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Title: | Programmed cell death-1 inhibition in lymphoma. | Austin Authors: | Hawkes, Eliza A ;Grigg, Andrew P ;Chong, Geoffrey | Affiliation: | Monash University, Melbourne, VIC, Australia Department of Medical Oncology, Ballarat Health Services, Ballarat, VIC, Australia University of Melbourne, Melbourne, VIC, Australia Department of Oncology, Northern Hospital, Melbourne, VIC, Australia Department of Medical Oncology, Eastern Health, Melbourne, VIC Australia Department of Medical Oncology, Olivia Newton-John Cancer Wellness and Research Centre, Austin Health, Heidelberg, Victoria, Australia Department of Clinical Haematology, Olivia Newton-John Cancer Wellness and Research Centre, Austin Health, Heidelberg, Victoria, Australia |
Issue Date: | 1-May-2015 | Publication information: | The Lancet. Oncology; 16(5): e234-45 | Abstract: | Cancers can evade the host immune system by inducing upregulation of immune inhibitory signals. Anti-programmed cell death-1 (PD-1) monoclonal antibodies block these inhibitory signals allowing the host to mount an immune response against malignant cells. This class of drugs is active in solid tumours, where upregulation of cell-surface PD-1 ligand proteins is nearly uniform. Because lymphoma is a malignancy of immune system cells, the role of the PD-1 pathway in these neoplasms is more complex. However, early clinical trials using PD-1 inhibitors have shown significant clinical activity in various subtypes of relapsed lymphoma. In this Review, we assess the scientific literature on the role of the PD-1 pathway in lymphoma, the relevant clinical data for PD-1 inhibition, and future strategies for this next generation of anticancer agents. | Gov't Doc #: | 25943068 | URI: | https://ahro.austin.org.au/austinjspui/handle/1/12781 | DOI: | 10.1016/S1470-2045(15)70103-8 | Journal: | The Lancet. Oncology | URL: | https://pubmed.ncbi.nlm.nih.gov/25943068 | Type: | Journal Article |
Appears in Collections: | Journal articles |
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