Bladder Transitional Cell Carcinoma Stage IV Clinical Trial
— JASINT1Official title:
Randomized Phase II Study Assessing the Combination of Vinflunine With Gemcitabine and Vinflunine With Carboplatin in Patients Ineligible to Cisplatin With Advanced or Metastatic Transitional Cell Carcinoma of the Urothelium
This study is assessing the combination of well known cytotoxics with a novel anti-cancer agent that could be administered as monotherapy without renal toxicity in patients with renal impairment presenting with advanced or metastatic urothelial carcinoma previously treated with a platinum-based regimen. The intent of this study is to clarify the benefit/risk ratio of the two most promising associations of cytotoxics including the novel therapeutic agent, vinflunine: vinflunine-gemcitabine and vinflunine-carboplatin.
| Status | Completed |
| Enrollment | 69 |
| Est. completion date | April 2014 |
| Est. primary completion date | October 2013 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years to 79 Years |
| Eligibility |
Inclusion Criteria: - Man or woman aged = 18 years and < 80 years - Signed written informed consent - Histologically confirmed diagnosis of locally advanced or metastatic predominantly transitional cell carcinoma of the urothelium (TCCU) - Ineligibility for cisplatin-based therapy because of at least one of the following two medical conditions: - Calculated creatinine clearance (Cockcroft-Gault formula)< 60 mL/min - New York Heart Association Classification Stage II-III Congestive Heart Failure (documented by medical history) - "Measurable" disease with at least one uni-dimensional lesion according to RECIST guideline (version 1.1) - ECOG performance status of 0 or 1 - Estimated life expectancy of at least 12 weeks - Patient without prior systemic anticancer therapy unless if it had been administered as neoadjuvant or adjuvant chemotherapy (CT) for TCCU and if the patient has documented relapse = 6 months after the last dose of CT (prior intravesical CT allowed) - Adequate bone marrow and hepatic functions as evidenced by: - Absolute Neutrophil Count = 2,000/mm3 (= 2.0 x 109/L) - Haemoglobin = 10 g/dL - Platelet count = 100,000/mm3 - Serum total bilirubin = 1.5 x upper limit of normal (ULN) - Transaminases = 2.5 x ULN [= 5 x ULN only in case of liver metastasis] - Absence of psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; these conditions should be assessed with the patient before registration in the trial Exclusion Criteria: - ECOG performance status = 2 - Woman if pregnant or lactating or with positive pregnancy test at inclusion; woman of child-bearing potential who did not use or is unwilling or unable to use an acceptable method to avoid pregnancy during the 2 months preceding the start of study treatment, for the entire study period and for up to 3 months after the last dose of study treatment; sexually active fertile man not using effective birth control during the study and up to 6 months after the last dose of study treatment if his partner is a woman of child-bearing potential - Known brain metastasis or leptomeningeal involvement. - Peripheral neuropathy Grade = 2 by NCI CTC - Prior radiation to = 30% of the bone marrow or completed < 30 days ago or without full recovery of toxicities - Other serious illness or medical condition including: - Infection requiring systemic anti-infective therapy - Any medical condition that might not be controlled, for instance patients with unstable angina, patients with myocardial infarction within 6 months or uncontrolled diabetes - Prior systemic chemotherapy for advanced or metastatic disease or neoadjuvant/adjuvant chemotherapy that was completed < 6 months before documented progression - Patient who had received any other investigational drug or anti-cancer therapy within 30 days before randomisation - Other malignancies except adequately treated basal carcinoma of the skin, in-situ cervix carcinoma, localised prostate cancer with limited risk of recurrence (pT = 2b, Gleason score = 7) that was incidentally discovered and did not lead to any other treatment apart from prostatectomy, or any other tumor with a disease free interval = 5 years - Inadequate renal function defined by a serum creatinine clearance < 30 mL/min (Cockcroft-Gault formula) - Known hypersensitivity to the study drugs or to drugs with similar chemical structures - Patients who require treatment with ketoconazole, itraconazole, ritonavir, amprenavir, indinavir, rifampicin (any potent CYP3A4 inhibitor or inducer) or phenytoin - Any concurrent chronic system immune therapy or previous organ allograft - Electrocardiogram (ECG) with significant modifications suggesting a high risk of occurrence of an acute clinical event |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| France | Pierre Fabre Research Institute | Boulogne |
| Lead Sponsor | Collaborator |
|---|---|
| Pierre Fabre Medicament |
France,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Disease control rate as defined by RECIST criteria (version 1.1) as a percentage of best overall responses of Complete (CR) + Partial (PR) + Stable Disease (SD) for both Vinflunine-Gemcitabine and Vinflunine-Carboplatin combinations | Assessment of lesions (measurable and non-measurable) should be performed at baseline and every 6 weeks (assessment interval). Evaluable patients: all baseline lesions must have been assessed at least once after the second cycle (6 weeks); patients who progress before the first evaluation will be considered as early progression. Primary analysis is planned on the intent to treat population, secondary analysis being performed on the evaluable population. |
Change from baseline in tumor assessment at 12 weeks (cycle 4) | No |
| Secondary | Tumor Response Rate as defined by RECIST criteria (version 1.1) with a best response as Complete (CR) or Partial (PR) | Assessment of lesions (measurable and non-measurable) should be performed at baseline and every 6 weeks (assessment interval). Evaluable patients: all baseline lesions must have been assessed at least once after the second cycle (6 weeks); patients who progress before the first evaluation will be considered as early progression. |
Change from baseline in tumor assessment at 12 weeks (cycle 4) | No |
| Secondary | Duration of Disease control in Participants With Best Response of CR + PR + SD | Tumor assessment at baseline and then every 6 weeks, until tumor progression. Duration of disease control according to investigator will be calculated among the responders and stable patients from the date of randomisation until the documentation of progression or death due to any cause. Patients who are lost to follow-up without progression, or reach the time point of analysis without a known record of progression or death will have the duration of disease control censored at the date of last tumour assessment or last contact of a follow-up showing no progression, whichever occur last. | From the date of randomisation until the date of documented progression or date of death due to any cause, assessed up to 10 months | No |
| Secondary | Duration of Response in Participants With Best Response of CR or PR | Tumor assessment at baseline and then every 6 weeks, until tumor progression. Duration of response will be calculated among the responders (i.e. CR and PR) . Patients who are lost to follow-up, or reach the time point of analysis without a known record of progression or death will have the duration of response censored at the date of last tumour assessment or last contact of a follow-up showing no progression, whichever occur last. | From the date that measurement criteria are first met for complete or partial response until the date of documented progression or date of death due to any cause, assessed up to 10 months | No |
| Secondary | Time to First Response calculated among the responders | Tumor assessment at baseline and then every 6 weeks. Will be calculated among the responders (i.e. CR and PR) | From the date of randomisation up to the first report of documented response, assessed up to 12 weeks (cycle 4). | No |
| Secondary | Time to Treatment Failure | Tumor assessment (RECIST) every 6 weeks. Patients who reach the time point of analysis without failure as defined above will have the time to treatment failure censored at the date of last tumour assessment or last contact of a follow-up not showing progression. Patients who discontinued treatment for other reason and who are lost to follow-up will be censored at the date of last contact. | From the date of randomisation until tumor progression, unacceptable toxicity, withdrawal of patient consent, lost to follow-up or start of new anticancer therapy, assessed up to 10 months. | No |
| Secondary | Progression Free Survival | Tumor assessment every 6 weeks (RECIST).Patients who are lost to follow-up, or reach the time point of analysis without a known record of progression or death will have the progression-free survival censored at the date of last tumour assessment or last contact of a follow-up showing no progression, whichever occur last. | From the date of randomisation until the date of progression or the date of death from any cause if no progression was recorded before, median patient follow-up of 11 months | No |
| Secondary | Overall Survival | Data recording every 3 months. For patients who have not died, survival time will be censored at the date of last news (i.e: date of last administration, tumor assessment, clinical examination, haematological or biochemistrical assessment or date of last contact). | From the time of randomisation up to death or last follow-up, assessed with a median patient follow-up of 15 months (assessed up to 24 months) | No |
| Secondary | Number of Participants With Serious Adverse Events (SAEs), Adverse Events (AEs) and AEs Leading to Discontinuation | Population: all treated patients unless the patient is lost to follow-up immediately after the start of the treatment. The patients will be analysed in the treatment arm they actually received. The NCI-CTC classification version 2.0 will be used to classify toxicities. Maximum grade or severity will be reported by cycle and by patient for each MedDRA Preferred Term. Analyses will be performed both regardless the relationship to treatment and related to treatment. Biochemical toxicities: the worst CTCAE version 2.0 grade will be analysed according to the grade present at baseline. |
AE and SAE will be collected up to 30 days after the last treatment administration, on an expected average period of 17 weeks | Yes |