Mesothelioma Clinical Trial
Official title:
Isolated Thoracic Perfusion With Hemofiltration (ITP-F) for Pretreated and Progressive Malignant Pleural Mesothelioma
This is an observational study of isolated thoracic perfusion with subsequent hemofiltration to lower the concentration of the cytotoxic drugs as a locoregional therapeutic strategy in malignant pleural mesothelioma.
Treatment of patients with progressive malignant pleural mesothelioma (MPM) after multimodal
therapy is a therapeutic challenge. Survival of the patients is low and the treatment
options are sparse. This is an observational study of isolated thoracic perfusion with
subsequent hemofiltration as a locoregional therapeutic strategy in this situation.
23 pts. with epithelioid MPM were included in this phase II study after informed consent.
All patients had progressive disease after multiple therapies and were recommended BSC of a
MDT. Following insertion of a venous and arterial 21 ch. stop flow catheter via a femoral
access, the inferior vena cava was blocked beneath the right atrium, the arterial catheter
was blocked in the aorta at the diaphragm. The upper arms were blocked by pneumatic cuffs.
Chemotherapy was given via the arterial catheter. Chemotherapy consisted of 60mg/m2
cisplatinum and 15mg/m2 mitoxantrone q for 3 weeks until progress. After administration of
chemotherapy, thoracic perfusion with blocked stop-flow catheters was maintained for 15
minutes. After de-blocking of the catheters, hemofiltration was performed for 45 min. with
5l filtrate. The endpoint of the study was overall survival.Secondary endpoint was toxicity.
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Observational Model: Case Control, Time Perspective: Prospective
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