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Current Immunotherapeutic Approaches in T Cell Non-Hodgkin Lymphomas

期刊

CANCERS
卷 10, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/cancers10090339

关键词

brentuximab vedotin; chimeric antigen receptor (CAR)-T cell; checkpoint inhibitors; monoclonal antibodies; T cell non-Hodgkin lymphoma (T-NHL)

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资金

  1. European Union's Horizon 2020 research and innovative program under the Marie Sklodowska-Curie grant [675712]

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T cell non-Hodgkin lymphoma (T-NHL) is a rare and heterogeneous group of neoplasms of the lymphoid system. With the exception of a few relatively indolent entities, T-NHL is typically aggressive, treatment resistant, and associated with poor prognosis. Relatively few options with proven clinical benefit are available for patients with relapsed or refractory disease. Immunotherapy has emerged as a promising treatment for the management of patients with hematological malignancies. The identification of tumor antigens has provided a large number of potential targets. Therefore, several monoclonal antibodies (alemtuzumab, SGN-30, brentuximab vedotin, and mogamulizumab), directed against tumor antigens, have been investigated in different subtypes of T-NHL. In addition to targeting antigens involved in cancer cell physiology, antibodies can stimulate immune effector functions or counteract immunosuppressive mechanisms. Chimeric antigen receptor (CAR)-T cells directed against CD30 and immune checkpoint inhibitors are currently being investigated in clinical trials. In this review, we summarize the currently available clinical evidence for immunotherapy in T-NHL, focusing on the results of clinical trials using first generation monoclonal antibodies, new immunotherapeutic agents, immune checkpoint inhibitors, and CAR-T cell therapies.

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