Effect of Two Different ART Regimens on AIDS Patients With Lymphoma

IF 2 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Guangjing Ruan, Qisi Su, Zhiman Xie, Huawei He, Yuming Lu, Ningmei Liu, Dandan Ni, Bin He
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引用次数: 0

Abstract

Objective: To explore the impact of two different ART regimens on AIDS patients with lymphoma.

Methods: A retrospective study was carried out involving 60 patients diagnosed with AIDS and lymphoma and treated in our hospital during the period from June 2022 to December 2023. All patients underwent DA-EPOCH chemotherapy. According to the differences in ART treatment regimens, patients receiving the DTG + lamivudine (3TC) regimen will be categorized into the DTG + 3TC group, and patients receiving the TDF + 3TC + efavirenz (EFV) regimen will be classified into the TDF + 3TC + EFV group, with 30 cases in each group. The HIV viral load was compared between the two groups pretreatment and posttreatment (at 12, 24, and 26 weeks). The immunological indices (CD4+ and CD8+), liver function indices (serum total bilirubin [TBIL], alanine transaminase [ALT], aspartate transaminase [AST], serum albumin [ALB], and prothrombin time [PT]), and blood creatinine (Scr) levels of the two groups were compared before and after treatment (at 36 weeks). The occurrence of adverse reactions was documented.

Results: After 12, 24, and 36 weeks of treatment, the HIV viral load in the DTG + 3TC group was consistently lower than that in the EFV + TDF + 3TC group (p < 0.05). At week 36 posttreatment, compared with the EFV + TDF + 3TC group, the DTG + 3TC group showed higher CD4+ counts and lower CD8+ counts (p < 0.05). Following treatment at week 36, levels of AST, ALT, TBiL, and PT were elevated in both groups but lower in the DTG + 3TC group (p < 0.05). The levels of ALB in both groups were decreased, but the DTG + 3TC group was significantly higher (p < 0.05). Additionally, at week 36 posttreatment, Scr levels were significantly better in the DTG + 3TC group compared to the EFV + TDF + 3TC group (p < 0.05). The incidence of adverse reactions in the DTG + 3TC group and EFV + TDF + 3TC group differed significantly, with rates of 13.33% and 23.33%, respectively (p > 0.05).

Conclusion: There is no difference in the safety of DTG + 3TC in the treatment of AIDS patients with ARL compared with TDF +3TC + EFV. However, the combination of DTG + 3TC simplified regimen is superior to the three-drug regimen of TDF + 3TC + EFV in reducing viral load and has positive effects on the improvement of liver function and blood creatinine, with no obvious side effects.

Abstract Image

两种不同抗逆转录病毒治疗方案对艾滋病淋巴瘤患者的影响
目的:探讨两种不同抗逆转录病毒治疗方案对艾滋病淋巴瘤患者的影响。方法:对2022年6月至2023年12月在我院治疗的60例艾滋病淋巴瘤患者进行回顾性研究。所有患者均接受DA-EPOCH化疗。根据ART治疗方案的差异,将接受DTG +拉米夫定(3TC)方案的患者分为DTG + 3TC组,接受TDF + 3TC +依非韦伦(EFV)方案的患者分为TDF + 3TC + EFV组,每组30例。比较两组治疗前和治疗后(12、24和26周)的HIV病毒载量。比较两组患者治疗前后(36周)免疫指标(CD4+、CD8+)、肝功能指标(血清总胆红素(TBIL)、丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、血清白蛋白(ALB)、凝血酶原时间(PT))及血肌酐(Scr)水平。记录不良反应的发生情况。结果:治疗12、24、36周后,DTG + 3TC组的HIV病毒载量均低于EFV + TDF + 3TC组(p < 0.05)。治疗后第36周,与EFV + TDF + 3TC组比较,DTG + 3TC组CD4+计数较高,CD8+计数较低(p < 0.05)。治疗第36周后,两组患者AST、ALT、TBiL、PT水平均升高,DTG + 3TC组降低(p < 0.05)。两组ALB水平均降低,但DTG + 3TC组ALB水平显著升高(p < 0.05)。此外,在治疗后第36周,DTG + 3TC组的Scr水平显著高于EFV + TDF + 3TC组(p < 0.05)。DTG + 3TC组和EFV + TDF + 3TC组不良反应发生率差异有统计学意义,分别为13.33%和23.33% (p > 0.05)。结论:与TDF +3TC + EFV相比,DTG +3TC治疗艾滋病ARL患者的安全性无显著差异。但DTG + 3TC简化联合方案在降低病毒载量方面优于TDF + 3TC + EFV三药方案,对肝功能和血肌酐的改善均有积极作用,且无明显副作用。
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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
226
审稿时长
6 months
期刊介绍: The Journal of Clinical Pharmacy and Therapeutics provides a forum for clinicians, pharmacists and pharmacologists to explore and report on issues of common interest. Reports and commentaries on current issues in medical and pharmaceutical practice are encouraged. Papers on evidence-based clinical practice and multidisciplinary collaborative work are particularly welcome. Regular sections in the journal include: editorials, commentaries, reviews (including systematic overviews and meta-analyses), original research and reports, and book reviews. Its scope embraces all aspects of clinical drug development and therapeutics, including: Rational therapeutics Evidence-based practice Safety, cost-effectiveness and clinical efficacy of drugs Drug interactions Clinical impact of drug formulations Pharmacogenetics Personalised, stratified and translational medicine Clinical pharmacokinetics.
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