Clinical landscape of macrophage-reprogramming cancer immunotherapies

dc.contributor.authorRannikko, Jenna H.
dc.contributor.authorHollmén, Maija
dc.contributor.organizationfi=InFLAMES Lippulaiva|en=InFLAMES Flagship|
dc.contributor.organizationfi=MediCity|en=MediCity|
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organization-code1.2.246.10.2458963.20.68445910604
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.contributor.organization-code1.2.246.10.2458963.20.83772236069
dc.converis.publication-id454779913
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/454779913
dc.date.accessioned2025-08-27T23:39:22Z
dc.date.available2025-08-27T23:39:22Z
dc.description.abstractTumour-associated macrophages (TAMs) sustain a tumour-supporting and immunosuppressive milieu and therefore aggravate cancer prognosis. To modify TAM behaviour and unlock their anti-tumoural potential, novel TAM-reprogramming immunotherapies are being developed at an accelerating rate. At the same time, scientific discoveries have highlighted more sophisticated TAM phenotypes with complex biological functions and contradictory prognostic associations. To understand the evolving clinical landscape, we reviewed current and past clinically evaluated TAM-reprogramming cancer therapeutics and summarised almost 200 TAM-reprogramming agents investigated in more than 700 clinical trials. Observable overall trends include a high frequency of overlapping strategies against the same therapeutic targets, development of more complex strategies to improve previously ineffective approaches and reliance on combinatory strategies for efficacy. However, strong anti-tumour efficacy is uncommon, which encourages re-directing efforts on identifying biomarkers for eligible patient populations and comparing similar treatments earlier. Future endeavours will benefit from considering the shortcomings of past treatment strategies and accommodating the emerging complexity of TAM biology.
dc.format.pagerange627
dc.format.pagerange640
dc.identifier.eissn1532-1827
dc.identifier.jour-issn0007-0920
dc.identifier.olddbid204370
dc.identifier.oldhandle10024/187397
dc.identifier.urihttps://www.utupub.fi/handle/11111/52582
dc.identifier.urlhttps://www.nature.com/articles/s41416-024-02715-6
dc.identifier.urnURN:NBN:fi-fe2025082790412
dc.language.isoen
dc.okm.affiliatedauthorRannikko, Jenna
dc.okm.affiliatedauthorHollmen, Maija
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA2 Scientific Article
dc.publisherSpringer Nature
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1038/s41416-024-02715-6
dc.relation.ispartofjournalBritish Journal of Cancer
dc.relation.issue4
dc.relation.volume131
dc.source.identifierhttps://www.utupub.fi/handle/10024/187397
dc.titleClinical landscape of macrophage-reprogramming cancer immunotherapies
dc.year.issued2024

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