70 [95% CI, 0.51 to 0.96], = .025).
In the VESPER trial, dd-MVAC improved 3-years PFS over GC. In the neoadjuvant group, a better bladder tumor local control and a significant improvement in 3-year PFS were observed in the dd-MVAC arm.
对于非转移性肌层浸润性膀胱癌患者,最佳围手术期化疗方案尚未明确。
2013 年 2 月至 2018 年 3 月,500 例患者在 28 家法国中心被随机分配,并接受每 2 周一次的剂量密集型甲氨蝶呤、长春碱、多柔比星和顺铂(dd-MVAC)6 个周期或每 3 周一次的吉西他滨和顺铂(GC)4 个周期治疗,治疗方案为术前(新辅助组)或术后(辅助组)。我们报告了 GETUG-AFU V05 VESPER 试验的主要终点(ClinicalTrials.gov 标识符:NCT01812369):3 年无进展生存期(PFS)。次要终点为进展时间和总生存期。
437 例患者(88%)接受了新辅助化疗;dd-MVAC 组 60%的患者接受了计划的 6 个周期,GC 组 84%的患者接受了 4 个周期,此后,91%和 90%的患者分别接受了手术。dd-MVAC 组的器官局限性反应(<ypT3N0)更为常见(77% vs 63%,P=0.001)。在辅助组中,dd-MVAC 组 40%的患者接受了 6 个周期的治疗,GC 组 81%的患者接受了 4 个周期的治疗。对于临床试验中的所有患者,dd-MVAC 组的 3 年 PFS 得到改善,但该研究未达到主要终点(3 年率:64% vs 56%,风险比[HR]=0.77[95%CI,0.57 至 1.02],P=0.066);然而,dd-MVAC 组的进展时间明显延长(3 年率:69% vs 58%,HR=0.68[95%CI,0.50 至 0.93],P=0.014)。在新辅助组中,dd-MVAC 组的 3 年 PFS 显著高于 GC 组(66% vs 56%,HR=0.70[95%CI,0.51 至 0.96],P=0.025)。
在 VESPER 试验中,dd-MVAC 较 GC 改善了 3 年 PFS。在新辅助组中,dd-MVAC 组在膀胱肿瘤局部控制方面有更好的效果,并且 3 年 PFS 显著提高。