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Efficacy, safety, and pharmacokinetics of teclistamab in Chinese patients with relapsed/refractory multiple myeloma from the China cohort of MajesTEC‐1

医学 多发性骨髓瘤 药代动力学 队列 中国 耐火材料(行星科学) 肿瘤科 内科学 政治学 天体生物学 物理 法学
作者
Zhen Cai,Zhongjun Xia,Aili He,Yu‐Jun Dong,Yafei Wang,Aijun Liao,Yang Song,Juanjuan Song,Clarissa Uhlar,Katherine Chastain,Latisha Watkins,Xinchao Luo,Lin Huang,Zhuolu Niu,Natalia A. Quijano Cardé,Yue Guo,Hongmei Xu,Raluca Verona,Longen Zhou,Jingyun Li
出处
期刊:Cancer [Wiley]
卷期号:131 (1): e35665-e35665 被引量:9
标识
DOI:10.1002/cncr.35665
摘要

INTRODUCTION: Teclistamab, the first approved B-cell maturation antigen-directed bispecific antibody for treatment of triple-class exposed relapsed/refractory multiple myeloma, demonstrated deep, durable responses with a manageable safety profile in the pivotal MajesTEC-1 cohort (NCT03145181/NCT04557098). Efficacy, safety, and pharmacokinetics from the MajesTEC-1 China cohort are reported. METHODS: Patients received teclistamab 1.5 mg/kg subcutaneously weekly after step-up dosing; patients could switch to less frequent dosing with continued response. RESULTS: In the China cohort (N = 26; median age, 66 years; median prior lines of therapy, 5) 15-month median follow-up, overall response rates, very good partial response or better, and complete response or better (≥CR) were 76.9%, 76.9%, and 57.7%, respectively. Median time to first response and ≥CR were 1.4 and 6.3 months, respectively; among patients with ≥CR and have available MRD samples, MRD negativity was achieved in 14/15 (93.3%) patients. Median duration of response, progression-free survival, and overall survival were not reached; 12-month duration of response, progression-free survival, and overall survival rates were 78.5%, 68.0%, and 83.5%, respectively. The safety profile was consistent with the pivotal cohort. Although infections occurred in 96.2% of patients, incidence decreased over time with six patients experiencing infections for >12 to 18 months. There were no discontinuations because of adverse events and no dose reductions. Ten patients switched to less frequent dosing. Teclistamab serum concentrations were consistent with the pivotal cohort, with a slightly lower mean pharmacokinetics profile. CONCLUSIONS: Teclistamab demonstrated efficacy and safety profiles in the China cohort consistent with the pivotal cohort, supporting teclistamab as a promising treatment option for triple-class exposed relapsed/refractory multiple myeloma in China.
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