State of the science and future directions for research on HIV and cancer: Summary of a joint workshop sponsored by IARC and NCI
- PMID: 37715370
- PMCID: PMC11133517
- DOI: 10.1002/ijc.34727
State of the science and future directions for research on HIV and cancer: Summary of a joint workshop sponsored by IARC and NCI
Abstract
An estimated 38 million people live with human immunodeficiency virus (HIV) worldwide and are at excess risk for multiple cancer types. Elevated cancer risks in people living with HIV (PLWH) are driven primarily by increased exposure to carcinogens, most notably oncogenic viruses acquired through shared transmission routes, plus acceleration of viral carcinogenesis by HIV-related immunosuppression. In the era of widespread antiretroviral therapy (ART), life expectancy of PLWH has increased, with cancer now a leading cause of co-morbidity and death. Furthermore, the types of cancers occurring among PLWH are shifting over time and vary in their relative burden in different parts of the world. In this context, the International Agency for Research on Cancer (IARC) and the US National Cancer Institute (NCI) convened a meeting in September 2022 of multinational and multidisciplinary experts to focus on cancer in PLWH. This report summarizes the proceedings, including a review of the state of the science of cancer descriptive epidemiology, etiology, molecular tumor characterization, primary and secondary prevention, treatment disparities and survival in PLWH around the world. A consensus of key research priorities and recommendations in these domains is also presented.
Keywords: cancer; epidemiology; human immunodeficiency virus; people living with HIV; prevention.
© 2023 International Agency for Research on Cancer; licensed by UICC and The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.
Conflict of interest statement
RVB reports support from the US National Institutes of Health, the Bill and Melinda Gates Foundation, and the World Health Organization. Regeneron Pharmaceuticals covered the cost of abstract and manuscript writing outside the submitted work. RVB serves on a Gilead Sciences DMC for which she receives an honorarium. KL reports research support from Bristol Myers Squibb and CTI BioPharma through CRADAs with the NCI and receiving drugs for clinical trials from Merck, EMD-Serono, and Eli Lilly. JMP reports financial support as Vir Biotechnologies- consultant; Virion Therapeutics- consultant; Antiva Biosciences- research grant support; Abbott- consultant; Roche Diagnostics-consultant; Vaccitech- research grant support. RR reports funding for clinical trials via Cooperative Research and Development Agreements (CRADA) between the institution and the following companies - BMS/Celgene, EMD-Serano, PDS Biotech, CTI Biopharma, Merck, and Lilly. GS reports grant funding from NIH/NCI. RY reports receiving research support from Celgene (now Bristol Myers Squibb) and CTI BioPharma through CRADAs with the NCI. RY also reports receiving drugs for clinical trials from Merck, EMD-Serano, and Eli Lill through CRADAs with the NCI, and he has received drug supply for laboratory research from Janssen Pharmaceuticals. RY is a co-inventor on US Patent 10,001,483 entitled “Methods for the treatment of Kaposi’s sarcoma or KSHV-induced lymphoma using immunomodulatory compounds and uses of biomarkers.” An immediate family member of RY is a co-inventor on patents or patent applications related to internalization of target receptors, epigenetic analysis, and ephrin tyrosine kinase inhibitors. All rights, title, and interest to these patents have been assigned to the U.S. Department of Health and Human Services; the government conveys a portion of the royalties it receives to its employee inventors under the Federal Technology Transfer Act of 1986 (P.L.99-502).
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