Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/25848
Title: Is adoptive T-cell therapy for solid tumors coming of age
Authors: Pedrazzoli, Paolo
Comoli, Patrizia
Montagna, Daniela
Bregni, Marco
Uludağ Üniversitesi/Tıp Fakültesi/İç Hastalıkları Anabilim Dalı.
Demirer, Taner
55393694800
Keywords: Biophysics
Oncology
Hematology
Immunology
Transplantation
Immunotherapy
Solid tumors
T-cells
Epstein-barr-virus
Activated killer-cells
Lymphoproliferative disease
Metastatic melanoma
Nasopharyngeal carcinoma
Successful
Antitumor-activity
Phase-i
Lymphocytes
Expansion
Issue Date: Aug-2012
Publisher: Springernature
Citation: Pedrazzoli, P. vd. (2012). "Is adoptive T-cell therapy for solid tumors coming of age". Bone Marrow Transplantation, 47(8), 1013-1019.
Abstract: Among the novel biological therapeutics that will increase our ability to cure human cancer in years to come, adoptive cellular therapy is one of the most promising approaches. Although this is a complex and challenging field, there have been major advances in basic and translational research resulting in clinical trial activity that is now beginning to confirm this promise. The results obtained with tumor-infiltrating lymphocytes therapy for melanoma, and virus-specific CTLs for EBV-associated malignancies are encouraging in terms of both ability to obtain clinical benefit and limited toxicity profile. In both settings, objective responses were obtained in at least 50% of treated patients. However, improvements to the clinical protocols, in terms of better patient selection and timing of administration, as well as cell product quality and availability, are clearly necessary to further ameliorate outcome, and logistical solutions are warranted to extend T-cell therapy beyond academic centers. In particular, there is a need to simplify cell production, in order to decrease costs and ease preparation. Promising implementations are underway, including harnessing the therapeutic potential of T cells transduced with TCRs directed against shared tumor antigens, and delineating strategies aimed at targeting immune evasion mechanisms exerted by tumor cells.
URI: https://doi.org/10.1038/bmt.2011.155
https://www.nature.com/articles/bmt2011155
http://hdl.handle.net/11452/25848
ISSN: 0268-3369
1476-5365
Appears in Collections:PubMed
Scopus
Web of Science

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