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密集型甲氨蝶呤、长春碱、多柔比星、顺铂或吉西他滨和顺铂作为非转移性肌层浸润性膀胱癌患者的围手术期化疗:GETUG-AFU V05 VESPER 试验的结果。

Dose-Dense Methotrexate, Vinblastine, Doxorubicin, and Cisplatin or Gemcitabine and Cisplatin as Perioperative Chemotherapy for Patients With Nonmetastatic Muscle-Invasive Bladder Cancer: Results of the GETUG-AFU V05 VESPER Trial.

机构信息

Department of Urology, Charles Nicolle University Hospital, Rouen, France.

Clinical Investigation Center, Onco-Urology, Inserm 1404, Rouen, France.

出版信息

J Clin Oncol. 2022 Jun 20;40(18):2013-2022. doi: 10.1200/JCO.21.02051. Epub 2022 Mar 7.

Abstract

PURPOSE

The optimal perioperative chemotherapy regimen for patients with nonmetastatic muscle-invasive bladder cancer is not defined.

PATIENTS AND METHODS

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.

RESULTS

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).

CONCLUSION

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.

摘要

目的

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。

方法

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。

结果

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)。

结论

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。

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