Status: Finalised
First registered on:
15/09/2015
Last updated on:
11/05/2022
1. Study identification
EU PAS Register NumberEUPAS10391
Official titleFollow-Up of Jevtana® in real lIfe
Study title acronymFUJI
Study typeObservational study
Brief description of the studyProstate cancer is the most common cancer in France; it evolves slowly but there is a poor prognosis at the metastatic stage. Several therapeutic strategies are available such as hormonal therapies and chemotherapies. Cabazitaxel is a new taxane that has an European marketing authorization since March 2011 and indicated in the treatment of patients with metastatic castration-resistant prostate cancer previously treated with docetaxel. The availability of this treatment is recent (Dec 2012) and there is only limited data on the use, safety, and effectiveness of cabazitaxel in real-life practice. In this context, French health authorities request a French multicentre observational study. A retrospective cohort will be implemented with 400 patients initiating cabazitaxel from Sept 2013 to Aug 2015, followed 18 months and a prospective cohort with 60 patients initiating cabazitaxel from Mar 2016 to 28 Feb 2017, followed 6 months. The primary objective of the study is to evaluate the overall survival in the whole cohort and by treatment lines. The secondary objectives are to evaluate the safety, quality of life (QoL) and pain in the prospective cohort, to describe analgesic use, the characteristics of the treated study cohort and the conditions of cabazitaxel use in a real-life setting and to evaluate progression-free survival (PFS). The study will be conducted with participation of hospital pharmacists and physicians. A retrospective identification of patients will be performed by pharmacists from hospital pharmacy registers in order to avoid prescriber’s selection. Data collection will be performed by coordinating centre CRAs from the patient's medical records using an e-CRF. The QoL in the prospective cohort will be assessed using the FACT-P QoL questionnaire and pain will be evaluated by the Brief Pain Questionnaire - Short form (BPI-SF); these questionnaires will be completed by patients before each cabazitaxel infusion, up to the last cabazitaxel infusion.
Was this study requested by a regulator?Yes: France, Comité Economique des Produits de Santé (CEPS)
Is the study required by a Risk Management Plan (RMP)?
Not applicable
Regulatory procedure number (RMP Category 1 and 2 studies only)
Other study registration identification numbers and URLs as applicable
2. Research centres and Investigator details
Coordinating study entity
Department/Research grouppharmacoepidemiology
Organisation/affiliationUniversity of Bordeaux
Details of (Primary) lead investigator
Title Professor
Last name Moore
First name Nicholas
Is this study being carried out with the collaboration of a research network?
No
Other centres where this study is being conducted
Multiple centres
In total how many centres are involved in this Study?45
Countries in which this study is being conducted
National study
France
3. Study timelines: initial administrative steps, progress reports and final report
PlannedActual
Date when funding contract was signed06/01/2015
Start date of data collection30/10/2015
Start date of data analysis09/06/2017
Date of interim report, if expected28/08/2017
Date of final study report27/03/2018
4. Sources of funding
Please provide estimates of the percentage of funding by source for this study
Names(s)Approximate % funding
Pharmaceutical companiesSanofi100
Charities
Government body
Research councils
EU funding scheme
5. Contact details for enquiries
Scientific Enquiries
Title Mrs
Last name Fourrier-Réglat
First name Annie
Address line 1146 Rue Leo Saignat
Address line 2Service de Pharmacologie
Address line 3Université de Bordeaux - case 36
CityBordeaux
Postcode33076
CountryFrance
Phone number (incl. country code)33557574657
Alternative phone number33557571560
Fax number (incl. country code)
Public Enquiries
Title Mrs
Last name Fourrier-Réglat
First name Annie
Address line 1146 Rue Leo Saignat
Address line 2
Address line 3
CityBordeaux
Postcode
CountryFrance
Phone number (incl. country code)33557574657
Alternative phone number
Fax number (incl. country code)
6. Study drug(s) information
Substance class (ATC Code)L01CD04 (cabazitaxel)
7. Medical conditions to be studied
Medical condition(s)No
8. Population under study
Age
Adults (18 - 44 years)
Adults (45 - 64 years)
Adults (65 - 74 years)
Adults (75 years and over)
Sex
Male
9. Number of subjects
Estimated total number of subjects460
Additional information
400 patients for retrospective cohort and 60 patients for prospective cohort
10. Source of data
Is this study being carried out with an established data source?No
Sources of data
Prospective patient-based data collection
Pharmacy dispensing records
Medical charts, clinic charts, nurses’ notes, medical correspondence regarding the human subject, subject progress notes; Pathology reports; Laboratory reports; Study worksheets; Electronic hospital reporting system
Questionnaires Quality of life (FACT-P) and Pain (BPI-SF) directly completed by patients
11. Scope of the study
What is the scope of the study?
Drug utilisation study
Effectiveness evaluation
safety evaluation
Primary scope : Effectiveness evaluation
12. Main objective(s)
What is the main objective of the study?
To evaluate the overall survival of patients treated by cabazitaxel and according to treatment-line
Are there primary outcomes?Yes
Overall survival is defined as the interval between the date of first administration of cabazitaxel (inclusion date) and the date of death, irrespective of cause
Are there secondary outcomes?Yes
Safety based on data collected through medical file (NCI-CTCAE v4.0 toxicity scale and MEDdRA code); QoL and pain based on FACT-P and BPI-SF questionnaire. Description of analgesic use, patient's characteristics and cabazitaxel use. PFS defined as interval between inclusion date and date of progressive disease (radiological evaluation, RECIST criteria; clinical and biological parameters).
13. Study design
What is the design of the study?
Cohort study
14. Follow-up of patients
Will patients be followed up?Yes
Please describe duration of follow up
18 months per patient from initiation of cabazitaxel for retrospective cohort and 6 months per patient from initiation of cabazitaxel for prospective cohort.
15. Data analysis plan
Please provide a brief summary of the analysis method
A detailed statistical analysis plan (SAP) will be performed before database lock using SAS® software (latest current version).
The SAP will be validated by Scientific Committee. Descriptive statistics including mean, median, standard deviation, minimum, and maximum will be presented for continuous variables. For categorial variables, the number of subjects and percentage within each category will be presented.
Describing analyses will concern prescriber recruitment, baseline demographic and clinical characteristics at inclusion date, treatment pattern during follow-up after inclusion date, toxicities by patient, and quality of life, pain and analgesic consumption.
Overall and progression-free survival outcomes will be analysed using Kaplan Meier method and median survival will be reported with 95%CI (adjusted on previous treatment). Multivariate analysis will be using the Cox proportional hazard risk model to assess the factors associated with mortality and progression of disease.
16. ENCePP seal
Are you requesting the ENCePP seal for this study?
Yes
17. Full protocol
18. Study Results
Please list the 5 most relevant publications using data from your study
ReferenceLink to web-publication
Overall and progression-free survival with cabazitaxel in metastatic castration-resistant prostate cancer in routine clinical practice: the FUJI cohort.
Rouyer M, Oudard S, Joly F, Fizazi K, Tubach F, Jove J, Lacueille C, Lamarque S, Guiard E, Balestra A, Droz-Perroteau C, Fourrier-Reglat A, Moore N; FUJI Investigators.
Br J Cancer. 2019 Dec;121(12):1001-1008. doi: 10.1038/s41416-019-0611-6.https://doi.org/10.1038/s41416-019-0611-6
Quality Of Life And Pain During Treatment Of Metastatic Castration-Resistant Prostate Cancer With Cabazitaxel In Routine Clinical Practice.
Joly F, Oudard S, Fizazi K, Tubach F, Jove J, Lacueille C, Lamarque S, Guiard E, Balestra A, Droz-Perroteau C, Fourrier-Reglat A, Rouyer M, Moore N.
Clin Genitourin Cancer. 2020 Mar 6:S1558-7673(20)30037-9. doi: 10.1016/j.clgc.2020.02.003.https://doi.org/10.1016/j.clgc.2020.02.003
19. Other relevant documents
Other documents
DescriptionDocumentLatest version
Signed Code of
Conduct Checklist
Submitted
Signed Code of Conduct Declaration
Submitted
Signed Checklist for Study
Protocols
Submitted
