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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04428554
Other study ID # 19 URO 15
Secondary ID
Status Recruiting
Phase Phase 2
First received
Last updated
Start date June 30, 2020
Est. completion date July 2028

Study information

Verified date January 2024
Source Institut Claudius Regaud
Contact Jonathan KHALIFA
Phone 05 31 15 54 01
Email khalifa.jonathan@iuct-oncopole.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a phase II, multicenter, randomized open-label and comparative study designed to evaluate whether local consolidative radiotherapy plus standard of care improves overall survival as compared to standard of care in patients with limited metastatic urothelial bladder cancer and without progression following the initial phase of first-line systemic therapy. Each patient will be followed during 4 years from the date of randomization.


Recruitment information / eligibility

Status Recruiting
Enrollment 130
Est. completion date July 2028
Est. primary completion date July 2028
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Age = 18 years 2. Eastern Cooperative Oncology Group (ECOG) performance status = 2 3. Urothelial bladder cancer histologically proven (both pure urothelial cancers and mixed histologic features are allowed) 4. Metastatic patients (AJCC v8: M1a or M1b) documented with contrast-enhanced CT-scanner of the chest, abdomen and pelvis, either de novo or presenting first distant relapse following cystectomy (with no local recurrence in the cystectomy bed) 5. Completion of the initial phase (4-6 cycles) of 1st line metastatic treatment (systemic therapy by chemotherapy and/or immunotherapy by immune check-point inhibitor according to standard recommendations). Patients having started maintenance therapy are eligible. 6. No disease progression after the initial phase of first-line metastatic systemic therapy according to RECIST v1.1 7. No more than 3 residual metastatic lesions following the initial phase of first-line metastatic systemic therapy: 1. The number of residual lesions is determined on the basis of the imaging modality for tumor response assessment performed after systemic treatment according to local habits (CT-scan or 18FDG PET-CT if performed): In case of response assessment by CT-scanner only: residual lesions are all remaining visible lesions In case of response assessment by additional 18FDG PET-CT: residual lesions are only the lesions with residual hyperfixation 2. Regarding distant lymph nodes metastases: If evaluation is performed by CT-scanner only, residual lymph nodes are considered pathological according to one or several criteria among: - Short axis = 1cm - Central necrosis - Heterogeneous contrast enhancement Residual para-aortic nodes involvement accounts for one lesion, even if several para-aortic nodes are involved. Other nodes: each involved node accounts for one lesion. 8. Residual metastases (if applicable) eligible for SBRT in terms of dose constraints to the organs at risk, with no prior radiotherapy interfering with SBRT 9. 8 weeks or less between last cycle of the initial phase of systemic treatment and randomization 10. No contraindication to pelvic radiotherapy 11. Signed informed consent 12. Patient able to participate and willing to give informed consent prior performance of any study-related procedures and to comply with the study protocol 13. Patient affiliated to a Social Health Insurance in France. Exclusion Criteria: 1. Non-transitional cell histology (Squamous cell carcinoma, adenocarcinoma or neuroendocrine carcinoma of the bladder) 2. Brain metastases before systemic treatment 3. Liver metastases before systemic treatment 4. Absence of target to be irradiated (i.e. previous cystectomy + no residual lesions following systemic treatment + no pelvic or para-aortic nodes at metastatic presentation) 5. Patient with relapse following definitive chemoradiation of the bladder 6. Local recurrence in the cystectomy bed following cystectomy 7. Previous pelvic irradiation 8. Prior radiotherapy near the residual metastatic lesions precluding ablative SBRT 9. Active inflammatory bowel disease 10. Contraindication to SBRT of a lesion due to organ dysfunction; in particular, patients with lung lesions and documented or suspected interstitial lung disease should not be included 11. History of scleroderma 12. Current or past history of second neoplasm diagnosed within the last 5 years (except basocellular carcinoma and prostate cancer incidentally discovered during previous cystoprostatectomy and pelvic lymph node dissection and with a good prognosis [T stage <pT3b and Gleason <8 and pN- and post-operative PSA <0.1 ng/mL]) 13. Pregnancy or breast feeding or inadequate contraceptive measures 14. Known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial 15. Any psychological, familial, geographic or social situation, according to the judgment of investigator, potentially preventing the provision of informed consent or compliance to study procedure 16. Patient who has forfeited his/her freedom by administrative or legal award or who is under legal protection (curatorship and guardianship, protection of justice) 17. Concurrent enrolment in another interventional therapeutic clinical study

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
Experimental arm
Consolidative radiotherapy (pelvic irradiation and/or metastases irradiation) + standard of care +/- previous transurethral resection of bladder tumor

Locations

Country Name City State
France Clinique Claude Bernard Albi
France Institut de Cancerologie de L'Ouest Angers
France CHU Besançon Besançon
France Institut Bergonie Bordeaux
France Chu Morvan Brest
France Clinique Pasteur-Lanroze Brest
France Centre Francois Baclesse Caen
France Centre Jean Perrin Clermont-Ferrand
France Institut Andrée Dutreix Dunkerque
France Centre Oscar Lambret Lille
France Institut Paoli-Calmettes Marseille
France Centre Antoine Lacassagne Nice
France Institut Curie Paris
France Groupement de Radiothérapie et d'Oncologie des Pyrénées Pau
France Institut de Cancerologie de L'Ouest Saint-Herblain
France HIA Bégin Saint-Mandé
France Institut de Cancerologie Lucien Neuwirth Saint-Priest-en-Jarez
France Institut Universitaire du Cancer Toulouse Oncopole Toulouse
France Institut Gustave Roussy Villejuif

Sponsors (1)

Lead Sponsor Collaborator
Institut Claudius Regaud

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall Survival 4 years for each patient
Secondary Progression Free Survival 4 years for each patient
Secondary Safety will be assessed by the toxicity grading of the National Cancer Institute (NCI-CTCAE v5) 4 years for each patient
Secondary Quality of life will be evaluated by the EORTC QLQ-C-30 questionnaire 4 years for each patient
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