NODE (groiN ultrasOunD cancEr)
This study is an open label, prospective, experimental, randomised clinical trial. The primary aim of this study is to determine whether it is feasible to randomise vulvar cancer patients into one of two treatment arms:1) surgical groin node dissection (as delivered though either a sentinel node biopsy or inguinofemoral lymph node dissection (IFL), or 2) serial high-resolution bilateral groin ultrasound surveillance and clinical examination every 2 months.
Study details:
Treatment of vulvar cancer causes significant morbidity. Despite being a rare cancer, at least 2500 survivors of vulvar cancer live in Australia. Most survivors live with the detrimental, life-long impacts resulting from their cancer treatment because there are currently no alternatives to mitigate these impacts.
The personal and societal burden this entails is significant. To control such cancer-associated burden is a national priority. Clinical palpation of the groin region and computed tomography (CT) scans do not reliably detect groin node involvement.
Hence, current clinical guidelines recommend all women diagnosed at apparent Stage I or II have a surgical groin LND. This can be performed as a full IFL (full LND) to remove all groin nodes, or as a SNB to remove selected (one or two) nodes. SNB is less invasive, however, is appropriate only for vulvar cancers \<4cm in diameter and unifocal tumours (\~50% of all Stage I and II vulvar cancers).
SNB is also associated with a false negative rate (10%) that increases the risk of undetected nodes. In 25% of cases (\~80 Australian women per year), groin LND will reveal positive nodes (i. e.
, metastases), which triggers a referral for radiation treatment. If positive groin nodes are missed, and over time become enlarged, clinically palpable and attached to the overlying skin, \>90% of women will die within 12 months, despite subsequent treatment. Conversely, if groin node involvement is detected early (e.
g. , by ultrasound) while still small, survival outcomes are excellent. Ultrasound technology is potentially as accurate as LND due to recent advances in resolution and technologies such as 2D/3D volumetric assessments and tissue flow.
Furthermore, ultrasound is superior to medical resonance imaging (MRI), and to standard CT and positron emission tomography (PET) scans in capturing groin node involvement because it has a higher resolution, avoids harmful radiation and the technology is readily accessible outside of high-volume metropolitan areas. The investigators propose to reduce surgical morbidity by replacing upfront groin LND for vulvar cancer patients with serial high-resolution ultrasound to detect groin metastases. Groin LND will only be necessary for the few women with ultrasound-detected metastases when they are still small.
This feasibility study (NODE - groiN ultrasOunD cancer) will determine the value of randomized serial groin ultrasound examinations in stage I and II vulvar cancer patients and whether it is feasible and safe for the investigators to de-escalate the extent of vulvar cancer surgery, aiming to achieve improved outcomes for affected patients. Australian women with this rare cancer bear an unacceptably high (and potentially avoidable) treatment-related burden. This feasibility study is the first step to address this problem in a novel yet pragmatic way.
The overall outcome of NODE is a novel, less invasive alternative to vulvar cancer LND associated with significantly less morbidity, without compromising survival.
Eligibility criteria
Researchers look for people who fit a certain description, called eligibility criteria. See if you qualify.
Inclusion criteria
- Women, over 18 years, with histologically confirmed SCC, adenocarcinoma or melanoma of the vulva
- Clinically stage I or II on medical imaging (CT scan of pelvis, abdomen, and chest), without evidence of regional or distant metastatic disease
- Participant must be suitable to undergo IFL/SNB according to local clinical practice management guidelines
- Signed written informed consent
- Negative serum pregnancy test ≤ 30 days of surgery in pre-menopausal women and women < 2 years after the onset of menopause
- Patient lives within 40 km of a medical diagnostic imaging centre (site investigator approval required for special circumstances)
Exclusion criteria
- Women with non-invasive vulvar conditions (e.g. non-invasive non-mammary Paget's disease)
- Squamous cell carcinoma (SCC) of the vulva with depth of invasion ≤1 mm
- Clinical or medical imaging evidence of regional and/or distant metastatic disease
- Serious concomitant systemic disorders incompatible with the study (at the discretion of the investigator)
- Other prior malignancies <5 years before inclusion, except for successfully treated keratinocyte skin cancers, or ductal carcinoma in situ
- Estimated life expectancy of ≤6 months
Eligibility
Age eligible for study : NA
Healthy volunteers accepted : No
Gender eligible for study: FEMALE
Things to know
Study dates
Study start:
Primary completion:
Study completion finish:
Study type
OTHER
Phase
- NA
Study ID
NCT06264167
Intervention or treatment
DIAGNOSTIC_TEST: High-resolution bilateral groin ultrasound surveillance
Conditions
- Vulvar Cancer Stage Ib
- Vulvar Cancer Stage II
- Lymph Node Metastasis
- Groin Node
- Ultrasound Therapy; Complications
You may be eligible to participate in this trial based on your search. Check eligibility by answering some questions.
Research sites nearby
Closest Location:
St Andrew's War Memorial Hospital
Select from list below to view details:
St Andrew's War Memorial Hospital
Brisbane, Queensland, Australia
Royal Brisbane and Women's Hospital
Brisbane, Queensland, Australia
Buderim Private Hospital
Sunshine Coast, Queensland, Australia
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Who is running the clinical trial?
Queensland Centre for Gynaecological Cancer
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
| Participant Group/Arm | Intervention/Treatment |
|---|---|
EXPERIMENTAL: Participants with normal/negative baseline groin ultrasounds
| Diagnostic Test: High-resolution bilateral groin ultrasound surveillance |
NO_INTERVENTION: Participants with normal/negative baseline groin ultrasounds - Standard Care
| |
NO_INTERVENTION: Participants with suspicious/indeterminate baseline groin ultrasound
|
What is the study measuring?
Primary Outcome
| Measure | Description | Time Frame |
|---|---|---|
| Feasibility of randomisation: The percentage of patients willing to be randomised to either surgical groin node dissection or serial high-resolution bilateral groin ultrasound surveillance in conjunction with clinical examination every 2 months. | The feasibility of randomisation into (1) LND (IFL vs SNB) or (2) high-resolution bilateral groin ultrasound surveillance every 2 months will be determined through a practical sample size of n=20. Feasibility is declared if 30% of eligible patients (n=6 or more) can be randomised. | 12 months |
Secondary Outcome
| Measure | Description | Time Frame |
|---|---|---|
| Utility of tumour mutations to determine positive lymph node metastasis. | Translational research - Compare the molecular profile of tumour mutations between positive and negative lymph nodes. | Study duration up to 15 years |
| Utility of circulating tumour DNA to determine positive lymph node metastasis. | Translational research - Compare the molecular profile of circulating tumour DNA between positive and negative lymph nodes. | Study duration up to 15 years |
| Utility of plasma to determine positive lymph node metastasis. | Translational research - Compare the molecular profile of plasma between positive and negative lymph nodes. | Study duration up to 15 years |
| Utility of serum to determine positive lymph node metastasis. | Translational research - Compare the molecular profile of serum between positive and negative lymph nodes. | Study duration up to 15 years |
References
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