Mesothelioma Clinical Trial
Official title:
Phase I/II Trial of Carboplatin, Bevacizumab and Pemetrexed in the First-Line Treatment of Patients With Malignant Pleural Mesothelioma (MPM)
The purpose of this research study was to evaluate how effective the combination of
Carboplatin, Bevacizumab (Avastin™) and, Pemetrexed (Alimta™) is in the treatment of
patients with Malignant Pleural Mesothelioma (MPM). A combination of cisplatin and
pemetrexed is considered standard for this disease and typically off protocol patients would
receive cisplatin or carboplatin and pemetrexed as standard of care.
The planned length of the study (first patient screened to last patient enrolled) was 24
months. The planned length of the entire study (enrollment period + the treatment period + a
follow-up period of at least 12 months) was 36 months.
This was a planned Phase I/II dose escalation study. Patients were enrolled in a cohort of
3.
Eligible patients with unresectable pleural mesothelioma received frontline treatment
consisting of carboplatin AUC 5, bevacizumab 15 mg/kg, and pemetrexed 500 mg/m^2 every 21
days (Tier-1). Dose escalation continued to achieve a target dosage using carboplatin AUC 6
(Tier-2). After a maximum of 6 treatment cycles, non-progressing patients received
maintenance therapy with bevacizumab and pemetrexed every 21 days to complete 1-year total
treatment duration.
;
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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