STRatIfication of Vulvar Squamous Cell Carcinoma by HPV and p53 Status to Guide Excision

ConditionVulvar Cancer
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorBritish Columbia Cancer Agency

About this trial

Vulvar cancer affects the external genitalia of women. This type of cancer is uncommon, arising mostly in older women and has been neglected in research and clinical trials. Over the recent years, investigators have learned that the most common type of vulvar cancer; vulvar squamous cell carcinoma (VSCC) develops from pre-cancerous lesions via different pathways. One pathway is associated with human papillomavirus (HPV) infection, and another is related to chronic inflammatory skin conditions (and not HPV). The VSCCs arising from these two principal pathways; HPV- associated (HPV A) and HPV-independent (HPV I), behave differently with different risks of recurrence, and different response to treatments. HPV-I VSCC are further defined by mutations in TP53 (Tumor Protein 53), which identify a group of patients with aggressive disease. Currently treatment is the same for all women with vulvar cancer, and consequently many women may be overtreated, and many women are not treated enough. Given evolving knowledge of this disease, this 'one size fits all' approach may no longer be appropriate. The investigators aim in this study is to see if personalizing surgical therapy for patients with vulvar cancer based on HPV and TP53 status will improve outcomes.

Eligibility criteria

Qualifiers

Histologically confirmed primary diagnosis of vulvar squamous cell carcinoma

Surgically staged FIGO (International Federation of Gynaecology and Obstetrics) I-II disease

HPV-I VSCC: margins are negative for cancer but <8mm, and/or positive for dVIN, and/or positive for p53 abnormality on IHC

HPV-A VSCC: margins are negative for cancer but <8mm (regardless of in-situ (HSIL) margin status)

Disqualifiers

Recurrent vulvar squamous cell carcinoma

Non-squamous cell carcinoma histotypes

FIGO stage III- IV disease

Patients referred for adjuvant radiation for close margins

Trial design

Treatments tested in this trial

  • Re-excision

Treatment groups

249 Participants
are divided into 2 treatment groups

Sponsors and collaborators

British Columbia Cancer Agency

Lead sponsor

Gynecologic Cancer Initiative

Collaborator

Australia New Zealand Gynaecological Oncology Group

Collaborator

Canadian Cancer Trials Group

Collaborator