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

Author:

Pfister Christian12ORCID,Gravis Gwenaelle3ORCID,Fléchon Aude4,Chevreau Christine5,Mahammedi Hakim6,Laguerre Brigitte7,Guillot Aline8,Joly Florence9ORCID,Soulié Michel10,Allory Yves11ORCID,Harter Valentin12ORCID,Culine Stéphane13ORCID,

Affiliation:

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

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

3. Department of Medical Oncology, Paoli-Calmette Institute, Marseille, France

4. Department of Medical Oncology, Léon Bérard Cancer Center, Lyon, France

5. Department of Medical Oncology, ICR-IUCT Oncopole, Toulouse, France

6. Department of Medical Oncology, Jean Perrin Cancer Center, Clermont-Ferrand, France

7. Department of Medical Oncology, Eugène Marquis Cancer Center, Rennes, France

8. Department of Medical Oncology, Lucien Neuwirth Cancer Institute, St Priest, France

9. Department of Medical Oncology, Baclesse Cancer Center, Caen, France

10. Department of Urology, Rangueil University Hospital, Toulouse, France

11. Department of Pathology, Curie Institute, Saint-Cloud, France

12. North-West Canceropole Data Center, Baclesse Cancer Center, Caen, France

13. Department of Medical Oncology, Saint-Louis Hospital, AP-HP, Faculté de Paris, France

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% v 63%, P = .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% v 56%, hazard ratio [HR] = 0.77 [95% CI, 0.57 to 1.02], P = .066); nevertheless, the dd-MVAC arm was associated with a significantly longer time to progression (3-year rate: 69% v 58%, HR = 0.68 [95% CI, 0.50 to 0.93], P = .014). In the neoadjuvant group, PFS at 3 years was significantly higher in the dd-MVAC arm (66% v 56%, HR = 0.70 [95% CI, 0.51 to 0.96], P = .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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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