Immune-checkpoint blockade and candidate predictive biomarkers in HIV-negative Kaposi sarcoma: current evidence and a practical research framework
- 1Department of Oncology, Sichuan Academy of Medical Sciences and Sichuan Provincial People’s Hospital
- 2School of Medicine, University of Electronic Science and Technology of China
Abstract
Kaposi sarcoma (KS) is a KSHV/HHV-8-driven vascular neoplasm with heterogeneous HIV-negative epidemiological settings. Immune-checkpoint blockade is biologically plausible, but direct clinical evidence remains limited to a small, non-comparative phase II cohort of pembrolizumab in classic or endemic KS. Its 71% best objective response rate is a signal that warrants confirmation, not comparative evidence or a basis for biomarker-guided treatment. This narrative review distinguishes established clinical observations from candidate translational hypotheses, appraises analytical and biological limitations of proposed markers, and outlines requirements for prospective subtype-stratified validation. PD-L1 expression, tumor mutational burden, and KSHV DNA should not be used as stand-alone selection or exclusion tests in routine care.
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BibTeX
@article{song2026immunecheckpoint,
title = {{Immune-checkpoint blockade and candidate predictive biomarkers in HIV-negative Kaposi sarcoma: current evidence and a practical research framework}},
author = {Yang Song and Yan Fang and Lin Zeng and Hua Guan},
journal = {Frontiers in Immunology},
year = {2026},
month = oct,
doi = {10.3389/fimmu.2026.1979969},
url = {https://www.frontiersin.org/articles/10.3389/fimmu.2026.1979969/full},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Immune-checkpoint blockade and candidate predictive biomarkers in HIV-negative Kaposi sarcoma: current evidence and a practical research framework
AU - Yang Song
AU - Yan Fang
AU - Lin Zeng
AU - Hua Guan
PY - 2026
DA - 2026/10/16
JO - Frontiers in Immunology
DO - 10.3389/fimmu.2026.1979969
UR - https://www.frontiersin.org/articles/10.3389/fimmu.2026.1979969/full
AB - Kaposi sarcoma (KS) is a KSHV/HHV-8-driven vascular neoplasm with heterogeneous HIV-negative epidemiological settings. Immune-checkpoint blockade is biologically plausible, but direct clinical evidence remains limited to a small, non-comparative phase II cohort of pembrolizumab in classic or endemic KS. Its 71% best objective response rate is a signal that warrants confirmation, not comparative evidence or a basis for biomarker-guided treatment. This narrative review distinguishes established clinical observations from candidate translational hypotheses, appraises analytical and biological limitations of proposed markers, and outlines requirements for prospective subtype-stratified validation. PD-L1 expression, tumor mutational burden, and KSHV DNA should not be used as stand-alone selection or exclusion tests in routine care.
SN - 1664-3224
ER -