Lung Cancer Clinical Trial
Official title:
Phase III Randomized Study of Paclitaxel and Carboplatin or Cisplatin Followed by Radiotherapy With or Without Concurrent Paclitaxel in Patients With Unresectable Stage III Non-Small Cell Lung Cancer
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 paclitaxel may make tumor cells more sensitive to radiation therapy. It
is not yet known if combination chemotherapy followed by radiation therapy is more effective
with or without paclitaxel in treating unresectable stage III non-small cell lung cancer.
PURPOSE: Randomized phase III trial to compare the effectiveness of combination chemotherapy
followed by radiation therapy with or without paclitaxel in treating patients who have
unresectable stage III non-small cell lung cancer.
OBJECTIVES:
- Compare the overall survival rate of patients with unresectable stage III non-small
cell lung cancer treated with paclitaxel and carboplatin or cisplatin followed by
radiotherapy with or without concurrent paclitaxel.
- Compare the 1-year survival rate and mean survival time in patients treated with these
regimens.
- Compare the objective response rate and local control in patients treated with these
regimens.
- Compare the tolerability of these regimens in these patients.
- Compare the safety profile and toxicity of these regimens in these patients.
OUTLINE: This is a randomized, multicenter study. Patients are randomized to 1 of 2
treatment arms.
All patients receive paclitaxel IV over 3 hours followed by carboplatin IV over 30 minutes
or cisplatin IV on day 1. Treatment repeats every 21 days for 2 courses. Patients then
proceed to randomized treatment.
- Arm I: Patients receive paclitaxel IV over 1 hour on day 1 and radiotherapy on days 1-5
of each week for 6 weeks.
- Arm II: Patients receive radiotherapy 5 days a week for 7 weeks. Patients are followed
every 3 months for 1 year, every 6 months for 3 years, and then annually thereafter.
PROJECTED ACCRUAL: A total of 300 patients (150 per treatment arm) will be accrued for this
study within 3 years.
;
Allocation: Randomized, Primary Purpose: Treatment
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