A Phase I Study on Adoptive Immunotherapy Using Gene-Modified T Cells for Ovarian Cancer
By M. Kershaw, J. A. Westwood, L. Parker, Gang Wang, Z. Eshhar, S. Mavroukakis, D. White, J. Wunderlich, S. Canevari, Linda J. Rogers-Freezer and 4 more. Clinical Cancer Research, 2006
1,238 citations recorded by the source corpus.
Subfields: Genetics, Immunology, Oncology
View Paper: https://www.semanticscholar.org/paper/220272aef3989d11f747d8cb1038031acefd4746
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Citations in the corpus
- CD28 costimulation improves expansion and persistence of chimeric antigen receptor-modified T cells in lymphoma patients. (2011, background): “However, in the initial human trials, T lymphocytes expressing first-generation CARs showed limited expansion and relatively short persistence (3, 9, 10).”
- Distinct Signaling of Coreceptors Regulates Specific Metabolism Pathways and Impacts Memory Development in CAR T Cells. (2016, background): “First-generation CARs consisting of the cytoplasmic domain of the Fc receptor g chain or the CD3z signaling modules alone, often become anergic, and do not elicit potent T cell antitumor effects (Brocker, 2000; Kershaw et al., 2006; Lamers et al., 2006).”
- Tumor regression in patients with metastatic synovial cell sarcoma and melanoma using genetically engineered lymphocytes reactive with NY-ESO-1. (2011, background): “However, no clinical responses were seen in three patients with renal cancer who received autologous T cells transduced with a CAR directed against carbonic anhydrase-IX(18) or in eight patients with ovarian cancer who received autologous PBMCs transduced with a CAR directed against the -folate rece”
- The Principles of Engineering Immune Cells to Treat Cancer (2017, background): “CAR T cells targeting folate receptor 1 alpha and CD171 in advanced ovarian cancer and neuroblastoma did not have toxicity or efficacy; however, the short persistence of the infused CAR T cells precludes interpretations on the safety of these targets (Kershaw et al., 2006).”