Anatomopathological Evaluation of a New Ultrasound-guided Transuterine Vaginal Biopsy Technique in Uterine Fibromatous Disease

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorAssistance Publique Hopitaux De Marseille

About this trial

The benign uterine fibroid is part of the broader term uterine smooth muscle tumour, which also includes malignant myometrial tumours (MSTs) of varying malignancy (uterine sarcoma, cellular fibroid, STUMP (uterine smooth muscle tumours of uncertain malignant potential)).

Magnetic resonance imaging (MRI) is the most effective test for distinguishing a fibroid from a TMM, but its reliability is limited. This leads to inappropriate management in a number of situations. The first is the risk of overtreatment by performing surgery for a suspected TMM on MRI in a patient with few or no symptoms and a final histological diagnosis of fibroid. The second is the risk of unsatisfactory or even harmful cancer surgical treatment in a symptomatic patient with a reassuring MRI diagnosis but a final histological diagnosis of TMM. Finally, there is the possibility of treating a lesion labelled as a fibroid on MRI with an alternative technique (embolisation, radiofrequency, HIFU) when it is in fact a TMM, thereby delaying appropriate treatment and worsening the prognosis.

Ultrasound-guided transuterine vaginal biopsy (ETVB) is an innovative and promising minimally invasive technique for preoperative anatomopathological diagnosis. It would make it possible to obtain a histological diagnosis without the need for surgery, thereby avoiding the inappropriate management described above.

The aim of this study is to validate an innovative minimally invasive surgical technique (BVTE) for the diagnosis of uterine smooth muscle tumours by biopsy, to assess the complications associated with the technique and any potential adverse effects, and to evaluate the feasibility of the technique in current practice.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients over 18 years of age consulting the CHU de la Conception who require surgical treatment for uterine smooth muscle tumours (fibroma or TMM).

Able to give written consent

Beneficiary or beneficiary of a social security scheme

Disqualifiers

Person in a period of exclusion from another research protocol at the time of signing consent/no objection

Pregnant women, women in labour and nursing mothers

Persons deprived of their liberty by judicial or administrative decision

Persons subject to psychiatric monitoring under articles L3112-1 and L3113-1 who are not covered by the provisions of article L1121-8

Trial design

Design model

Single group

Treatments tested in this trial

  • ultrasound-guided transuterine vaginal biopsy (BVTE)

    Other intervention

    A BVTE is performed under general anaesthetic in the operating theatre on the scheduled day of myomectomy or hysterectomy. It will be directed to the centre of the uterine smooth muscle tumour in question via an exclusively transuterine route to avoid any peritoneal spread. At least 4 to 5 samples will be taken per uterine smooth muscle tumour, with a maximum of 3 tumours to limit the risk of confusion. The woman will then be operated on as planned during the same operation. All surgical specimens will be sent to the Anatomopathology Department of La Timone for anatomopathological diagnosis after immediate formalin embedding during surgery. Surgical specimens will be analysed as usual.

Treatment groups

250 Participants
are divided into 1 treatment group
Group A: ultrasound-guided transuterine vaginal biopsy (BVTE)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Anatomopathological analysis of biopsy with BVTE technique and comparison with the reference technique

The main aim of our study will be to evaluate the diagnostic performance of a BVTE biopsy technique for preoperative uterine smooth muscle tumours to discriminate between fibroids and MCTs.

Time frame
Form enrollement to the end of the study at 43 months

Secondary outcomes

1

Number of intraoperative complications according to the Clavien-Dindo classification

The secondary objective of this study will be to count the numbre of intraoperatoire complications associated with the BVTE technique, in comparison with the reference technique.

Time frame
During the surgery
2

Number of postoperative complications according to the Clavien-Dindo classification

The secondary objective of this study will be to count the numbre of postoperatoire complications associated with the BVTE technique, in comparison with the reference technique.

Time frame
From the surgery to the end of the study at 43 months

Other outcomes

1

Number of equipment in accordance with number of patients in current practice

The exploratory objectives will be to assess the feasibility of the technique in current practice. So investigators will evaluate the number of equipment available for the technique in current practice in comparison with a reference technique.

Time frame
From enrollement to the end of the study at 43 months
2

Cost (euros) of the BVTE technique in current practice

The exploratory objectives will be to assess the feasibility of the technique in current practice. So investigators will evaluate the cost of the technique in current practice in comparison with a reference technique.

Time frame
From enrollement to the end of the study at 43 months

Sponsors and contacts

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