Logo Logo
Hilfe
Hilfe
Switch Language to English

Fukuhara, Noriko; Kato, Koji; Goto, Hideki; Takeshi, Tajima; Kawaguchi, Mayu; Tokushige, Kota; Akashi, Koichi; Teshima, Takanori; Harigae, Hideo; Schuster, Stephen J.; Thieblemont, Catherine; Dreyling, Martin und Fowler, Nathan (2022): Efficacy and safety of tisagenlecleucel in adult Japanese patients with relapsed or refractory follicular lymphoma: results from the phase 2 ELARA trial. In: International Journal of Hematology, Bd. 117, Nr. 2: S. 251-259

Volltext auf 'Open Access LMU' nicht verfügbar.

Abstract

Background Tisagenlecleucel yielded a high durable response rate in patients with relapsed/refractory (r/r) follicular lymphoma (FL) in the global phase 2 ELARA trial. Here, we report the efficacy, safety, and cellular kinetics of tisagenlecleucel in a subgroup of Japanese patients with r/r FL from ELARA. Methods ELARA (NCT03568461) is a global single-arm trial of tisagenlecleucel in patients with r/r FL who received >= 2 prior lines of therapy. The primary endpoint was the complete response rate (CRR), and the secondary endpoints were the overall response rate, duration of response, progression-free survival, overall survival, safety, and cellular kinetics. Results As of March 29, 2021, nine Japanese patients were enrolled and received tisagenlecleucel with a median follow-up of 13.6 months (range, 10.5-19.3). Per independent review committee, CRR was 100% (95% CI 63.1-100). Within 8 weeks of infusion, cytokine release syndrome (CRS) of any grade was reported in 6 patients (66.7%);however, no grade >= 3 CRS or any grade serious neurological events or treatment-related deaths were observed. Conclusion Tisagenlecleucel showed high efficacy and manageable safety in adult Japanese patients with r/r FL. Moreover, the clinical outcomes were similar to the global population, which supports the potential of tisagenlecleucel in Japanese patients with r/r FL.

Dokument bearbeiten Dokument bearbeiten