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NCT Number: NCT05905315

Primary Chemoradiation VS. Neoadjuvant Chemotherapy Followed By Surgery As Treatment Strategy For LAVC

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

NKI-AVL, Amsterdam, Netherlands

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Woman ≥ 18 years
  • Signed and written informed consent.
  • Histologically-confirmed primary or recurrent squamous cell carcinoma vulvar cancer FIGO stage Ib - IVa, T1b or higher, any N, M0.
  • Local tumour through which the size or localization implies requirement of treatment through primary chemoradiation or surgery consisting of extensive surgery (meaning surgery damaging pelvic organs or exenterative surgery). This can imply;
  • T1b or larger tumour with (irresectable) groin metastases
  • T1b or larger tumour with a close relationship to and/or involvement of the urethra or anal sphincter
  • World Health Organization performance status of 0-2
  • Adequate haematological function defined by platelet count >100x10E9/L, absolute leukocyte >3X10E9/L or neutrophil count (ANC) >1.5x10E9/L, and hemoglobin >6.0 mmol/L
  • Adequate hepatic function defined by a total bilirubin level ≤1.5x the upper limit of normal (ULN) range and ASAT and ALAT levels ≤2.5x ULN for all subjects
  • Adequate renal function defined by an estimated creatinine clearance ≥50mL/min according to the Cockroft-Gault formula (or local institutional standard method)
  • Beta HCG level of 14 mIU/mL or below for women of childbearing potential
  • Highly effective contraception for patients if the risk of conception exists

Exclusion criteria

  • Patients with highly suspicious or positive metastases to the pelvic lymph nodes
  • Patients eligible for radical local excision without involvement of other organs
  • Any psychiatric condition that would prohibit the understanding or rendering of informed consent
  • Prior radiotherapy to the pelvis or groin area limiting full dose chemoradiation according to protocol
  • Existing neuropathy which will hinder the intake of chemotherapy

Treatment and study plan

Paclitaxel and Carboplatin

Drug

Paclitaxel 175 mg/m2, followed by carboplatin 5 area under the curve (AUC). This will be administered in a 3-weekly scheme.

Chemoradiation

Combination Product

According to standard treatment.

Primary outcomes

  1. Loco-regional control after 24 months per completed treatment including salvage treatment

    Time frame: 24 months after completed treatment

    Proportion of patients free from local-regional progression

Secondary outcomes

  1. Disease-related treatment failure

    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.

  2. Disease free survival

    Time frame: 24 months after completed treatment

  3. Patterns of recurrence of disease

    Time frame: 24 months after completed treatment

    Type of recurrence after treatment: local, regional or distant recurrence

  4. Overall survival

    Time frame: 24 months after completed treatment

  5. Treatment related death

    Time frame: 24 months after completed treatment

  6. Prevention of trimodal 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)

  7. Functional organ preservation

    Time frame: 24 months after completed treatment

    Proportion of patients for who an organ-sparing surgery is possible

  8. Short term and long term complications

    Time frame: 24 months after completed treatment

    According to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0

Study contacts

Contact information is provided by the study sponsor or research team.

Frederic Amant, Prof.

CONTACT

[email protected]

0031205129111

Sponsors and collaborators

Lead sponsor

The Netherlands Cancer Institute

Other

Registry information

Official study title

Primary Chemoradiation VS. Neoadjuvant Chemotherapy Followed By Surgery As Treatment Strategy For Locally Advanced Vulvar Carcinoma

Acronym: VULCANIZE-II

Important dates

Study start
2024
Primary completion
2029
Study completion
2029
First posted
Jun 15, 2023
Registry last updated
Apr 15, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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.