Malignant Mesothelioma Clinical Trial
Official title:
ONCONASE Plus Doxorubicin Versus Doxorubicin For Patients With Malignant Pleural or Peritoneal Mesothelioma Who Have Had No More Than One Prior Chemotherapy Regimen
RATIONALE: Drugs used in chemotherapy work in different ways to stop tumor cells from
dividing so they stop growing or die. It is not yet known whether Onconase plus doxorubicin
is more effective than doxorubicin alone in treating patients with malignant mesothelioma.
PURPOSE: This randomized phase III trial is studying doxorubicin alone to see how well it
works compared to doxorubicin and Onconase in treating patients with malignant mesothelioma.
OBJECTIVES:
- Compare the efficacy of doxorubicin with or without ranpirnase in patients with
malignant pleural or peritoneal mesothelioma.
- Compare the safety profile of these regimens in these patients.
- Compare the overall survival, progression-free survival, and quality of life of
patients treated with these regimens.
OUTLINE: This is a randomized, open-label, controlled, multicenter study. Patients are
stratified according to disease histology (epithelioid vs nonepithelioid) and CALGB groups
1-4. Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients receive ranpirnase IV over 30 minutes weekly followed by doxorubicin
IV. Treatment repeats every 3 weeks for at least 6 courses in the absence of disease
progression. Patients demonstrating evidence of clinical response or stable disease may
continue on maintenance therapy with ranpirnase as a single agent until disease
progression.
- Arm II: Patients receive doxorubicin as in arm I for up to 6 courses. Quality of life
is assessed.
PROJECTED ACCRUAL: A minimum of 300 patients will be accrued for this study.
;
Allocation: Randomized, Masking: Open Label, Primary Purpose: Treatment
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