Phase III multicenter randomized trial of amifostine as cytoprotectant in first-line chemotherapy in ovarian cancer patients

Open Access
Publisher Website
Google Scholar
Abstract
Background: A phase III multicenter randomized trial has been designed in order to address whether amifostine (WR-2721, Ethyol), an organic thiophosphate cytoprotector, can protect ovarian cancer patients from toxicity induced by carboplatin–paclitaxel chemotherapy. Patients and methods: Patients were randomly assigned to receive carboplatin [area under the curve (AUC) 5 mg·min/ml] and paclitaxel (175 mg/m2) with (arm A) or without (arm B) amifostine (910 mg/m2) every 21 days for six cycles. Results: One-hundred and eighty-seven patients were accrued: 93 patients in arm A and 94 patients in arm B. There was no difference in terms of erythrocytopenia between the two arms; grade 3–4 thrombocytopenia was higher in arm A (3.3% versus 0.6%; P = 0.0010). There was no significant reduction of grade 3–4 leukopenia in arm A (11.8% versus 13.8%). The incidence of grade 3–4 neutropenia was lower in arm A (31.3% versus 37.9%; P = 0.03), as was the incidence of severe mucositis (4.7% versus 15.4% in arm A versus arm B, respectively; P P = 0.02). With a median follow-up of 24 months (range 2–41), time to progression was similar between the two groups. Conclusions: We showed that amifostine can exert some protection from the cumulative toxicity associated with this regimen. The results need to be confirmed in other randomized trials with this combination.