Collection of Endometrial Cancer-derived Organoids to Evaluate the Efficacy of PARP Inhibitors: PENDOR Pilot Study

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorCentre Francois Baclesse

About this trial

This study comprises 3 stages:

1. Collection of tumor and blood samples. 2. Creation of organoid models based on tumor samples. 3. Development of functional tests to predict clinical response to treatment.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patient aged 18 years or more

Patient with histologically confirmed, localized endometrial cancer, candidate for surgical treatment.

A high-grade endometrioid histological type and/or

P53 mutation and/or

Disqualifiers

Other active cancer less than 6 months old (with the exception of treated basal cell carcinoma of the skin).

Patient deprived of liberty, under guardianship, or subject to a legal protection measure, or unable to express consent.

Trial population

Patient with localized endometrial cancer

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • tumour and blood samples

    Other intervention

    Tumour and blood samples

Treatment groups

16 Participants
are divided into 1 treatment group
Group A: tumour and blood collection1 intervention

Trial outcomes

Primary outcomes

1

Rate of establishment of exploitable tumor organoid lines

Rate of establishment of tumor organoid lines usable for predictive assays of response to PARP inhibitors.

Time frame
through study completion, an average of 3 years

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.