Medical Research Council, Clinical Trials Unit, 222 Euston Rd, London NW1 2DA, UK.
J Natl Cancer Inst. 2010 Jun 2;102(11):784-92. doi: 10.1093/jnci/djq134. Epub 2010 May 4.
Despite the success of combination antiretroviral therapy (cART) in reducing the incidence of Kaposi sarcoma, HIV-infected individuals who have responded to treatment continue to be diagnosed with Kaposi sarcoma. We examine factors associated with the incidence of Kaposi sarcoma among cART-treated HIV-infected homosexual men and changes in their survival after its diagnosis over calendar time.
Data were from HIV-infected homosexual men with well-estimated dates of HIV seroconversion (ie, change in status from being HIV negative to having HIV antibodies detected). Incidence of Kaposi sarcoma was calculated. We used Kaplan-Meier methods to determine survival after Kaposi sarcoma diagnosis in three calendar periods: before 1996, 1996-2000, and 2001-2006. Poisson models were used to examine the effect of risk factors such as current and nadir CD4 cell count (ie, the lowest CD4 cell count ever recorded for a person), duration of infection, and age at diagnosis for Kaposi sarcoma incidence in cART-treated men. All statistical tests were two-sided.
Among the 9473 men, 555 were diagnosed with Kaposi sarcoma in the period 1986-2006, of whom 319 died. The percentage surviving 24 months after Kaposi sarcoma diagnosis rose statistically significantly during the study period from 35% (95% confidence interval [CI] = 29% to 42%) before 1996 to 84% (95% CI = 76% to 90%) in 1996-2000 and to 81% (95% CI = 70% to 88%) in 2001-2006 (P < .001). Seventy men were diagnosed with Kaposi sarcoma after starting cART. Current (ie, within 6 months) CD4 cell count was associated with incidence of Kaposi sarcoma among cART-treated men (rate ratios [RRs] = 18.91, 95% CI = 8.50 to 42.09, for CD4 level category <200 cells per cubic millimeter; RR = 3.55, 95% CI = 1.40 to 9.00, for 200-349 cells per cubic millimeter; and RR = 4.11, 95% CI = 1.74 to 9.70, for 350-499 cells per cubic millimeter; all compared with > or = 500 cells per cubic millimeter). After adjustment for current CD4 cell count, HIV infection duration, age, or nadir CD4 cell count was not associated with Kaposi sarcoma incidence.
Among cART-treated HIV-infected homosexual men, current CD4 cell count was the factor most strongly associated with the incidence of Kaposi sarcoma. Survival estimates after Kaposi sarcoma diagnosis have improved over time.
尽管联合抗逆转录病毒疗法(cART)在降低卡波西肉瘤的发病率方面取得了成功,但对治疗有反应的 HIV 感染者仍会被诊断出患有卡波西肉瘤。我们研究了与接受 cART 治疗的 HIV 感染同性恋男性中卡波西肉瘤发病率相关的因素,以及在日历时间内该病诊断后患者生存率的变化。
数据来自于 HIV 感染的同性恋男性,这些男性的 HIV 血清转换日期(即从 HIV 阴性转为 HIV 抗体检测阳性的时间)估计较为准确。计算卡波西肉瘤的发病率。我们使用 Kaplan-Meier 方法来确定在三个日历时期(1996 年之前、1996-2000 年和 2001-2006 年)中,卡波西肉瘤诊断后患者的生存情况。我们使用泊松模型来检验当前和最低 CD4 细胞计数(即个体有记录以来的最低 CD4 细胞计数)、感染持续时间和诊断时年龄等危险因素对接受 cART 治疗的男性中卡波西肉瘤发病率的影响。所有的统计检验均为双侧检验。
在 9473 名男性中,有 555 人在 1986-2006 年间被诊断患有卡波西肉瘤,其中 319 人死亡。Kaposi 肉瘤诊断后 24 个月的存活率在研究期间呈统计学显著上升,从 1996 年之前的 35%(95%置信区间[CI]为 29%至 42%)上升到 1996-2000 年的 84%(95%CI为 76%至 90%),再上升到 2001-2006 年的 81%(95%CI 为 70%至 88%)(P<.001)。70 名男性在开始接受 cART 后被诊断患有卡波西肉瘤。当前(即 6 个月内)CD4 细胞计数与接受 cART 治疗的男性的卡波西肉瘤发病率相关(发病率比[RR]为 18.91,95%CI 为 8.50 至 42.09,CD4 水平<200 个细胞/立方毫米;RR=3.55,95%CI 为 1.40 至 9.00,CD4 水平为 200-349 个细胞/立方毫米;RR=4.11,95%CI 为 1.74 至 9.70,CD4 水平为 350-499 个细胞/立方毫米;与 CD4 水平>或=500 个细胞/立方毫米相比)。在调整当前 CD4 细胞计数后,HIV 感染持续时间、年龄或最低 CD4 细胞计数与卡波西肉瘤发病率无关。
在接受 cART 治疗的 HIV 感染同性恋男性中,当前 CD4 细胞计数是与卡波西肉瘤发病率最密切相关的因素。卡波西肉瘤诊断后,估计生存率随着时间的推移而提高。