Venetoclax plus daunorubicin and cytarabine in newly diagnosed acute myeloid leukemia patients: A propensity score-matched analysis

IF 3.3 4区 医学 Q2 HEMATOLOGY Hematological Oncology Pub Date : 2024-02-28 DOI:10.1002/hon.3260
Rong Wang, Yi Zhang, Jie Chang, Huafeng Wang, Yinjun Lou, Min Yang, Gaixiang Xu, Hongyan Tong, Wanzhuo Xie, De Zhou, Juying Wei, Wenyuan Mai, Xiujin Ye, Haitao Meng, Jie Jin, Hong-Hu Zhu
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Abstract

Venetoclax plus 3 + 7 daunorubicin and cytarabine chemotherapy (DAV) has shown safety and efficacy in eligible patients with newly diagnosed acute myeloid leukemia (AML). However, there are no direct comparisons between DAV and 3 + 7 daunorubicin and cytarabine chemotherapy (DA) alone. We performed a propensity score-matched analysis to compare the outcomes of DAV group with historical DA group and identify the clinical and molecular characteristics of patients who might benefit from the DAV regimen. The DAV group had a higher Complete remission (CR) rate than the DA group (90% vs. 55%, p = 0.008). 25 (96%) patients in the DAV group had a higher MRD-negative CRc rate compared with 13 (62%) patients in the DA group (p = 0.006). After a median follow-up duration of 19.15 (IQR 17.13–21.67) months, the DAV group had an improved overall survival (p = 0.001) and event-free survival (p = 0.069), but not disease-free survival (p = 0.136). Collectively, DAV regimen induced high CR rates and deep MRD-negative CRc rates after one cycle of induction therapy, as well as prolonged the overall survival, in young adult patients with AML who were eligible for intensive chemotherapy. The addition of venetoclax to intensive chemotherapy should be considered in the future to achieve better survival advantages in eligible AML patients.

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Venetoclax 加多柔比星和阿糖胞苷治疗新诊断的急性髓性白血病患者:倾向得分匹配分析
Venetoclax 加 3+7 达诺罗比星和阿糖胞苷化疗(DAV)已在符合条件的新诊断急性髓性白血病(AML)患者中显示出安全性和有效性。然而,目前还没有将 DAV 与 3 + 7 达诺鲁比星和阿糖胞苷化疗(DA)进行直接比较。我们进行了倾向得分匹配分析,比较了DAV组与历史DA组的疗效,并确定了可能从DAV方案中获益的患者的临床和分子特征。DAV组的完全缓解率(CR)高于DA组(90%对55%,P = 0.008)。DAV组25名患者(96%)的MRD阴性CRc率高于DA组13名患者(62%)(P = 0.006)。中位随访时间为 19.15(IQR 17.13-21.67)个月后,DAV 组的总生存期(p = 0.001)和无事件生存期(p = 0.069)有所改善,但无病生存期(p = 0.136)没有改善。总之,对于符合强化化疗条件的年轻成人急性髓细胞白血病患者,DAV方案在一个周期的诱导治疗后可诱导出较高的CR率和较深的MRD阴性CRc率,并延长了总生存期。未来应考虑在强化化疗中加入venetoclax,以提高符合条件的急性髓细胞白血病患者的生存率。
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来源期刊
Hematological Oncology
Hematological Oncology 医学-血液学
CiteScore
4.20
自引率
6.10%
发文量
147
审稿时长
>12 weeks
期刊介绍: Hematological Oncology considers for publication articles dealing with experimental and clinical aspects of neoplastic diseases of the hemopoietic and lymphoid systems and relevant related matters. Translational studies applying basic science to clinical issues are particularly welcomed. Manuscripts dealing with the following areas are encouraged: -Clinical practice and management of hematological neoplasia, including: acute and chronic leukemias, malignant lymphomas, myeloproliferative disorders -Diagnostic investigations, including imaging and laboratory assays -Epidemiology, pathology and pathobiology of hematological neoplasia of hematological diseases -Therapeutic issues including Phase 1, 2 or 3 trials as well as allogeneic and autologous stem cell transplantation studies -Aspects of the cell biology, molecular biology, molecular genetics and cytogenetics of normal or diseased hematopoeisis and lymphopoiesis, including stem cells and cytokines and other regulatory systems. Concise, topical review material is welcomed, especially if it makes new concepts and ideas accessible to a wider community. Proposals for review material may be discussed with the Editor-in-Chief. Collections of case material and case reports will be considered only if they have broader scientific or clinical relevance.
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