A prospective cohort study identifies two types of HIV+ Kaposi Sarcoma lesions: proliferative and inflammatory

Author:

Moorad Razia12,Kasonkanji Edwards3,Gumulira Joe4,Gondwe Yolanda3ORCID,Dewey Morgan3,Pan Yue15,Peng Alice1,Pluta Linda J.1,Kudowa Evaristar2,Nyasosela Richard6,Tomoka Tamiwe3,Tweya Hannock4,Heller Tom4,Gugsa Salem4,Phiri Sam4,Moore Dominic T.1,Damania Blossom127,Painschab Matthew13,Hosseinipour Mina C.137,Dittmer Dirk P.127ORCID

Affiliation:

1. Lineberger Comprehensive Cancer Center, School of Medicine University of North Carolina at Chapel Hill Chapel Hill North Carolina USA

2. Department of Immunology and Microbiology University of North Carolina at Chapel Hill Chapel Hill North Carolina USA

3. UNC Project Malawi Lilongwe Malawi

4. Lighthouse Trust Lilongwe Malawi

5. Department of Biostatistics The University of North Carolina at Chapel Hill Chapel Hill North Carolina USA

6. Kamuzu Central Hospital Lilongwe Malawi

7. Institute for Global Health and Infectious Diseases University of North Carolina at Chapel Hill Chapel Hill North Carolina USA

Abstract

AbstractKaposi sarcoma (KS) is the most common cancer in people living with HIV (PLWH) in many countries where KS‐associated herpesvirus is endemic. Treatment has changed little in 20 years, but the disease presentation has. This prospective cohort study enrolled 122 human immunodeficiency virus (HIV) positive KS patients between 2017 and 2019 in Malawi. Participants were treated with bleomycin, vincristine and combination antiretroviral therapy, the local standard of care. One‐year overall survival was 61%, and progression‐free survival was 58%. The 48‐week complete response rate was 35%. RNAseq (n = 78) differentiated two types of KS lesions, those with marked endothelial characteristics and those enriched in inflammatory transcripts. This suggests that different KS lesions are in different disease states consistent with the known heterogeneous clinical response to treatment. In contrast to earlier cohorts, the plasma HIV viral load of KS patients in our study was highly variable. A total of 25% of participants had no detectable HIV; all had detectable KSHV viral load. Our study affirms that many KS cases today develop in PLWH with well‐controlled HIV infection and that different KS lesions have differing molecular compositions. Further studies are needed to develop predictive biomarkers for this disease.

Funder

U.S. Public Health Service

Publisher

Wiley

Subject

Cancer Research,Oncology

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