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dc.contributor.authorvan der Meel, Roy
dc.contributor.authorSulheim, Einar
dc.contributor.authorShi, Yang
dc.contributor.authorKiessling, Fabian
dc.contributor.authorMulder, Willem J.M.
dc.contributor.authorLammers, Twan
dc.date.accessioned2021-03-19T12:19:07Z
dc.date.available2021-03-19T12:19:07Z
dc.date.created2019-11-22T10:48:59Z
dc.date.issued2019
dc.identifier.citationNature Nanotechnology. 2019, 14 (11), 1007-1017.en_US
dc.identifier.issn1748-3387
dc.identifier.urihttps://hdl.handle.net/11250/2734489
dc.description.abstractNanomedicines are extensively employed in cancer therapy. We here propose four strategic directions to improve nanomedicine translation and exploitation. (1) Patient stratification has become common practice in oncology drug development. Accordingly, probes and protocols for patient stratification are urgently needed in cancer nanomedicine, to identify individuals suitable for inclusion in clinical trials. (2) Rational drug selection is crucial for clinical and commercial success. Opportunistic choices based on drug availability should be replaced by investments in modular (pro)drug and nanocarrier design. (3) Combination therapies are the mainstay of clinical cancer care. Nanomedicines synergize with pharmacological and physical co-treatments, and should be increasingly integrated in multimodal combination therapy regimens. (4) Immunotherapy is revolutionizing the treatment of cancer. Nanomedicines can modulate the behaviour of myeloid and lymphoid cells, thereby empowering anticancer immunity and immunotherapy efficacy. Alone and especially together, these four directions will fuel and foster the development of successful cancer nanomedicine therapies.en_US
dc.language.isoengen_US
dc.publisherNature Researchen_US
dc.titleSmart cancer nanomedicineen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionsubmittedVersionen_US
dc.source.pagenumber1007-1017en_US
dc.source.volume14en_US
dc.source.journalNature Nanotechnologyen_US
dc.source.issue11en_US
dc.identifier.doi10.1038/s41565-019-0567-y
dc.identifier.cristin1750865
dc.description.localcodeThis article will not be available due to copyright restrictions © 2019 by Nature Researchen_US
cristin.unitcode1920,12,0,0
cristin.unitcode194,66,20,0
cristin.unitnameKreftklinikken
cristin.unitnameInstitutt for fysikk
cristin.ispublishedtrue
cristin.fulltextpreprint
cristin.qualitycode2


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