Paclitaxel and Carboplatin
DrugPaclitaxel 175 mg/m2, followed by carboplatin 5 area under the curve (AUC). This will be administered in a 3-weekly scheme.
NCT Number: NCT05905315
A phase 2 randomised controlled trial will be performed in which the efficacy and safety of standard treatment (primary chemoradiation; consisting of 64.5 Gy in 30 fractions of external beam radiotherapy with weekly cisplatin for six weeks) and experimental treatment (NACT; consisting of carboplatin and paclitaxel in a 3-weekly scheme) will be compared in 98 patients with LAVC, registered from eight national medical centres.
Interested in participating?
Request Info18 year and older
Female
Interventional
Phase 2
NKI-AVL, Amsterdam, Netherlands
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Paclitaxel 175 mg/m2, followed by carboplatin 5 area under the curve (AUC). This will be administered in a 3-weekly scheme.
According to standard treatment.
Time frame: 24 months after completed treatment
Proportion of patients free from local-regional progression
Time frame: 24 months after completed treatment
Patients without an event will be censored at their last date of contact. The Kaplan-Meier method will be used to estimate freedom from disease-related failure. Difference between the two main treatment arms, NACT vs. chemotherapy, will be tested using a log-rank test. Incidences of disease-related failure will be reported based on the Kaplan-Meier estimates, together with confidence intervals for the hazard ratio using both 90 and 95% confidence levels.
Time frame: 24 months after completed treatment
Time frame: 24 months after completed treatment
Type of recurrence after treatment: local, regional or distant recurrence
Time frame: 24 months after completed treatment
Time frame: 24 months after completed treatment
Time frame: 24 months after completed treatment
Proportion of patients that don't need adjuvant surgery (arm 1) and number of patients that don't need adjuvant radiotherapy (arm 2)
Time frame: 24 months after completed treatment
Proportion of patients for who an organ-sparing surgery is possible
Time frame: 24 months after completed treatment
According to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
Contact information is provided by the study sponsor or research team.
The Netherlands Cancer Institute
Other
Primary Chemoradiation VS. Neoadjuvant Chemotherapy Followed By Surgery As Treatment Strategy For Locally Advanced Vulvar Carcinoma
Acronym: VULCANIZE-II
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.