Literature DB >> 33751401

Efficacy and Safety of the Biosimilar IBI301 Plus Standard CHOP (I-CHOP) in Comparison With Rituximab Plus CHOP (R-CHOP) in Patients with Previously Untreated Diffuse Large B-Cell Lymphoma (DLBCL): A Randomized, Double-Blind, Parallel-Group, Phase 3 Trial.

Yuqin Song1, Hui Zhou53, Huilai Zhang3, Wei Liu4, Yuerong Shuang5, Keshu Zhou6, Fangfang Lv7, Hao Xu8, Jianfeng Zhou9, Wei Li10, Huaqing Wang11, Hongyu Zhang12, Haiwen Huang13, Qingyuan Zhang14, Wei Xu15, Zheng Ge16, Ying Xiang17, Shuye Wang18, Da Gao19, Shun'e Yang20, Jinying Lin21, Lin Wang22, Liqun Zou23, Meifang Zheng24, Jing Liu25, Zonghong Shao26, Ying Pang27, Ruixiang Xia28, Zhendong Chen29, Ming Hou30, Hongxia Yao31, Ru Feng32, Zhen Cai33, Mingzhi Zhang34, Wenhua Ran35, Lin Liu36, Shan Zeng37, Wei Yang38, Peng Liu39, Aibin Liang40, Xuelan Zuo41, Qingfeng Zou42, Junxun Ma43, Wei Sang44, Ye Guo45, Wei Zhang46, Yongqing Cao47, Yan Li48, Jifeng Feng49, Xin Du50, Xiaohong Zhang51, Hongguo Zhao52, Hui Zhou53, Jie Yu53, Xing Sun53, Jun Zhu54, Lugui Qiu55.   

Abstract

INTRODUCTION: Patients with diffuse large B-cell lymphoma (DLBCL) have limited access to rituximab. IBI301 is a recombinant chimeric murine/human anti-CD20 monoclonal antibody and is a candidate biosimilar to rituximab. This study aimed to assess the therapeutic equivalence of IBI301 and rituximab in previously untreated patients with diffuse large B-cell lymphoma (DLBCL).
METHODS: This multicenter, randomized, double-blind, parallel-group, phase 3 trial compared IBI301 and rituximab, both plus the chemotherapy of doxorubicin, cyclophosphamide, vindesine, and prednisone (CHOP), was conducted in 68 centers across China. Eligible patients with untreated CD20 positive (CD20+) DLBCL randomly received IBI301 (375 mg/m2) plus the standard CHOP or rituximab (375 mg/m2) plus the standard CHOP for six cycles of a 21-day cycle. The primary end point was the overall remission rate (ORR). Efficacy equivalence was defined if 95% CIs for the ORR difference between the two groups were within a ± 12.0% margin.
RESULTS: Between August 22, 2016, and September 5, 2018, 419 patients were randomly allocated into the IBI301 group (N = 209) and rituximab group (N = 210). In the full analysis set, the ORR was 89.9% and 93.8% in the IBI301 and rituximab groups, respectively, and the ORR difference was -3.9% (95% CI - 9.1%-1.3%), falling within a ± 12.0% margin. The occurrences of treatment-emergent adverse events (TEAEs) (100% vs. 99.0%) and AEs of grade ≥ 3 (87.1% vs. 83.3%) were similar in the two groups (P > 0.05).
CONCLUSIONS: IBI301 had a non-inferiority efficacy and a comparable safety compared with rituximab. IBI301 plus CHOP could be suggested as a candidate treatment regimen for untreated patients with CD20+ DLBCL. TRIAL REGISTRATION: This trial is registered on ClinicalTrials.gov (NCT02867566).

Entities:  

Keywords:  Biosimilar; CHOP; DLBCL; IBI301; Rituximab

Mesh:

Substances:

Year:  2021        PMID: 33751401     DOI: 10.1007/s12325-020-01603-8

Source DB:  PubMed          Journal:  Adv Ther        ISSN: 0741-238X            Impact factor:   3.845


  15 in total

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9.  Association of serum Rituximab (IDEC-C2B8) concentration and anti-tumor response in the treatment of recurrent low-grade or follicular non-Hodgkin's lymphoma.

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