dc.contributor.author
Comoli, P.
dc.contributor.author
Chabannon, Christian
dc.contributor.author
Koehl, U.
dc.contributor.author
Lanza, Francesco
dc.contributor.author
Urbano Ispizua, Álvaro
dc.contributor.author
Hudecek, Michael
dc.contributor.author
Ruggeri, Annalisa
dc.contributor.author
Secondino, S.
dc.contributor.author
Bonini, C.
dc.contributor.author
Pedrazzoli, P.
dc.contributor.author
Universitat Autònoma de Barcelona
dc.identifier
https://ddd.uab.cat/record/237065
dc.identifier
urn:10.1093/annonc/mdz285
dc.identifier
urn:oai:ddd.uab.cat:237065
dc.identifier
urn:scopus_id:85077172937
dc.identifier
urn:articleid:15698041v30n11p1740
dc.identifier
urn:pmid:31435646
dc.description.abstract
State-of-the-art treatment strategies have drastically ameliorated the outcome of patients affected by cancer. However, resistant and recurrent solid tumors are generally nonresponsive to conventional therapies. A central factor in the sequence of events that lead to cancer is an alteration in antitumor immune surveillance, which results in failure to recognize and eliminate the transformed tumor cell. A greater understanding of the dysregulation and evasion of the immune system in the evolution and progression of cancer provides the basis for improved therapies. Targeted strategies, such as T-cell therapy, not only generally spare normal tissues, but also use alternative antineoplastic mechanisms that synergize with other therapeutics. Despite encouraging success in hematologic malignancies, adaptive cellular therapies for solid tumors face unique challenges because of the immunosuppressive tumor microenvironment, and the hurdle of T-cell trafficking within scarcely accessible tumor sites. This review provides a brief overview of current cellular therapeutic strategies for solid tumors, research carried out to increase efficacy and safety, and results from ongoing clinical trials.
dc.format
application/pdf
dc.relation
Annals of oncology ; Vol. 30 Núm. 11 (november 2019), p. 1740-1750
dc.rights
Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, i la comunicació pública de l'obra, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. No es permet la creació d'obres derivades.
dc.rights
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject
Checkpoint inhibitors
dc.title
Development of adaptive immune effector therapies in solid tumors
dc.type
Article de revisió