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DOI 10.1080/14737140.2025.2474728

Медицинская библиотека · Expert review of anticancer therapy · 2025

Primary effusion lymphoma: therapeutic strategies targeting viral and cellular mechanisms.

Abou Staiteieh Soumaiah, Faddoul Nouria, Hayar Berthe, Houshaymi Bilal, Darwiche Nadine, Abou Merhi Raghida

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Аннотация

INTRODUCTION

Primary effusion lymphoma (PEL) is a rare subtype of B-cell lymphoma primarily affecting immunocompromised and elderly individuals. Given the dismal survival rates associated with traditional treatments, studying novel therapeutic approaches to improve patient outcomes is critical.

AREAS COVERED: This review focuses on developing therapeutic options for PEL that target particular viral and cellular mechanisms involved in PEL pathogenesis. Since the CHOP regimen was associated with a lower median survival rate, alternative treatments, including stem cell transplantation, have also been explored, but have generally produced unsatisfactory results. Therefore, novel therapeutic agents are under investigation, including antiretroviral drugs targeting viral pathways and treatments targeting particular cellular processes, such as DNA damage, epigenetics, apoptotic, and immune-modulatory pathways showing promising outcomes in preclinical and clinical research, increasing PEL treatment efficacy while minimizing toxicity. In this review, we conducted a comprehensive literature search using PubMed, and Google Scholar for studies published between 1989 and 2024.

EXPERT OPINION: Further research is needed to refine the appropriate combination methods and strategies behind drug interactions. Targeted therapies could be investigated further to improve therapeutic efficacy and reduce toxicity in this type of lymphoma.

Для цитирования: Abou Staiteieh Soumaiah, Faddoul Nouria, Hayar Berthe, Houshaymi Bilal, Darwiche Nadine, Abou Merhi Raghida. Primary effusion lymphoma: therapeutic strategies targeting viral and cellular mechanisms.. Expert review of anticancer therapy. 2025. DOI: 10.1080/14737140.2025.2474728.

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