Trabectedin for Patients with Advanced Soft Tissue Sarcoma: A Non-Interventional, Retrospective, Multicenter Study of the Italian Sarcoma Group.
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Palmerini Emanuela, Sanfilippo Roberta, Grignani Giovanni, Buonadonna Angela, Romanini Antonella, Badalamenti Giuseppe, Ferraresi Virginia, Vincenzi Bruno, Comandone Alessandro, Pizzolorusso Antonio, Brunello Antonella, Gelsomino Fabio, Pas Tommaso De, Ibrahim Toni, Grosso Federica, Zanelli Francesca, Pantaleo Maria Abbondanza, Milesi Laura, Ciuffreda Libero, Ferrari Vittorio, Marchesi Emanuela, Quattrini Irene, Righi Alberto, Setola Elisabetta, Carretta Elisa, Picci Piero, Ferrari Stefano
Аннотация
The Italian Sarcoma Group performed this retrospective analysis of patients with advanced soft tissue sarcoma, pretreated with ≥1 anthracycline-based treatment, and treated with trabectedin every three weeks. Primary endpoint was to describe real-life use of trabectedin across Italy. Secondary endpoints included objective response rate (ORR) and safety. Overall, 512 patients from 20 Italian centers were evaluated. Leiomyosarcoma (37.7%)/liposarcoma (30.3%) were the most prevalent histological types (abbreviated as L-sarcoma). Patients received a median of four trabectedin cycles (range: 1-40), mostly as a second-line treatment (~60% of patients). The ORR was 13.7% superior (p < 0.0001) in patients with L-sarcoma compared with patients with non-L-sarcoma (16.6% vs. 9.0%). Median progression-free survival (PFS) was 5.1 months, whereas median overall survival (OS) was 21.6 months. Significantly better PFS and OS were observed in patients with L-sarcoma, those with objective responses and/or disease stabilization, treated in an early line and treated with reduced dose. Bone marrow toxicity (61.4%) and transaminase increases (21.9%) were the most common grade 3/4 adverse events. The results of this real-life study suggest that trabectedin is an active treatment, which is mostly given as a second-line treatment to patients with a good performance status and high-grade, metastatic L-sarcoma (clinical trial information: NCT02793050).