Clinical Trials Directory

Trials / Completed

CompletedNCT00004202

Combination Chemotherapy, Radiation Therapy, and RSR13 in Treating Patients With Stage III Non-small Cell Lung Cancer

A Phase II Study of Induction Chemotherapy With Paclitaxel and Carboplatin Followed by Radiation Therapy With RSR13 for Locally Advanced Inoperable Non-Small Cell Lung Cancer

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
Sponsor
Spectrum Pharmaceuticals, Inc · Industry
Sex
All
Age
18 Years – 120 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs such as RSR13 may make tumor cells more sensitive to radiation therapy. PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy, radiation therapy, and RSR13 in treating patients who have stage III non-small cell lung cancer that cannot be removed by surgery.

Detailed description

OBJECTIVES: I. Determine the one year survival rate, two year survival rate, and median survival rate in patients with locally advanced unresectable non-small cell lung cancer treated with paclitaxel and carboplatin followed by radiotherapy plus RSR13. II. Determine the complete and partial response rates and progression free interval in the chest (radiation portal) of these patients on this regimen. III. Determine the time to disease progression outside of the radiation portal in these patients on this regimen. IV. Determine the toxic effects and adverse events associated with this regimen in these patients. OUTLINE: This is a multicenter study. Induction chemotherapy: Patients receive paclitaxel IV over 3 hours and carboplatin IV over 30 minutes every 3 weeks for 2 courses. Radiotherapy: Beginning 3 to 4 weeks after induction chemotherapy, patients receive RSR13 IV over 30 minutes, followed by fractionated radiotherapy 5 times weekly for 6-7 weeks. Patients are followed monthly for 2 months and then every 3 months thereafter until disease progression or death. PROJECTED ACCRUAL: A total of 46-48 patients will be accrued for this study.

Conditions

Interventions

TypeNameDescription
DRUGcarboplatin
DRUGchemotherapy
DRUGefaproxiral
DRUGpaclitaxel
RADIATIONradiation therapy

Timeline

Start date
1998-10-01
Primary completion
2003-01-01
Completion
2003-01-01
First posted
2004-06-25
Last updated
2021-08-26

Locations

16 sites across 2 countries: United States, Canada

Source: ClinicalTrials.gov record NCT00004202. Inclusion in this directory is not an endorsement.