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Nanomedicine applications in lymphoma: advancing precision diagnostics, targeted therapeutics, and prospective developments
Department of Internal Medicine, Heme/Oncology Unit, University of Michigan, Ann Arbor, Michigan, USA; Department of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, Michigan, USA.ORCID iD: 0000-0001-5639-2208
Department of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, Michigan, USA; Department of Natural Sciences, College of Arts, Sciences, and Letters, University of Michigan, Dearborn, Michigan, USA.
Jamia Hamdard Medical College, Jamia Hamdard University, New Delhi, India.
Department of Neurology, Henry Ford Health, Detroit, Michigan, USA.
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2026 (English)In: VIEW, ISSN 2688-3988, article id 70180Article in journal (Refereed) Epub ahead of print
Abstract [en]

Lymphomas represent a biologically diverse group of B-, T-, and NK-cell malig-nancies, where challenges such as relapse, drug resistance, treatment-relatedtoxicity, sanctuary-site disease, and variable antigen expression continue toimpede therapeutic outcomes, despite significant advancements in immunother-apy. Nanomedicine presents a strategic approach to enhance drug delivery, targetmalignant lymphocytes or supportive microenvironmental cells, and integratemolecular imaging with therapy; however, the extent of clinical validation variesconsiderably across different platforms. This review provides an overview ofnanotechnology-enabled strategies for the treatment of lymphoma, includingantibody–drug and radioimmunoconjugates, liposomal and albumin-based drugcarriers, aptamer-guided systems, photothermal and photodynamic platforms,exosomes and liquid-biopsy nanoprobes, mRNA/lipid nanoparticle strategies,and AI-guided design. We highlight lymphoma-specific delivery challenges, suchas the presence of bulky nodal disease, circulating malignant cells, marrow andCNS involvement, splenic and hepatic sequestration, antigen sinks, and the lim-ited reliability of passive enhanced permeability and retention. Approved andguideline-supported examples are differentiated from active clinical trials and preclinical-only concepts to provide a clinically oriented interpretation of thecurrent evidence and future translational priorities.

Place, publisher, year, edition, pages
Australia: John Wiley & Sons, 2026. article id 70180
Keywords [en]
B‑cell markers, CAR‑T, diagnostics, gene therapy, immunotherapy, lymphoma, nanocarrierdesign, nanomedicine, phototherapy, targeted drug delivery
National Category
Cancer and Oncology
Research subject
nanoparticles
Identifiers
URN: urn:nbn:se:umu:diva-256935DOI: 10.1002/viw2.70180ISI: 001822040700001Scopus ID: 2-s2.0-105045128367OAI: oai:DiVA.org:umu-256935DiVA, id: diva2:2088796
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Cancer cachexia
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Cancerforskningsfonden i Norrland, AMP 25-1203Available from: 2026-07-29 Created: 2026-07-29 Last updated: 2026-07-30

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Shah, Farhan Khalid

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Rauf, Mohd AhmarIyer, Arun K.Shah, Farhan Khalid
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