Evaluation of a Predictive Staging Model for HIV-Associated Kaposi Sarcoma in Uganda. (15th April 2017)

• Record Type: Journal Article
• Authors: Okuku, Fred; Krantz, Elizabeth M.; Kafeero, James; Kamya, Moses R.; Orem, Jackson; Casper, Corey; Phipps, Warren
• Is Part Of: Journal of acquired immune deficiency syndromes. Volume 74:Number 5(2017)
• Publication Date: 2017-04-15
• Subjects: Kaposi sarcoma -- staging -- sub-Saharan Africa; AIDS (Disease) -- Periodicals; Acquired Immunodeficiency Syndrome -- Periodicals; AIDS (Disease); Periodicals; 616.9792005
• DOI: 10.1097/QAI.0000000000001286
• Languages: English
• ISSNs: 1525-4135

Abstract

Abstract : Background: HIV-associated Kaposi sarcoma (KS) is commonly staged using the AIDS Clinical Trials Group criteria, which classify 3 variables— tumor extent (T), immune status (I), and systemic symptoms (S)—into good risk (0) and poor risk (1). Although validated in the United States and Europe, these criteria have not been systematically evaluated in sub-Saharan Africa, where the burden of KS is greatest. Methods: We reviewed medical charts of adult patients with HIV-associated KS seen at the Uganda Cancer Institute from 1992 to 2007. Vital status at 2 years after KS diagnosis was determined from the medical chart, or by contacting the patient or next of kin. Survival estimates used Kaplan–Meier methods. Predictors were evaluated for 2 periods: 0–4 months and 4–24 months after diagnosis. Results: At 2 years after diagnosis, 167 (41%) patients were alive, 156 (39%) had died, and 81 (20%) were lost to follow-up. The Kaplan–Meier estimate of 2-year survival was 57%. S1 was associated with death in months 0–4 [hazard ratio: 6.4, 95% confidence interval: 1.9–21.1], whereas T1 was associated with death in months 4–24 [hazard ratio: 4.0, 95% confidence interval: 1.4 to 11.5]. Immune status was not associated with survival. Conclusions: Systemic symptoms were strongly associated with death in the early period after KS diagnosis, whereas tumor status was most predictive of death in the 4- to 24-month period. These findings suggest that different processes may influence outcomes in early and late periods following KS diagnosis. Further studies are needed to confirm these observations and to identify better predictors of KS survival in sub-Saharan Africa. Abstract : Supplemental Digital Content is Available in the Text.