[The Comparison of Efficacy and Safety between Venetoclax Combined with Demethylating Drugs and the "3+7" Drug Regimen for Acute Myeloid Leukemia].

Q4 Medicine
Na Cui, Li-Jing Wang, Chang-Yong Yuan
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引用次数: 0

Abstract

Objective: To explore the efficacy and safety of venetoclax combined with demethylating drugs and intense chemotherapy in the treatment of acute myeloid leukemia (AML).

Methods: The clinical data of 76 patients with AML treated in Qilu Hospital of Shandong University Dezhou Hospital from January 2019 to March 2024 were retrospectively analyzed. Patients were divided into observation group and control group. 38 patients in the observation group received venetoclax combined with demethylating drugs (decitabine or azacytidine) and 38 patients in the control group with the "3+7" intensive chemotherapy regimen. The primary endpoints of clinical observation were complete remission (CR), CR with incomplete hematologic recovery (CRi), partial remission (PR), non remission (NR), and overall response rate (ORR). Secondary endpoints were overall survival (OS) and drug safety.

Results: After 2 courses of treatment, the CR+CRi rate in observation group and control group was 71.05% and 65.79%, respectively, and the ORR was 81.58% and 78.95%, respectively. After all courses of treatment, CR+CRi rate in the observation group and the control group was 73.68% and 78.95%, respectively, and the ORR was 81.58% and 84.21%, respectively, with no statistical significance between the two groups (P >0.05). After 1 course of treatment, there were statistically significant differences in the proportion and degree of myelosuppression, the duration of neutropenia and the duration of thrombocytopenia between the two groups (P < 0.05), while there were no statistically significant differences in the occurrence of neutropenia with fever between the two groups (P >0.05). The incidence of non-hematological adverse reactions was highest in infection (mainly pulmonary infection) and gastrointestinal reaction. Among the many adverse reactions, there were statistically significant differences in the infection and hypokalemia between the two groups (P < 0.05), the incidence of hypokalemia in observation group and control group was 42.11% and 15.79%, respectively, and the infection rate in observation group and control group was 73.68% and 94.74%, respectively. The median OS was 13.13(1.67-53.63) months in the observation group and 16.60(0.57-59.67) months in the control group.

Conclusion: The combination of venetoclax and demethylating drugs has a low degree of myelosuppression, but a long recovery time, a response rate as good as that of intensive chemotherapy, and a lower infection rate. However, the incidence of hypokalemia is low in the intensive chemotherapy regimen, and the regimen significantly improves the long-term outcome of patients.

【Venetoclax联合去甲基化药物与“3+7”方案治疗急性髓系白血病的疗效和安全性比较】。
目的:探讨维妥乐联合去甲基化药物及强化疗治疗急性髓性白血病(AML)的疗效和安全性。方法:回顾性分析2019年1月至2024年3月山东大学德州医院齐鲁医院收治的76例AML患者的临床资料。患者分为观察组和对照组。观察组38例患者采用venetoclax联合去甲基化药物(地西他滨或阿扎胞苷)治疗,对照组38例患者采用“3+7”强化化疗方案。临床观察的主要终点为完全缓解(CR)、CR伴不完全血液学恢复(CRi)、部分缓解(PR)、非缓解(NR)和总缓解率(ORR)。次要终点是总生存期(OS)和药物安全性。结果:2个疗程后,观察组和对照组的CR+CRi率分别为71.05%和65.79%,ORR分别为81.58%和78.95%。各疗程结束后,观察组与对照组CR+CRi率分别为73.68%、78.95%,ORR分别为81.58%、84.21%,两组比较差异无统计学意义(P < 0.05)。治疗1个疗程后,两组患者骨髓抑制比例、程度、中性粒细胞减少持续时间、血小板减少持续时间比较,差异均有统计学意义(P < 0.05),而中性粒细胞减少伴发热的发生率比较,差异均无统计学意义(P < 0.05)。非血液学不良反应发生率最高的是感染(主要是肺部感染)和胃肠道反应。在众多不良反应中,两组患者感染和低钾血症发生率差异有统计学意义(P < 0.05),观察组和对照组低钾血症发生率分别为42.11%和15.79%,观察组和对照组感染率分别为73.68%和94.74%。观察组中位OS为13.13(1.67 ~ 53.63)个月,对照组中位OS为16.60(0.57 ~ 59.67)个月。结论:venetoclax联合去甲基化药物治疗骨髓抑制程度低,但恢复时间长,有效率与强化化疗相当,且感染率较低。然而,在强化化疗方案中,低钾血症的发生率较低,并且该方案显著改善了患者的长期预后。
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来源期刊
中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
7331
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