The Absolute Effect / Evidence / VESPER (GETUG-AFU V05 / COGB 0402)
Bladder Cancer · Medical Oncology · Neoadjuvant

VESPER (GETUG-AFU V05 / COGB 0402)

Clinical question

Which cisplatin-based neoadjuvant regimen is preferable before cystectomy: ddMVAC or gemcitabine-cisplatin?

Trial context
Population
493 patients with localized muscle-invasive bladder cancer eligible for cisplatin-based neoadjuvant chemotherapy
Intervention
Dose-dense MVAC vs gemcitabine-cisplatin before cystectomy
Key endpoint
5-year overall survival
Time horizon / follow-up
Long-term follow-up
Absolute Effect

What changes for patients?

VESPER established that dose-dense MVAC is a reasonable intensive neoadjuvant regimen, with higher pathologic response and favorable event-free outcomes compared with gemcitabine-cisplatin. Five-year OS was about 71% vs 66%, an absolute difference of 5 points (NNT 20), but the principal value of the trial is regimen selection rather than a large OS effect. NNT is based on 5-year OS.

NNT: 20

Treatment burden / harm

Grade 3–5 toxicity

NNH: Not quantified here; ddMVAC has a different toxicity profile and requires growth-factor support

Relative effect

HR: 0.77 for event-free survival in bladder/lymph-node population; OS difference modest

Trial primarily demonstrated regimen differences in downstaging and event-free outcomes

Clinical interpretation

VESPER supports dose-dense MVAC as a perioperative option for fit MIBC patients, particularly in the neoadjuvant setting, with treatment delivery and toxicity affecting the choice.

Primary publication

← Return to The Absolute Effect

Current-practice context · reviewed 14 October 2026

VESPER supports dose-dense MVAC as a perioperative option for fit patients with muscle-invasive bladder cancer, with improved progression-related outcomes compared with gemcitabine–cisplatin in the neoadjuvant subgroup and important toxicity/treatment-delivery considerations. Regimen choice should reflect renal function, fitness, tumour stage, local expertise and current perioperative immunotherapy options; do not equate the trial with a universal superiority claim across every perioperative setting.

VESPER primary report ↗ · Current guideline guidance ↗