Fred Hutchinson Cancer Center, Seattle.
University of Washington, Seattle, Washington, USA.
AIDS. 2023 Jan 1;37(1):51-59. doi: 10.1097/QAD.0000000000003376. Epub 2022 Sep 2.
Improved understanding of the effect of HIV infection on Kaposi sarcoma (KS) presentation and outcomes will guide development of more effective KS staging and therapeutic approaches. We enrolled a prospective cohort of epidemic (HIV-positive; HIV + KS) and endemic (HIV-negative; HIV - KS) KS patients in Uganda to identify factors associated with survival and response.
Adults with newly diagnosed KS presenting for care at the Uganda Cancer Institute (UCI) in Kampala, Uganda, between October 2012 and December 2019 were evaluated. Participants received chemotherapy per standard guidelines and were followed over 1 year to assess overall survival (OS) and treatment response.
Two hundred participants were enrolled; 166 (83%) had HIV + KS, and 176 (88%) were poor-risk tumor (T1) stage. One-year OS was 64% (95% confidence interval [CI] 57-71%), with the hazard of death nearly threefold higher for HIV + KS (hazard ratio [HR] = 2.93; P = 0.023). Among HIV + KS, abnormal chest X-ray (HR = 2.81; P = 0.007), lower CD4 + T-cell count (HR = 0.68 per 100 cells/μl; P = 0.027), higher HIV viral load (HR = 2.22 per log 10 copies/ml; P = 0.026), and higher plasma Kaposi sarcoma-associated herpesvirus (KSHV) copy number (HR = 1.79 per log 10 copies/ml; P = 0.028) were associated with increased mortality. Among HIV - KS, factors associated with mortality included Karnofsky score <70 (HR = 9.17; P = 0.045), abnormal chest X-ray (HR = 8.41; P = 0.025), and higher plasma KSHV copy number (HR = 6.21 per log 10 copies/ml; P < 0.001).
Although survival rates were better for HIV - KS than HIV + KS, the high mortality rate seen in both groups underscores the urgent need to identify new staging and therapeutic approaches. Factors associated with mortality, including high plasma KSHV, may serve as important targets of therapy.
更好地了解 HIV 感染对卡波西肉瘤(KS)表现和结局的影响,将有助于制定更有效的 KS 分期和治疗方法。我们在乌干达招募了一个前瞻性队列的流行(HIV 阳性;HIV + KS)和地方性(HIV 阴性;HIV - KS)KS 患者,以确定与生存和反应相关的因素。
在 2012 年 10 月至 2019 年 12 月期间,在乌干达坎帕拉的乌干达癌症研究所(UCI)接受新诊断为 KS 的成年人接受了评估。参与者根据标准指南接受化疗,并在 1 年内进行随访,以评估总生存(OS)和治疗反应。
共纳入 200 名参与者;166 名(83%)为 HIV + KS,176 名(88%)为高危肿瘤(T1)期。1 年 OS 为 64%(95%置信区间[CI]57-71%),HIV + KS 死亡的风险几乎高出三倍(风险比[HR] = 2.93;P = 0.023)。在 HIV + KS 中,异常的胸部 X 线(HR = 2.81;P = 0.007)、较低的 CD4 + T 细胞计数(每 100 个细胞/μl 的 HR = 0.68;P = 0.027)、较高的 HIV 病毒载量(每 log10 拷贝/ml 的 HR = 2.22;P = 0.026)和较高的血浆卡波济肉瘤相关疱疹病毒(KSHV)拷贝数(每 log10 拷贝/ml 的 HR = 1.79;P = 0.028)与死亡率增加相关。在 HIV - KS 中,与死亡率相关的因素包括 Karnofsky 评分<70(HR = 9.17;P = 0.045)、异常的胸部 X 线(HR = 8.41;P = 0.025)和较高的血浆 KSHV 拷贝数(每 log10 拷贝/ml 的 HR = 6.21;P < 0.001)。
尽管 HIV - KS 的生存率好于 HIV + KS,但两组的高死亡率突出表明迫切需要确定新的分期和治疗方法。与死亡率相关的因素,包括高血浆 KSHV,可能是治疗的重要靶点。