Switch-Maintenance Gemcitabine After First-Line Chemotherapy In Patients With Malignant Pleural Mesothelioma
Malignant Pleural Mesothelioma
About this trial
This is an interventional treatment trial for Malignant Pleural Mesothelioma focused on measuring Mesothelioma, Switch-maintenance, Gemcitabine
Eligibility Criteria
Inclusion Criteria: Being at least 18 years old Histologically or cytologically confirmed unresectable malignant pleural mesothelioma ECOG Performance status 0-2 Completed at least four cycles of first line platinum (cisplatin or carboplatin) and pemetrexed combination chemotherapy before study entry No evidence of disease progression following first-line treatment based on radiological criteria. Adequate organ function is mandatory, defined as haemoglobin of at least 8.5 mg/dl, platelets of at least 100×10⁹ per L, and neutrophils of at least 1×10⁹/L. Exclusion Criteria: Progression of disease after first line Pregnant females ECOG Performance 3-4 Patients with sarcomatoid mesothelioma Patients who are candidates for curative surgery
Sites / Locations
- Ain Shams University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Other
Gemcitabine + supportive care
supportive care
Administration of maintenance gemcitabine (1000 mg/m²) on days 1 and day 8, in cycles of 21 days plus supportive care.
best supportive care alone.