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Adoptive cell therapies in thoracic malignancies

Cancer Immunology, Immunotherapy, 2022
Immunotherapy has gained great interest in thoracic malignancies in the last decade, first in non-small cell lung cancer (NSCLC), but also more recently in small-cell lung cancer (SCLC) and malignant pleural mesothelioma (MPM). However, while 15-20% of patients will greatly benefit from immune checkpoint blockers (ICBs), a vast majority will rapidly ...
Julie Lasvergnas   +5 more
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Adoptive Cell Therapy

2021
Therapy in oncology has undergone a revolution in recent years. New biological agents targeting specific intra- and extracellular domains have become standard of care, immunotherapy with checkpoint inhibitors revolutionized therapy in Melanoma, Renal Cell Carcinoma, and in Non-Small Cell Lung Cancer and combinations of both are now entering clinical ...
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Adoptive cell therapies for posttransplant infections

Current Opinion in Oncology, 2019
Purpose of review Viral and fungal infections cause significant morbidity and mortality following hematopoietic stem-cell transplantation (HSCT), primarily due to the prolonged and complex immunodeficient state that results from conditioning chemo-radiotherapy and subsequent prophylaxis of graft vs. host disease.
Gaurav, Sutrave, David J, Gottlieb
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Adoptive cell transfer therapy for melanoma

Experimental Dermatology, 2022
AbstractAdoptive cell transfer (ACT) of tumor‐infiltrating lymphocytes (TILs) for melanoma is an example of the most successful cancer immune therapy. It achieves a durable complete response about ~20% of patients, and they might be cured. However, the ratio of patients with durable benefits is not high, and its complicated procedure prevents its ...
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Adoptive T-cell therapy.

Seminars in hematology, 1999
Adoptive immunotherapy, or the transfer of immunocompetent cells, has been shown to be a promising new strategy for treatment of a variety of malignancies, including leukemia and non-Hodgkin's lymphoma. The possibility that it may likewise benefit patients with multiple myeloma is now being explored by researchers in Europe and the United States.
Lokhorst, H.M., Liebowitz, D.
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Adoptive Cell Therapy for Metastatic Melanoma

The Cancer Journal, 2017
Adoptive cell therapy (ACT) of tumor-infiltrating lymphocytes (TILs) is a powerful form of immunotherapy by inducing durable complete responses that significantly extend the survival of melanoma patients. Mutation-derived neoantigens were recently identified as key factors for tumor recognition and rejection by TILs.
Efrat, Merhavi-Shoham   +4 more
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Adoptive T cell cancer therapy

Nature Materials, 2018
Tumour heterogeneity and off-target toxicity are current challenges of cancer immunotherapy. Karine Dzhandzhugazyan, Per Guldberg and Alexei Kirkin discuss how epigenetic induction of tumour antigens in antigen-presenting cells may form the basis for multi-target therapies.
Karine N, Dzhandzhugazyan   +2 more
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Adoptive cell therapy in multiple Myeloma

Expert Opinion on Biological Therapy, 2017
Recent breakthrough advances in Multiple Myeloma (MM) immunotherapy have been achieved with the approval of the first two monoclonal antibodies, elotuzumab and daratumumab. Adoptive cell therapy (ACT) represents yet another, maybe the most powerful modality of immunotherapy, in which allogeneic or autologous effector cells are expanded and activated ex
Sonia, Vallet   +2 more
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Prospects for adoptive T cell therapy

Current Opinion in Immunology, 1997
Since the establishment of methods to isolate genes encoding cytotoxic T lymphocyte defined tumor antigens, several antigens have been identified and characterized for suitability as target antigens for immunotherapy. The development of innovative strategies to generate T cells targeting these antigens and lessons learned from clinical trials of ...
C, Yee, S R, Riddell, P D, Greenberg
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Neoantigen-Specific T Cells in Adoptive Cell Therapy

The Cancer Journal, 2022
Abstract The holy grail of cancer therapeutics is the destruction of cancer cells while avoiding harm to normal cells. Cancer is unique from normal tissues because of the presence of somatic mutations that accumulate during tumorigenesis.
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