| Literature DB >> 32290739 |
Kyoungmin Lee1, Joo Young Ha1, Ah Ra Jung2, Yoon Sei Lee2, Sang-Wook Lee3, Jin-Sook Ryu4, Eun Jin Chae5, Kyung Won Kim5, Jooryung Huh6, Chan-Sik Park6, Dok Hyun Yoon1, Cheolwon Suh1.
Abstract
We evaluated real-world effectiveness and safety of CT-P10 (Truxima®) compared with originator rituximab in diffuse large B-cell lymphoma (DLBCL) treatment. Before and after the introduction of CT-P10 to our institute (November 2017), 221 newly-diagnosed DLBCL patients received rituximab with standard cyclophosphamide, vincristine, doxorubicin and prednisone. Patients received originator rituximab throughout (n = 95), switched from originator rituximab to CT-P10 (n = 36), or received CT-P10 throughout (n = 90). There were no significant differences between groups in overall response rate (91.6% vs 94.4% vs 96.7%, respectively; p = 0.403) or complete response rate (84.2% vs 77.8% vs 86.7%, respectively; p = 0.467). Kaplan-Meier survival curves also showed no significant differences in progression-free survival and overall survival between groups (log-rank p = 0.794 and p = 0.955, respectively). Safety profiles were comparable between treatment groups. These data support the ability of CT-P10 to successfully replace originator rituximab in DLBCL treatment and, given the lowered financial barrier, to improve the overall prognosis for DLBCL patients.Entities:
Keywords: CT-P10; Diffuse large B-cell lymphoma; Truxima®; biosimilar; real-world evidence; rituximab
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Year: 2020 PMID: 32290739 DOI: 10.1080/10428194.2020.1742906
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022