Clinicopathological Features and Mortality in Patients With Kaposi Sarcoma and HIV: A Retrospective Analysis of a Thirty-Year Study From a Peruvian Oncologic Center

Author:

Cuellar Luis E.12ORCID,Meza Kelly34ORCID,Holguín Alexis Manuel1ORCID,Velarde Juan1ORCID,Portillo-Alvarez Diana1ORCID,Castro Victor1ORCID,Sulca-Huamani Oliver4,Intimayta-Escalante Claudio4ORCID,Gaby-Pérez Rushmely4ORCID,Patel Arpan5ORCID

Affiliation:

1. Instituto Nacional de Enfermedades Neoplasicas, Lima, Peru

2. Facultad de Medicina Hipólito Unanue, Universidad Nacional Federico Villarreal, Lima, Peru

3. Weill Cornell Medicine, New York, NY

4. Facultad de Medicina Humana, Universidad Nacional Mayor de San Marcos, Lima, Peru

5. Division of Hematology and Medical Oncology, Wilmot Cancer Institute, University of Rochester, Rochester, NY

Abstract

PURPOSE Kaposi's sarcoma (KS) is a multifocal angioproliferative disease. In Peru, the implementation of the highly active antiretroviral treatment (HAART) program was in 2005, the model for treating patients with HIV-positive KS shifted to a potential cure. In this study, we aim to compare clinicopathological characteristics and prognostic factors associated with outcomes in patients with HIV-positive KS. METHODS We developed a retrospective cohort study that includes patients with HIV/AIDS and KS seen in the Instituto Nacional de Enfermedades Neoplasicas between 1987 and 2017. Patients were divided into two groups according to the implementation of HAART in our country: the non-HAART group and those treated with HAART after 2005. Multivariate analysis for overall survival (OS) was performed with the Cox proportional hazard regression model. RESULTS There was a greater visceral compromise and more extensive oral cavity involvement in the non-HAART group (60% 31.7%, P < .01). Regarding the immune status, there was a significant difference from the CD4 count at 1-year follow-up (73 v 335, P = .01). The CD4/CD8 rate were significant different before QT (0.23 v 0.13, P = .01) and at 1-year follow-up (0.12 v 0.32, P = .03.). The estimated 5-year OS rate was significantly lower ( P = .0001) for the non-HAART group (41.7%; 95% CI, 25.9 to 56.9) compared with the HAART group (79.3%; 95% CI, 66.8 to 87.5). In the multivariate model for OS, full-HAART regimen and previous diagnosis of HIV/AIDS ( P < .01) were significantly associated with longer survival. CONCLUSION Clinical and demographic characteristics of our patients are compatible with the literature, but we report a higher rate of gastrointestinal involvement. Furthermore, our findings provide evidence for the importance of HAART and its ability to reduce KS-related mortality.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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