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Taking people in FrancePhase 2

Tests durvalumab with chemotherapy before surgery in upper urinary tract cancer

Tests durvalumab with chemotherapy before surgery in adults with urothelial cancer.

Key facts

Who runs it
Centre Hospitalier Universitaire De Nimes
Where
Nîmes, FranceSee the site
Registry title
Safety and Efficacy of Neoadjuvant immunotherapy with Durvalumab (MEDI 4736) in combination with neoadjuvant chemotherapy (Gemcitabin/Cisplatin or Gemcitabin/Carboplatin) in patients with operable, high-risk, localized urothelial carcinoma of the upper urinary tract. iNDUCT - GETUG V08
Status
Recruiting
Phase
Phase 2
People taking part
50 people, planned
Started
28 Nov 2024
Planned end
28 Sept 2026
Type of study
Interventional
Record updated
28 November 2024

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with high-grade cancer of the renal pelvis or ureter that has not spread far, who can have kidney and ureter removal surgery.

Age
At least 18 years old. People older than 70 are checked for frailty with the G8 score; a G8 score below 14 cannot join.
Sex
All sexes can join.
Disease stage
High-grade urothelial carcinoma of the renal pelvis or ureter, confirmed by biopsy or urine cytology. Scans show no metastasis (M0) and either no lymph node disease or N1 disease (N1) on CT scan. Body weight above 30 Kg (66 lb) and ECOG performance status 0 to 1.
Earlier treatment
No earlier systemic therapy. The person must be able to have radical nephroureterectomy surgery.

Main reasons for not taking part

  • Muscle-invasive, in situ or high-grade non-muscle-invasive bladder cancer at the same time
  • NYHA class III or IV heart disease
  • Serious other illness, medical or psychiatric, including serious active infection
  • Active autoimmune disease needing systemic treatment, or immunodeficiency, or steroids or immunosuppressive therapy within 7 days before registration
  • History of HIV, or use of other investigational drugs

The registry criteria, word for word

Show all 15 criteriaShow less

Who can take part

  • The patient has a histologically-confirmed (ureteroscopic biopsy) or cytologically(urine cytology)-confirmed diagnosis of high-grade urothelial carcinoma of the renal pelvis or ureter. Presence of divergent histologies (i.e. squamous-cell tumor, adenocarcinoma, small cell carcinoma, micropapillary variant) may be acceptable provided that there is an important prevalence (> 90%) of urothelial component
  • Presence of either: o High-grade disease on ureteroscopic tumor biopsy OR o High-grade disease on urine cytology AND infiltrative aspect of renal pelvis/ureteral wall on CT imaging (presence of hydronephrosis will be considered invasive by definition) with negative cystoscopy. o In the absence of histological evidence, the opinion of the multidisciplinary consultation meeting (RCP) will prevail for the analysis of the imaging and the potential inclusion of the patient in the study
  • The patient is at least 18 years old. Patients older than 70 years will be evaluated for fragility with G8 score (Soubeyran et al. 2014). Patients with a G8 score of less than 14 will not be included in the study
  • Body weight > 30 Kg
  • No prior systemic therapies
  • Patient must be eligible to radical nephroureterectomy surgery
  • ECOG performance status 0 to 1
  • M0 No or N1 disease on CT scan

Who cannot take part

  • Concomitant diagnosis of muscle invasive or in situ or high grade non muscle invasive urothelial carcinoma of the bladder
  • Concomitant use of any other investigational drugs
  • Diagnosis of immunodeficiency or received systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to study registration
  • Evidence of NYHA functional class III or IV heart disease
  • Serious intercurrent medical or psychiatric illness, including serious active infection
  • Active autoimmune disease requiring systemic treatment within the past 3 months or a documented history of clinically severe autoimmune disease, or a syndrome that requires systemic steroids or immunosuppressive agents
  • History of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies)

Where in France

  • Centre Hospitalier Universitaire de NîmesNîmes, FranceTaking people

About the trial

What the trial wants to find out

To assess in each cohort and independently the pathological complete response (ypT0) rate of a combination therapy with neoadjuvant durvalumab and chemotherapy (Gemcitabine/Cisplatin or Carboplatin) before surgery in patients with high-risk, localized, non-metastatic urothelial carcinoma of the upper tract.

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record

Print a page for my doctor

Data and sources

Registry record
Listed on the EU's official list of trials (CTIS).
Official title
Safety and Efficacy of Neoadjuvant immunotherapy with Durvalumab (MEDI 4736) in combination with neoadjuvant chemotherapy (Gemcitabin/Cisplatin or Gemcitabin/Carboplatin) in patients with operable, high-risk, localized urothelial carcinoma of the upper urinary tract. iNDUCT - GETUG V08
Plain-language title
Tests durvalumab with chemotherapy before surgery in upper urinary tract cancerGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 9 November 2026.
Record updated
28 November 2024