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在基于蛋白酶抑制剂的抗逆转录病毒治疗转换后,HIV-1 得到控制的患者中,卡波西肉瘤复发的风险没有增加。

No increased risk of Kaposi sarcoma relapse in patients with controlled HIV-1 infection after switching protease inhibitor-based antiretroviral therapy.

机构信息

Department of Infectious and Tropical Diseases, Toulouse University Hospital, Toulouse, France.

Department of Infectious and Tropical Diseases, Martinique University Hospital, Fort de France, FWI and INSERM UMR 1027 Toulouse III University, Toulouse, France.

出版信息

HIV Med. 2022 Mar;23(3):301-306. doi: 10.1111/hiv.13168. Epub 2021 Oct 19.

Abstract

OBJECTIVES

Our aim was to assess if switching from a protease inhibitors (PI)-based regimen to a PI-free one is associated with an increased risk of Kaposi Sarcoma (KS) relapse among patients living with HIV (PLHIV) with history of KS and controlled HIV replication.

METHODS

In a retrospective analysis of the prospectively collected Dat'AIDS database we selected patients who both had a past KS history and a HIV-1 viral load below 200 copies/mL while being PI-treated. We searched for KS relapses while persistent virological success was maintained for at least 6 months, whether patients kept taking the PI, or switched to PI-free regimen.

RESULTS

Among the 216 patients with past KS event and a history of HIV-1 infection efficiently treated by a PI-based regimen, 148 patients (68.5%) later switched to a PI-sparing regimen. Their baseline characteristics were not different from non-switching patients. We described 7 cases of relapse (3.2% of the 216 patients). Five cases of relapse occurred in switching patients (3.4%). The remaining two relapses occurred in PI-treated patients (2.9%). At KS relapse, CD4 cell count was 459 cells/μL (range 225-560) for switching patients, compared with 362 and 136 cells/μL for the other two patients.

CONCLUSIONS

In this large cohort of PLHIV with a history of KS and ART-controlled HIV replication, KS relapses were described in 3.2% of the patients, and were not more frequent when a PI-containing ART regimen has been switched to a PI-free regimen. Our results do not support a specific effect of PI on KS.

摘要

目的

我们旨在评估对于有卡波西肉瘤(KS)病史且 HIV 复制得到控制的 HIV 感染者(PLHIV),从基于蛋白酶抑制剂(PI)的方案转换为无 PI 方案是否会增加 KS 复发的风险。

方法

在对前瞻性收集的 Dat'AIDS 数据库进行的回顾性分析中,我们选择了那些既有 KS 病史又有 HIV-1 病毒载量低于 200 拷贝/mL 且正在接受 PI 治疗的患者。我们寻找了在持续病毒学成功至少 6 个月的情况下发生的 KS 复发,无论患者是否继续服用 PI 还是转换为无 PI 方案。

结果

在 216 名有过去 KS 事件和 HIV-1 感染病史且接受 PI 方案有效治疗的患者中,有 148 名患者(68.5%)后来转换为 PI 节约方案。他们的基线特征与未转换患者无差异。我们描述了 7 例复发(216 名患者中的 3.2%)。5 例复发发生在转换患者中(3.4%)。其余 2 例复发发生在接受 PI 治疗的患者中(2.9%)。在 KS 复发时,转换患者的 CD4 细胞计数为 459 个/μL(范围 225-560),而其他两名患者的 CD4 细胞计数分别为 362 和 136 个/μL。

结论

在这个有 KS 病史和 ART 控制的 HIV 复制的大型 PLHIV 队列中,有 3.2%的患者出现了 KS 复发,而当含有 PI 的 ART 方案转换为无 PI 方案时,复发并不更频繁。我们的结果不支持 PI 对 KS 有特定的作用。

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