Affiliation:
1. From the Vall d'Hebron University Hospital; University Hospital del Mar-IMIM, Barcelona, Spain; Hopital Foch, Suresnes; Centre Oscar Lambret, Lille; Institut de Recherche Pierre Fabre, Boulogne; Hôpital Henri Mondor, Créteil, France; Marie Curie Institute, Warsaw; SPZ Pulmonologii Oddzial Onkologii, Olsztyn, Poland; City Polyprofile Hospital N2, Saint Petersburg; Medical Radiological Research Center, Kaluga Region, Russian Federation; Herlev University Hospital, Herlev; Rigshospitalet, Copenhagen,...
Abstract
Purpose Vinflunine (VFL) is a new microtubule inhibitor that has activity against transitional cell carcinoma of urothelial tract (TCCU). We conducted a randomized phase III study of VFL and best supportive care (BSC) versus BSC alone in the treatment of patients with advanced TCCU who had experienced progression after a first-line platinum-containing regimen. Patients and Methods The study was designed to compare overall survival (OS) between patients receiving VFL + BSC (performance status [PS] = 0: 320 mg/m2, every 3 weeks; PS = 0 with previous pelvic radiation and PS = 1: 280 mg/m2 subsequently escalated to 320 mg/m2) or BSC. Results Three hundred seventy patients were randomly assigned (VFL + BSC, n =253; BSC, n = 117). Both arms were well balanced except there were more patients with PS more than 1 (10% difference) in the BSC arm. Main grade 3 or 4 toxicities for VFL + BSC were neutropenia (50%), febrile neutropenia (6%), anemia (19%), fatigue (19%), and constipation (16%). In the intent-to-treat population, the objective of a median 2-month survival advantage (6.9 months for VFL + BSC v 4.6 months for BSC) was achieved (hazard ratio [HR] = 0.88; 95% CI, 0.69 to 1.12) but was not statistically significant (P = .287). Multivariate Cox analysis adjusting for prognostic factors showed statistically significant effect of VFL on OS (P = .036), reducing the death risk by 23% (HR = 0.77; 95% CI, 0.61 to 0.98). In the eligible population (n = 357), the median OS was significantly longer for VFL + BSC than BSC (6.9 v 4.3 months, respectively), with the difference being statistically significant (P = .040). Overall response rate, disease control, and progression-free survival were all statistically significant favoring VFL + BSC (P = .006, P = .002, and P = .001, respectively). Conclusion VFL demonstrates a survival advantage in second-line treatment for advanced TCCU. Consistency of results exists with significant and meaningful benefit over all efficacy parameters. Safety profile is acceptable, and therefore, VFL seems to be a reasonable option for TCCU progressing after first-line platinum-based therapy.
Publisher
American Society of Clinical Oncology (ASCO)