High-dose Chemotherapy With Autologous Stem Cell Transplantation in Poor Prognosis Germ-cell Tumors: TAXIF II
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|ClinicalTrials.gov Identifier: NCT00231582|
Recruitment Status : Completed
First Posted : October 4, 2005
Last Update Posted : February 25, 2011
High-dose chemotherapy (HD-CT) is able to circumvent platinum-resistance of resistant/refractory germ-cell tumors (GCTs), but expectancy of cure remains low. New strategies are needed with new drugs and a sequential approach.
Patients with relapsed (but not absolutely refractory to Cisplatinum-based chemotherapy) poor-prognosis GCTs are scheduled to receive 2 cycles combining epirubicin and paclitaxel followed by 3 consecutive HD-CT supported by stem cell transplantation. One course will combine Taxol, 360 mg/m² + thiotepa, 720 mg/m², followed by two ICE regimens (Ifosfamide, 12 g/m², carboplatin, AUC 20, etoposide, 1500 mg/m²).
This phase II study is designed as a Gehan method. The main objective of the study is the complete response rate. With this aim in view, it is planned to enroll in its first step 14 patients to insure that if no complete response (CR) is noticed, study would be stopped for inefficacy (i.e., a CR rate lower than 20%). If one or more CR are noticed, protocol specified that up to 45 patients will be included in order to reduce the confidence interval (CI) of the CR rate. Secondary objectives are the overall response rate (RR), the overall survival (OS) and the progression-free survival (PFS) rates, toxicity and toxic death rate. The statistical analysis is done in terms of intent-to-treat.
|Condition or disease||Intervention/treatment||Phase|
|Testicular Neoplasms||Drug: epirubicin Procedure: high-dose and autologous stem cell transplantation Drug: paclitaxel Drug: etoposide Drug: ifosfamide Drug: carboplatin||Phase 2|
Show Detailed Description
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||50 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Sequential High-Dose Chemotherapy Combining Two Mobilization and Cyto-Reductive Treatments Followed by Three High-Dose Chemotherapy Regimens Supported by Autologous Stem Cell Transplantation|
|Study Start Date :||September 2004|
|Actual Primary Completion Date :||January 2010|
|Actual Study Completion Date :||January 2010|
epirubicinProcedure: high-dose and autologous stem cell transplantation
high-dose and autologous stem cell transplantationDrug: paclitaxel
- Complete response rate [ Time Frame: during de study ]Complete response rate
- Survival (overall and progression-free), toxicity, toxic-death rate. [ Time Frame: during the study ]Survival (overall and progression-free), toxicity, toxic-death rate.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00231582
|Hôpital TENON, Service d'Oncologie Médicale|
|Paris, France, 75020|
|Principal Investigator:||Jean-Pierre LOTZ, Pr,MD,PhD||Assistance Publique - Hôpitaux de Paris|