Selective pulmonary artery perfusion with melphalan is equal to isolated lung perfusion but superior to intravenous melphalan for the treatment of sarcoma lung metastases in a rodent model.

摘要

Isolated lung perfusion (ILuP) and selective pulmonary artery perfusion (SPAP) are experimental surgical techniques to deliver high-dose chemotherapy selectively to the lung for the treatment of lung metastases. ILuP with melphalan (MN) has shown to be feasible in clinical studies but can only be used once because it is invasive. SPAP as an endovascular technique can be repeated several times, but no results have been reported so far. Pharmacokinetics and efficacy of SPAP with MN were studied in a rodent lung metastasis model and compared it with ILuP and intravenous (IV) therapy.Pharmacokinetics: forthy-five Wag-Rij rats were randomized into three groups: IV 0.5?mg MN, ILuP 0.5?mg MN and SPAP 0.5?mg MN. Every treatment group was again randomized in three groups: 15?min treatment, 30?min treatment and 30?min treatment with 30?min reperfusion. Blood and tissue samples were taken for MN concentrations. Efficacy: twenty-five Wag-Rij rats were randomized into five groups: control, sham thoracotomy, IV 0.5?mg MN, ILuP 0.5?mg MN and SPAP 0.5?mg MN. At day 0, bilateral lung metastases were induced, and treatment followed at day 7. At day 28, rats were sacrificed and pulmonary metastases counted. Survival: thirty Wag-Rij rats were randomized into five groups: control, sham ILuP, IV 0.5?mg MN, ILuP 0.5?mg MN, SPAP 0.5?mg MN. At day 0, left-sided lungmetastases were induced with treatment at day 7. Endpoints were death due to disease or survival up to 90 days.Pharmacokinetics: SPAP and ILuP resulted in significantly higher left lung MN concentrations compared with IV (P?=?0.05). Efficacy: SPAP (30?±?22 nodules) and ILuP (20?±?9 nodules) resulted in significantly less nodules compared with IV (113?±?17 nodules; P?