SALVOVAR: a pragmatic randomized phase III trial comparing the SALVage weekly dose-dense regimen to the standard 3-weekly regimen in patients with poor prognostic OVARian cancers
Year: 2025
Type: article
Study design: Study Protocol
Abstract: Background: Patients with epithelial ovarian cancer (EOC) receiving neoadjuvant platinum-based chemotherapy (NACT) who remain ineligible for complete interval cytoreductive surgery (ICS) due to poor chemosensitivity (CA-125 KELIM™ score <1.0) have a poor prognosis (~20% 5-year survival). A weekly dose-dense carboplatin-paclitaxel regimen may improve outcomes in this high-risk subgroup. Objectives: To demonstrate the superiority of a salvage weekly dose-dense carboplatin-paclitaxel regimen over continuation of the standard 3-weekly regimen in poor-prognosis EOC patients after 3-4 cycles of standard NACT. Design: SALVOVAR is a pragmatic, open-label, multicenter, international, randomized phase III trial. Methods and analysis: on days 1, 8, and 15, every 3 weeks) or the control arm (continuation of the standard regimen) for 3 cycles. Bevacizumab use is allowed at investigator discretion. Stratification factors include planned bevacizumab administration, BRCA mutation status, and KELIM strata. The two co-primary endpoints are (1) improvement in late complete cytoreduction rates (from 5% in the control arm to 20% in the experimental arm), and (2) overall survival (target hazard-ratio, 0.61). Total 250 patients will be randomized. Secondary endpoints include objective response rate, progression-free survival, and safety. Additional planned analyses include quality-of-life, cost-effectiveness, surgical standardization, human sciences, and biology studies. Ethics: The protocol was approved by the national ethics committee and health authorities. Discussion: SALVOVAR will evaluate whether chemotherapy densification improves outcomes in poorly chemosensitive advanced EOC. If positive, this pragmatic strategy could be implemented in large-scale studies, independent of resource setting. Trial registration: ClinicalTrials.gov NCT06476184 (June-2024). Available at: https://clinicaltrials.gov/study/NCT06476184.
Institutions: Hospices Civils de Lyon, Hôpital Lyon Sud, Jikei University School of Medicine, Centre Léon Bérard, European Institute of Oncology, Universitat Autònoma de Barcelona, Centro de Investigación Biomédica en Red, Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública, Institut de Recerca Sant Joan de Déu, The Christie Hospital, Institut universitaire du cancer de Toulouse Oncopole, Leiden University Medical Center, Institut Gustave Roussy, Charles University, General University Hospital in Prague, Centre Hospitalier Universitaire de Nîmes, Technion – Israel Institute of Technology, Hillel Yaffe Medical Center, Centre pour l'innovation en cancérologie de Lyon
Language: English
Subfield: Reproductive Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,800
Funder: European Commission
OpenAlex ID: W7117110232
