Nguyen Huong Q, Magaret Amalia S, Kitahata Mari M, Van Rompaey Stephen E, Wald Anna, Casper Corey
Department of Epidemiology, University of Washington, Seattle, Washington, USA.
AIDS. 2008 May 11;22(8):937-45. doi: 10.1097/QAD.0b013e3282ff6275.
To evaluate the role of highly active antiretroviral therapy and chemotherapy on tumor response among persons with AIDS-related Kaposi sarcoma and identify factors associated with response in a clinic setting.
Retrospective cohort.
One hundred and fourteen patients from two HIV clinics with a diagnosis of Kaposi sarcoma were identified via a clinical database. Records were reviewed to confirm Kaposi sarcoma diagnosis and abstract clinical and chemotherapy information. Demographics, laboratory values, and highly active antiretroviral therapy use were abstracted electronically. Cox's proportional hazards models identified predictors of Kaposi sarcoma improvement and resolution.
Thirty-six months following Kaposi sarcoma diagnosis, the rate of improvement among 64 patients with confirmed Kaposi sarcoma was 77% and that of complete resolution was 51%. In univariate analyses, recent chemotherapy was associated with Kaposi sarcoma improvement, and recent HIV viral load and highly active antiretroviral therapy were associated with both improvement and resolution. No measured baseline characteristics (tumor stage, diagnosis year, CD4 T-cell count, HIV viral load, or prior highly active antiretroviral therapy history) or recent CD4 T-cell counts predicted improvement or resolution. In multivariate analyses, recent chemotherapy (hazard ratio 5.5, 95% confidence interval: 2.7-11.2, P < 0.001) and highly active antiretroviral therapy (hazard ratio 4.1, 95% confidence interval: 1.4-12.6, P = 0.01) were predictors of improvement; only recent highly active antiretroviral therapy was associated with resolution (hazard ratio 6.2, 95% confidence interval: 1.5-26.4, P = 0.01). Response was not associated with type of highly active antiretroviral therapy regimen (non nucleoside reverse transcriptase inhibitor based, protease inhibitor based, or ritonavir-boosted protease inhibitor based).
Highly active antiretroviral therapy and chemotherapy are important in clinical Kaposi sarcoma response. Despite widespread availability of these therapies, Kaposi sarcoma continues to be a clinical problem; only half the patients achieved complete resolution of disease. New therapeutic approaches are needed.
评估高效抗逆转录病毒疗法和化疗在艾滋病相关卡波西肉瘤患者肿瘤反应中的作用,并确定临床环境中与反应相关的因素。
回顾性队列研究。
通过临床数据库识别出两家艾滋病毒诊所中114名诊断为卡波西肉瘤的患者。查阅记录以确认卡波西肉瘤诊断并提取临床和化疗信息。通过电子方式提取人口统计学、实验室值和高效抗逆转录病毒疗法的使用情况。Cox比例风险模型确定了卡波西肉瘤改善和消退的预测因素。
卡波西肉瘤诊断36个月后,64名确诊卡波西肉瘤患者的改善率为77%,完全消退率为51%。在单变量分析中,近期化疗与卡波西肉瘤改善相关,近期艾滋病毒病毒载量和高效抗逆转录病毒疗法与改善和消退均相关。没有测量的基线特征(肿瘤分期、诊断年份、CD4 T细胞计数、艾滋病毒病毒载量或既往高效抗逆转录病毒疗法史)或近期CD4 T细胞计数可预测改善或消退。在多变量分析中,近期化疗(风险比5.5,95%置信区间:2.7 - 11.2,P < 0.001)和高效抗逆转录病毒疗法(风险比4.1,95%置信区间:1.4 - 12.6,P = 0.01)是改善的预测因素;只有近期高效抗逆转录病毒疗法与消退相关(风险比6.2,95%置信区间:1.5 - 26.4,P = 0.01)。反应与高效抗逆转录病毒疗法方案类型(基于非核苷类逆转录酶抑制剂、基于蛋白酶抑制剂或基于利托那韦增强的蛋白酶抑制剂)无关。
高效抗逆转录病毒疗法和化疗对临床卡波西肉瘤反应很重要。尽管这些疗法广泛可得,但卡波西肉瘤仍然是一个临床问题;只有一半的患者实现了疾病的完全消退。需要新的治疗方法。