Docetaxel and Lapatinib in Metastatic Transitional Cell Carcinoma in Bladder
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT01382706|
Recruitment Status : Terminated (Trial not progressing toward scientific goals)
First Posted : June 27, 2011
Last Update Posted : April 11, 2017
|Condition or disease||Intervention/treatment||Phase|
|Recurrent Bladder Cancer Stage III Bladder Cancer Stage IV Bladder Cancer Transitional Cell Carcinoma of the Bladder||Drug: docetaxel Drug: lapatinib ditosylate Other: immunohistochemistry staining method Genetic: fluorescence in situ hybridization Other: laboratory biomarker analysis||Phase 2|
I. To assess the efficacy of 1250 mg of lapatinib (lapatinib ditosylate) given in combination with docetaxel in prolonging progression-free survival of subjects with metastatic, previously treated transitional cell carcinoma (TCC) relative to historical controls.
I. To assess the efficacy of 1250 mg of Lapatinib given in combination with docetaxel in the objective response rates and overall survival.
II. To study the tolerability and safety of 1250 mg of lapatinib given in combination with docetaxel by assessing the incidence and nature of Grade 3, 4 and serious adverse events (AEs).
I. To assess the expression status of epidermal growth factor receptor (EGFR) or human epidermal growth factor receptor 2 (HER-2) in tumor tissue and/or circulating tumor cells (CTCs) as potential predictors of response to therapy.
II. To evaluate the number of CTC's present in 7.5mLs of peripheral blood as a predictor for disease progression and response of treatment in bladder cancer in the setting of combination therapy of lapatinib and docetaxel.
III. To evaluate the effect of lapatinib in human at molecular level by targeting the phosphorylation activity of the AKT/extracellular-regulated kinase (ERK) on pathway prior and during the treatment with lapatinib.
OUTLINE: Patients receive docetaxel intravenously (IV) over 1 hour on day 1 and lapatinib ditosylate orally (PO) once daily (QD) on days 1-21. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up every 6 months for up to 2 years.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||15 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Single Arm Phase II Study of Docetaxel and Lapatinib in Metastatic Transitional Cell Carcinoma in Bladder as Second Line Treatment|
|Actual Study Start Date :||June 13, 2011|
|Actual Primary Completion Date :||July 15, 2013|
|Estimated Study Completion Date :||December 15, 2017|
Patients receive docetaxel IV over 1 hour on day 1 and lapatinib ditosylate PO QD on days 1-21. Courses repeat every 21 days until disease progression or unacceptable toxicity.
Other Names:Drug: lapatinib ditosylate
Other Names:Other: immunohistochemistry staining method
Other Name: immunohistochemistryGenetic: fluorescence in situ hybridization
Other Name: fluorescence in situ hybridization (FISH)Other: laboratory biomarker analysis
- Progression-free survival rate [ Time Frame: At 12 weeks ]Defined as the time period from the start of treatment and documented progression or death without documentation of progression. Summarized with Kaplan-Meier curves. The median will be estimated using a non-parametric method.
- Objective response rates [ Time Frame: After 6 and 12 weeks and then every 9 weeks ]
- Overall survival [ Time Frame: Every 6 months for up to 2 years ]
- To study tolerability and safety by assessing the incidence and nature of Grade 3, 4 and serious adverse events [ Time Frame: Weeks 1, 4, 7, 10, 13, 16, 19, 22 and then every 6 months for up to 2 years ]
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): NCT01382706
|United States, California|
|USC/Norris Comprehensive Cancer Center|
|Los Angeles, California, United States, 90033|
|Principal Investigator:||David Quinn, M.D.||University of Southern California|