Trial of Weekly Taxotere and Irinotecan (CPT-11) in Patients With Advanced Non-small Cell Lung Cancer

NCT ID: NCT00819728

Last Updated: 2011-01-11

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 35 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2000-06-30
• Study Completion Date: 2003-01-31

Brief Summary

The main purpose of the study is to determine the activity of the weekly combination of docetaxel (Taxotere) and irinotecan in terms of response rate in subjects with advanced, previously untreated, non-small cell lung cancer. It is also to determine the activity of this combination in terms of response duration, time to progression, median survival, overall survival, and percent one-year survival, as well as the side-effect and toxicity profile of weekly Taxotere and weekly irinotecan.

Conditions

Carcinoma, Non-Small-Cell Lung

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Taxotere/Irinotecan

Group Type: EXPERIMENTAL

Docetaxel

Intervention Type: DRUG

35mg/m2 IV each week for 4 weeks

Irinotecan

Intervention Type: DRUG

50mg/m2 IV each week for 4 weeks

Interventions

Docetaxel

35mg/m2 IV each week for 4 weeks

Intervention Type: DRUG

Irinotecan

50mg/m2 IV each week for 4 weeks

Intervention Type: DRUG

Other Intervention Names

Taxotere

Eligibility Criteria

Inclusion Criteria

• Microscopically or cytologically confirmed non-small cell lung cancer. Histology may include large cell, squamous cell, undifferentiated, or bronchioalveolar carcinoma, or adenocarcinoma, but no small cell or carcinoid.
• Inoperable stage III B or metastatic stage IV NSCLC
• Measurable (bidimensionally) indicator lesion(s) which have not been irradiated.
• No prior systemic chemotherapy. Prior irradiation for NSCLC is permitted, however, the measurable or evaluable non-measurable disease must be completely outside the radiation portal or there must be radiologic proof of progressive disease. If a patient is receiving palliative radiation, other than the chest, to one site at 30 cGy or less, then the patient is eligible and chemotherapy can proceed immediately after palliative RT.
• ECOG performance status 0 or 1 at screening and on the first day of treatment
• Life expectancy = 12 weeks.
• Patients must be > 4 weeks from prior radiation therapy to the pelvis, spine or long bones, and must be recovered from all side effects.
• Patients must be > 3 weeks from prior major surgery, except for a simple biopsy or placement of a venous access device.

Exclusion Criteria

• No patient may have the following:
• Neutrophils < 1,500/mm3.
• Platelets < 100,000/mm3.
• Serum creatinine >1.8 mg/dL.
• SGOT > 1.5 times the upper limit of normal for institution.
• Total bilirubin > the upper limit of normal for institution.
• Alkaline phosphatase > 5 times the upper limit of normal for institution.
• Pregnant or lactating females or females of childbearing potential not employing adequate contraception.
• History of other malignancy within the last five years which could affect the diagnosis of NSCLC, except basal cell carcinoma of the skin or carcinoma in situ of the cervix.
• Current metastatic CNS disease, if present, must have been treated and clinically stable for at least 3 weeks prior to initial Taxotere treatment. Patients with documented meningeal carcinomatosis are not eligible.
• Grade 2 or greater peripheral neuropathy.
• Psychological, familial, sociological or geographical conditions which do not permit weekly medical follow-up and compliance with the study protocol.
• Patients who are medically unstable, including but not limited to active infection, acute hepatitis, gastrointestinal bleeding, uncontrolled cardiac arrhythmias, uncontrolled angina, uncontrolled hypercalcemia, uncompensated congestive heart failure, uncontrolled diabetes, dementia, seizures, superior vena cava syndrome, and patients whose circumstances do not permit completion of the study or the required follow-up.
• Patients with a history of hypersensitivity reaction to products containing Polysorbate 80 (Tween 80).
• Patients requiring concurrent treatment with corticosteroids unless chronic treatment (> 6 months) at low doses (< 20 mg/day of methylprednisolone or equivalent).
• Patients receiving an investigational drug within 3 weeks of registration.

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Sanofi

INDUSTRY

Sponsor Role: lead

Responsible Party

sanofi-aventis

Principal Investigators

Yasir Nagarwala, MD

Role: STUDY_DIRECTOR

Sanofi

Locations

Sanofi-Aventis US

Bridgewater, New Jersey, United States

Countries

United States

Other Identifiers

RP56976_US1_203

Identifier Type: -

Identifier Source: org_study_id