[地西他滨联合预激方案治疗对初始标准诱导化疗无反应的新诊断急性髓细胞白血病患者的疗效]。

Li-Min Hou, Ying Gao, Qiu-Ying Gao, Ben Niu
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Fifty-one patients who accepted pre-excitation regimen were divided into regular group, while another 51 patients treated with decitabine combined with pre-excitation regimen were divided into combination group. The efficacy, incidence of toxic and side effects, Core Scale of Quality of Life (QLQ-C30) score before and after treatment, T lymphocyte subsets (CD3<sup>+</sup>, CD4<sup>+</sup>, CD4<sup>+</sup>/CD8<sup>+</sup>, Tregs) and 3-year overall survival (OS) rate were compared between the two groups.</p><p><strong>Results: </strong>The total effective rate of combination group was 80.39%, which was significantly higher than 62.75% of regular group (<i>P</i> < 0.05). After treatment, the QLQ-C30 score of combination group was 60.27±6.96, which was significantly lower than 65.73±7.96 of regular group (<i>P</i> < 0.001). There was no statistical difference in the incidence of toxic and side effects between the two groups (<i>P</i> >0.05). 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引用次数: 0

摘要

目的探讨地西他滨联合预激方案治疗首次标准诱导化疗未缓解的新诊断急性髓性白血病(AML)患者的疗效及其对调节性T淋巴细胞(Tregs)相对含量的影响:回顾性分析2013年3月至2019年3月陕西省人民医院收治的102例经首次标准诱导化疗未缓解的新诊断AML患者(急性早幼粒细胞白血病除外)的临床资料。将接受预激方案治疗的51例患者分为常规组,将地西他滨联合预激方案治疗的51例患者分为联合组。比较两组患者的疗效、毒副反应发生率、治疗前后生活质量核心量表(QLQ-C30)评分、T淋巴细胞亚群(CD3+、CD4+、CD4+/CD8+、Tregs)和3年总生存率(OS):联合组总有效率为80.39%,明显高于常规组的62.75%(P<0.05)。治疗后,联合组的 QLQ-C30 评分为(60.27±6.96)分,明显低于常规组的(65.73±7.96)分(P<0.001)。两组毒副反应发生率无统计学差异(P>0.05)。治疗后,联合组的CD3+、CD4+、CD4+/CD8+水平高于常规组(均P<0.001),而Treg水平低于常规组(P<0.001)。联合组的3年OS率为72.55%,明显高于常规组的52.94%(P < 0.001):结论:地西他滨联合预激方案对第一疗程标准诱导化疗疗效不佳的急性髓细胞白血病患者有显著疗效。结论:地西他滨联合预激方案对第一疗程标准诱导化疗效果不明显的急性髓细胞白血病患者有明显疗效,可通过调节Tregs的相对含量,减轻抗肿瘤免疫抑制,改善免疫功能,从而延长患者生存时间,提高生活质量,且不会增加不良反应。
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[Efficacy of Decitabine Combined with Preexcitation Regimen in Treatment of Newly Diagnosed AML Patients Who Did not Respond to Initial Standard Induction Chemotherapy].

Objective: To investigate the efficacy of decitabine combined with preexcitation regimen in the treatment of newly diagnosed acute myeloid leukemia (AML) patients who have not been relieved by the first standard induction chemotherapy and its influence on the relative content of regulatory T lymphocytes (Tregs).

Methods: The clinical data of 102 newly diagnosed AML patients (except acute promyelocytic leukemia) who did not relieve after initial standard induction chemotherapy in Shaanxi Provincial People's Hospital from March 2013 to March 2019 were retrospectively analyzed. Fifty-one patients who accepted pre-excitation regimen were divided into regular group, while another 51 patients treated with decitabine combined with pre-excitation regimen were divided into combination group. The efficacy, incidence of toxic and side effects, Core Scale of Quality of Life (QLQ-C30) score before and after treatment, T lymphocyte subsets (CD3+, CD4+, CD4+/CD8+, Tregs) and 3-year overall survival (OS) rate were compared between the two groups.

Results: The total effective rate of combination group was 80.39%, which was significantly higher than 62.75% of regular group (P < 0.05). After treatment, the QLQ-C30 score of combination group was 60.27±6.96, which was significantly lower than 65.73±7.96 of regular group (P < 0.001). There was no statistical difference in the incidence of toxic and side effects between the two groups (P >0.05). After treatment, the levels of CD3+, CD4+, CD4+/CD8+ in the combination group were higher than those in the regular group (all P < 0.001), while Treg was lower (P < 0.001). The 3-year OS rate in the combination group was 72.55%, which was significantly higher than 52.94% in the regular group (P < 0.001).

Conclusion: Decitabine combined with preexcitation regimen has a significant effect on AML patients who have not been alleviated by standard induction chemotherapy in the first course of treatment. It can reduce anti-tumor immune suppression and improve immune function by regulating the relative content of Tregs, thus prolongs survival time and improves life quality of patients without increasing adverse reactions.

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中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
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7331
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