Blinatumoab公司
医学
不利影响
内科学
肿瘤科
重症监护医学
梅德林
儿科
临床试验
特非那定
作者
Ya-Lei Hu,Yong-Feng Su,Yang Li,Xuan Zheng,An Wang,Yizhi Wang,Lei Xu,Chun-Ji Gao,Liangding Hu,D H Liu,Xiao-Ning Gao
出处
期刊:PubMed
[National Institutes of Health]
日期:2025-12-01
卷期号:33 (6): 1571-1576
标识
DOI:10.19746/j.cnki.issn.1009-2137.2025.06.004
摘要
OBJECTIVE: To evaluate the efficacy and safety of blinatumomab in adult patients with relapsed/refractory (R/R) or measurable residual disease (MRD) positive B-cell acute lymphoblastic leukemia (B-ALL) in the real world. METHODS: ), overall survival (OS), and disease-free survival (DFS), as well as drug-related adverse reactions. RESULTS: group. The median DFS of the two groups were not reached. Drug-related adverse reactions occurred in 22 patients, and pyrexia was the most common (13 cases). Grade ≥3 adverse reactions occurred in 15 patients, and neutropenia was the most common (9 cases). Cytokine release syndrome occurred in 6 patients, including 5 cases with grade 1 and 1 case with grade 3. No patients interrupted therapy or died due to drug-related adverse reactions. CONCLUSION: B-ALL with acceptable adverse reactions.
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