Docetaxel - Carboplatin as Second Line Treatment in Patients With Small Cell Lung Cancer (DOCAR)
|ClinicalTrials.gov Identifier: NCT00686985|
Recruitment Status : Unknown
Verified May 2008 by Jeroen Bosch Ziekenhuis.
Recruitment status was: Recruiting
First Posted : May 30, 2008
Last Update Posted : May 30, 2008
|Condition or disease||Intervention/treatment||Phase|
|Small Cell Lung Cancer||Drug: Carboplatin, docetaxel||Phase 2|
Hide Detailed Description
Small cell lung cancer (SCLC) is diagnosed in approximately 15 % of all the lung cancer cases. SCLC is recognized by its rapid tumor growth, with a high chemo- and radio sensitivity, and by its high metastasizing potential. Patients with extensive-stage disease have a 5-year survival rate of 1% to 2%.
Almost 2/3 of the patients have already extensive disease (ED) upon diagnosis.The recommended treatment of ED-SCLC is systemic chemotherapy, considered to be the standard first line treatment option in all patients with SCLC regardless of performance status and age. World-wide, the most commonly used regimen for 1st line treatment is the combination of cisplatin-etoposide, while in the Netherlands the cyclophosphamide, doxorubicin and etoposide regimen is widely used.Survival outcome with these regimens appear similar.
Unfortunately, relapses occur in all patients and responses to second-line chemotherapy have proven to be of short term. Until recently, there were no registered drugs for treatment of relapsing SCLC. Phase II studies with docetaxel in first line - and second line treatment of SCLC demonstrated that docetaxel is an active agent in these patient groups. Therefore docetaxel seems suitable for evaluation in combination with other cytotoxic drugs active in this disease. Until now no studies have been performed with a combination of docetaxel and platinum in this group of previously treated SCLC patients.
A phase II study in previously untreated patients with SCLC shows that the combination docetaxel and cisplatin/carboplatin is an active and well tolerated regimen in extensive SCLC.
To evaluate the anti-tumor activity of a docetaxel/carboplatin regimen in patients with refractory or relapsed SCLC. Furthermore to asses the safety profile of the docetaxel/carboplatin combination.
This study will be a open label non-randomized study conducted in patients with refractory or relapsed SCLC. It is a phase II study with 50 patients.
Docetaxel infusion 75 mg/m2, carboplatin AUC = 6 mg/ml·min day 1, every 21 days for 4-6 cycles.
Patients with histologically or cytologically proven SCLC at the first diagnosis with refractory or relapsed SCLC after first line treatment. Signed informed consent. Age > 18 years. WHO ps 0,1 or 2.
Primary endpoint: response rate. Secondary endpoint(s): time to progression, response duration, safety profile and survival.
Stress and risks for the patient:
Hospital visits and tests are not different from the standard treatment. Stress due to adverse events is not essential higher estimated. Special risks are not expected. Frequently medical examination and control of laboratory results will be done. Detailed instruction will be given about what do to in case of serious toxicity.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||55 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Phase II Study of Docetaxel - Carboplatin as Second Line Treatment in Patients With Refractory or Relapsed Small Cell Lung Cancer|
|Study Start Date :||September 2007|
|Estimated Study Completion Date :||July 2010|
Drug: Carboplatin, docetaxel
Carboplatin AUC 5, Docetaxel 75 mg/m2, q 3 weeks, 4-6 cycles, 12-18 weeks
- Response rate [ Time Frame: 2 yrs ]
- Time to progression; Response duration; Survival; Safety profile [ Time Frame: 2 yrs ]
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): NCT00686985
|Contact: B Biesma, Dr.||firstname.lastname@example.org|
|Contact: F.M.N.H. Schramel, Dr.||email@example.com|
|'s-Hertogenbosch, Brabant, Netherlands, 5211NL|
|Contact: B. Biesma, Dr. 31-073-699-2615 firstname.lastname@example.org|
|Contact: F. Schramel, Dr. 31-0609-9111 email@example.com|
|Sub-Investigator: H van der Heijden, Dr.|
|Sub-Investigator: J.N.H. Timmer - Bonte, Dr.|
|Sub-Investigator: H Smit, Dr.|
|Sub-Investigator: H.J.M. Groen, Prof. Dr.|
|Principal Investigator:||B Biesma, Dr.||Jeroen Bosch Ziekenhuis|