Taxotere, Cisplatin, and CPT-11 in Advanced Solid Tumor Malignancies
- Registration Number
- NCT00251407
- Lead Sponsor
- Dana-Farber Cancer Institute
- Brief Summary
The purpose of this study is to find the highest dose of the combination of taxotere, cisplatin and CPT-11, that can be given without causing severe side effects. We also want to test the safety of this drug combination and see what effects (good and bad) it has on patients with advanced cancer for which there is no known curable treatment.
- Detailed Description
* This is a Phase I clinical trial. We are unsure of the safest and most effective dose of the drugs and therefore are planning on treating 3-6 patients with a given dose before increasing to higher dose levels.
* Each patient will receive approximately two cycles of therapy. On day one and day eight, they will receive taxotere, cisplatin and CPT-11 intravenously. The cycle will begin again on day 22.
* The following tests and procedures will be performed: CAT scan prior to beginning therapy, after every 2 cycles of therapy, and at the end of the study; physical exam before each course of therapy; vital signs before and with each dose of therapy; routine blood tests before starting therapy and weekly during treatment; chest x-ray and echocardiogram before starting therapy and; toxicity assessment each week of therapy.
* Patients will remain on the study as long as their cancer responds to treatment and they do not have unacceptable side effects.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 46
- Histologically confirmed, incurable solid tumor malignancy
- 18 years of age or older
- ECOG performance status of < or = to 2
- Life expectancy of greater than 12 weeks
- WBC > 3,000/mm3
- ANC > 1,500/mm3
- Platelet count > 100,000/mm3
- Total bilirubin within normal limits
- SGOT < 2.5 x ULN
- Alkaline phosphatase < 4 x ULN
- Prior chemotherapy for the treatment of metastatic or recurrent cancer
- Prior radiotherapy to greater than or equal to 15% of bone marrow
- Prior pelvic radiation therapy
- Prior nitrosoureas or mitomycin C
- Myocardial infarction in the past 6 months
- Major surgery in past 2 weeks
- Uncontrolled serious medical or psychiatric illness
- Uncontrolled diarrhea
- Peripheral neuropathy > grade 1
- Pregnant or lactating women
- Clinically apparent central nervous system metastases or carcinomatous meningitis
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description taxotere, cisplatin, irinotecan Taxotere - taxotere, cisplatin, irinotecan CPT-11 - taxotere, cisplatin, irinotecan Cisplatin -
- Primary Outcome Measures
Name Time Method To assess the maximum tolerated dose of weekly taxotere, cisplatin and CPT-11 in patients with incurable solid tumor malignancies. 3 years
- Secondary Outcome Measures
Name Time Method To define the dose-limiting toxicities of the combination of drugs. 3 years
Trial Locations
- Locations (3)
Massachusetts General Hospital
🇺🇸Boston, Massachusetts, United States
Brigham and Women's Hospital
🇺🇸Boston, Massachusetts, United States
Dana-Farber Cancer Institute
🇺🇸Boston, Massachusetts, United States