威尼斯人
医学
内科学
养生
肿瘤科
微小残留病
临床终点
完全缓解
不利影响
化疗方案
化疗
急性淋巴细胞白血病
存活率
入射(几何)
白血病
意向治疗分析
儿科
生存分析
淋巴细胞白血病
前瞻性队列研究
标签外使用
临床试验
总体生存率
倾向得分匹配
儿童白血病
血液学
疾病
临床研究阶段
作者
Xiaoyuan Gong,Yuntao Liu,Qiuyun Fang,Runxia Gu,Kaiqi Liu,Dong Lin,Chunlin Zhou,Guangji Zhang,Benfa Gong,Shuning Wei,Yan Li,Shouyun Li,Ying Wang,Shaowei Qiu,B C Liu,Ying Wang,Yingchang Mi,Hui Wei,Jianxiang Wang
出处
期刊:Blood
[Elsevier BV]
日期:2026-05-21
标识
DOI:10.1182/blood.2026033577
摘要
The BCL-2 inhibitor venetoclax has shown promise in acute lymphoblastic leukemia (ALL), but its role in first-line therapy for newly diagnosed (ND) Philadelphia chromosome-negative (Ph⁻) ALL is undefined. In this prospective phase 2 study, 167 adolescents and adults (aged 14-60 years) with ND Ph⁻ ALL received venetoclax combined with pediatric-inspired chemotherapy. The primary endpoint was the rate of measurable residual disease (MRD) negativity by multiparameter flow cytometry (MFC) after induction. The complete remission rate was 91.0%, and 73.0% of responders achieved MFC-MRD negativity, meeting the primary endpoint. After a median follow-up of 19.3 months, median overall and disease-free survival were not reached; estimated 2-year survival rates were 78.5% and 76.7%, respectively. Propensity score-matched analysis confirmed superior survival compared with historical chemotherapy-only controls. Grade ≥ 3 adverse events were primarily hematologic toxicities and infections, with an incidence comparable to that of the historical cohort. These results demonstrate that adding venetoclax to pediatric-inspired chemotherapy significantly improves MRD response and survival outcomes in ND Ph⁻ ALL, with a manageable safety profile. This trial was registered with ClinicalTrials.gov under the identifier NCT05660473.
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